[![English Jobs Logo](/public/img/logo100.png "English Jobs Logo")

### ENGLISH JOBS EUROPE](/) [post a job](/publish-job)

search

# 8499 English-speaking jobs in Italy

Include languages [+]

### Note

Some links might not work from outside the European Union.

Dismiss

[### Clinical Research Associate](/clickout/770b8d35b89fd122?ql=l&sig=ceb5e8556fa261efe465bdb84cdc4c4097cb0eb2&e=fp_Qqpem732pztgoVEwDS3Rr8CeXhilxztzQFeE4ypFf2X6EeESUqtEo9tKrngVQDgsqs_dS6p6KYWmxtX1bQR85dwWbdZxT1EQfbYuzw_GAdBqeYzqFI9SY_dnccdjapzU0WzJPCAKfbbk8v2i3pr2tLywUD__jGMQZNROa9DcxvWqOnLpoJYdPVi-uC3M6rmQ1tKvpePb-KrGBFiXVPi4aW_EpJfebXr-hSBNITp8I0AwuMXPzj6tn7OWRe-GAKUNGnAM9gmKf2aOt1L0pQ4giovrusHYdVxU-UWpSCjS4uIXpnv-FvVYNZBc2WlF8yqPkAlxHLXT-4AJ9W3EQgfd89Q3Ei56biq-bHh1WOD4OjbCPztdHITriaXZwiH8lplNWJVbuOCbsyClserkEgfb-d3VYGT-juFiEM7usW5c93WPHNJITF8069guPvuHXqcQpzGZEQTq_BcEyqUJNGO5prXZ6hkaeUCXHTVmMGCs0z-4bj7I5lkT48kgSqjSTjOU7Cf7cj4_u_BLx9jRjqneO8RLEXNYyQ-LqbiYlQWKBGmn6e3O9NV9YaNgX0mon_qwVjyjPa6tE38v3MGWhddLFAcyA94TlFGFhrw3ojVQK5y4MkNKkpzuRfkU3Pwpht8brog7TURprPRu8ftxdN9L4WX711ymJxYotVt4bcTTh8b-ersUmnZtVT-0JoDuoSU9zPrlrXzmqa0cocEhWMqTnwES4KVTY4bd4caJGsBlO1aJBDge9_BLluL_xo0tZRc4cMLQQUZG9aNgUoVhhLK_MZeRoDLJ7f5hLk1vyUGOb9zrH1jpLrx2bZ-PMzWBfiny30f4m4F-aU1GOXUb3-hmEisVqN7eJ_TXgQPTiN6tbooyi6EQPJmKMcopMkGwxF-3LqJPF-L6o-LgzmEMj45wCdEA3dre5eRIf6t0Z0qKJiQevTT6rPWw8DcfcwWa-QopNniwLNO3NPTVTCFl4pThiyUHuTBShiROJgWEYeQb0r72XJCep_5Ze3KF2KAi7k02b6WbUT6PaJjJg_EoIzjY3gWiEV5q1Mt7GgTSsVY4t25xLReZmsEVsu-nX5eWIF50o-Isrq-1Dn8ueAWQtPoQWr8QV5YZYeEdxv1PIUribKJD41Be9-52UAzH1mgIjRLGjne14e9AgIEeXncZbQBVfsyHRmmRzNaxYjCmOQC_oJFSMTJUlYCjWobcLfflw7jrsjaqnL189QgzfQixlp-KxAvtzenkH7SMIW0ifnD9yQL3ypjSaANat7DgSyTDK1rT7SaXKwHhEIYakHG1kEHqwdGlsO_r3qWDl9k0n4F8nVrCQGO3qmya64CVG_xb4rcjS1s840cEk4JlYdjjrnfUS9_dqoelye9fpE_poHhp62y5vichHjYcGNyaL2RkSN7xm6mczgRwWc6-DfVnyAyMzSJ5eU45MaMuX54oo49ZZVnUXeFh9-bpqI2wxZ3iyAid8_T-Ahz6MPNBTnb4z_P5g&prev=RQD0531E8188BDFB&p=1&pg=68)

* Italy
* IQVIA
* Pescara
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/cd7a5d908095e800?ql=l&sig=4cbe9d70773d80327b1e7f9d8dd972f44384d6db&e=6ORHjRU481p_encnA2CEFIcgaT5Q8apL1cCL_45mYxKk3bhsQiifDfBCsiSyzGi-xu1eE74hy9shryVqIpkQKo7sWqxc9uMGOtWIEcFWxdnYIF-9f_MpAJCrttxfikv59Xdia-xfcKX_KKyrpJvL-YxGE8RQ3pe6J9vhcKAaI2HfuSPpZwnfyXzV1GruT5METucDgSG7d2zGBvjLP-5_hPr6619qwMeXveEySLSdmHS6PUc12suvWMG1ZvxL5hZWHx4qb6W88pCShh6E7hvpuT0GfVRs1mOWKyU3tuTw2TBiYoFVh_tU-C1iO7qxj8eOmOqt6WIA-Ap6J6Yy9vgWscu_0lneJNJyjwPHQhMWYJcpS1ErR3Y-QDH8q6_pR6Qhy1WjVIBwOBWO-mnTqnx4UYNJpX6y0WPWerJ47gmdi_GPVq968bUmyWdC9x5jDP7JOpTYuf27iLMQ23EIsLI174SoLrPfHuhtaeyApiaK5MhYcvGBuG7C-xVnEtMUNNmd_97SJ_uL54q-qOcFGJYZ52vehmBvLjS3JrV54u9OgcfVGzAvGPQa85tI2AJEwR9n0SPmDYyIDKuNFLOaHo-s-JZ1y1ZFW4M2cDScUrDtF-MdcSdiuWtv1MrFxA0zwMOKG7gUKwHl46LMBn5dg0T3zuTQejXjuQoFWOxM17yvG9SsAAiFv-LFr9v_-lszX8CMYU-LoM9EiQiRomjulTbysKpAlUqDhyDZwBjqofekpcd4_KdLU0TaHFRs3tYBlcN8mb0IrVmrWLSpXy7WvNVxSkbByrRvC6zHxEFDl9kn8d3ZYh6KNZc3MbI7Y6dvTXnBtzobe3qTma62R7FU2hml7WCHMlGoYfYCOIpInj612-0r2KzGxz7oRl19uRPmezEZEwRg-FFfnNlQ6yJgxItfZpVAxfewFVQWyOBpYiEQr3r969IJXoXvxuoGeK_jv8NHLzFKC9fTMP0D7_XUlEPpRiDLLeHXvQXbMb22xg5SmpqgNA9pyYAdJEe3uxY4sLUMmzISoIdIeUfnM0b1Hxv9UlmJ9RmkzrgVt9DRfWbMb7LCOljscI2Tb6eg-he6k5Sg_BjpG6q8tZ-km8jlG5DwRjOIGErfK7KYQBDAPt2GAFk6nsuI2LO4JIhMWIym8earSiv7f--yGft5Q3VYNY1QJkjHWizcev4wsbiQ1jd4ZaOf39Knlw9s1nrTAOjmsyfr_zQkFPdSxUpjnae343tbEOX31WSdmOpMlDx0sWY5Ex7AmLU_RJ_Qk3_fL5MEV9UnZP8k5mXEXRTir078AgfVL3L-prl3a_ye6ihn2fYTORpMw8UCOhcIlO63BgMRgJ_oMxSgtkohvJgCsBY3QwHQQMiCjA5ZYH-Cd_LXG84ZkXZ-1TYwEUbtT74RHi9p_2h2rtU2PrltQqI6OvJM6bzlMxa1UEXGryZ_rJaGQCljnVl8DdIpOQi8WD8c0gJE9Ew0Wh5HfzbwkqrAe2gFcHGO8iDP&prev=RQD0531E8188BDFB&p=2&pg=68)

* Italy
* IQVIA
* Livorno
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/ebc20963688910f3?ql=l&sig=6b73f3c802f8ecdb338a3b975f6539ccecdeb61a&e=avE4JixRZRe6d_ysAZmZzwoxIBriWSbCbO7-u4pnOXxIsJsaGU1lQ_gnE5XoGuYdM4CX9n9fmfOhtIj2kAWdtMKWojqeIk6Z8e3b_3TnLh3Zdbp_Xeyt8thq3skPtkwIWZLnKrEIl7gn9q7pyZQfYR6UIMWb0mZaOibteQ1dYDHl4dj4ShNL5EynEfTSALYOUJqTsPAY0N1C1lD2ESUrK1TnlGBRDVY8CqqSXDY0FJ67hU3nqJ93iGipG6mBwxOCzagwZ2wBqEjgT7_pDPN9rpqbh-v7f36NH77D_SHjZL8VwXBq3UHatKC6CTPLG7ER4pSsTo04ZOptWClXUE-4gxo50POzkB1_mIIEDOxgiEwI1VFPF3QuIr8m_wuOE-9Zfy3minVnagH-u5jvZtV2QBmUVssjaeTkOYZE5tR1CJvpWLJJevPs0ityi12v1RB9A1--4PCwYyXdz9RBnGaA53i6KB0kY3miXq4vj7UxXC9MvPkdqcqGwT-hMC3nG-lLEXrvO3OK7VamJpR3nl1asT3sQtg-zhbn3C1oY4r2_LTRQYDtC2Ehl3fek53evdQDlz1f0d9KEbGHlXFYkRhgU5r15a64eRIn3Gl9E9soBZ65C04jEWtWxrMy-SwgwGgrTvzLcthCWxK5XBZFzhGu49B4WvTOq6keC5OTO8CWx6qwVd_PpDfnqxjtyaZJE2PLSE_LST9ZqpV6b0Ap65QtNzSpTICBihXdVmAz4-cra9TL3jhrM4xbnvXmpwQeBNq697hR7VfSbhtzC5C89HJN3w5EuwVWncCTLrQdjT3esMq4FcsiFoIHYo9USxuWv6MM3_CP_rcayUxaRpno2DdX4O8ZddJ6ZcFakYxHmcDC2NdBg6EzkXVNan659jqpAmOC0iDLrro1HEcy9iMaTtR1VPU76oJqPakqjUu6F3yx4GIzur57UEVnH8HcuGsU1yaZCaQ2-nhrREnhCE_bOdaJ137oB8-1OBferrkVBvwmKi5GZT4LzYhNm7XV9IqdaHvjBmtn8TYb_R2N4L44cbWXoySX4pDQMzpcvBALb6iEfFWJ2Kz7YvRGMS_8x5Je3KxiqPBQd88cOKLVwgk1LXBh7DReUftQmdQl0v9V9ErV-MdfmMApXeeMGXrlrodP02r4kf9TJWDx51mck8sARmKxtHYRZsnFXKqGY9bV1dOzFfOI7H30O2lFQinzzzCgT2f7zTLbWKutN2vLmjPU5dw38k3k38pdt9Y6SuS_8nMepKdVyT3HFZez8UgXTWMwhxPYVuIQmHh-UWIywOWm79aW4-vvDY8Bo92mSyCzxRw1xMMVOG72Krk2BcNr_GnLVdxYZo9wgCr-7Lq1szO4apZf7YfPCctNItlUGHyojLdPCnMvCavBibuiQFpv7c0KS9y8oLIhgTryiUrK5OKhymmRGgISC3uuQ9TCs3949nlhjHRUOTQY-j--ySHXLGFVApd_AG3hdshp3sh3jhhwogAoi30xLIyo3A&prev=RQD0531E8188BDFB&p=3&pg=68)

* Italy
* IQVIA
* Alessandria
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/b0658c41c70f7fce?ql=l&sig=0dc84a6b6e9de87091a90cfb55f6bac2fc0ef8a7&e=jvheKOUKhU5JVqjcmQHW1M1wwdi6nt3Z_nAPXSmdgN6gC7w9P30Kpib96jILJZ5WI7Q7QseAXs1i8EZfxGwvHorvE0uM_421dWd9B-TDKhOqbg-xjiQHs2qpkCJZODlAEWLyvKa5FEzKjXQ6I60D4KX5jJE7zS90eUdSf5BJoIbUuaJXjKd34Ix41zQMQ0B6Xz1KfkDVZnd89waacsqI1eQGFCQiCX-xzko7uw0mrKDVYfJvOwMbXBs1WDbZrGOoPdZfd3i8YB8VGKaQ7uDe6qT7_nCX3ZOs-_I5aSToza4wavAlypdkmwuJCWer26A3FdvYwBi6LvijvfdinjvDG5vprKnw5BRS3AcyErsdSVMbbgOIS1vN9I5P81C9MOiyjRYw9t3fARR29Kgx9mGW4omKxq3KqgN30uTETrwYjGrtKF92Ms36alzSG-iwEVlXWaNzh5jFAUQPe4VQ1BtJd9twl8dD2BPFBh6nvI8Ge07sN7hT4bl9SmGkLMkohOVha5JuDmUKkh7clOB3Y7y-vRre6TncIrJzBRpBNlQcOfFSLvo6iMyQaP2tFW5me8CEMAn922BV0N8ir4mfi9K7LRtQCueAcq1IammtZsXhqcpo0qoqsJgERGPCsT5OPz2u6VQk8XNEW4uAwDCUIb_vabwXbtz4mgmEaOorqwc8e-cIM5wVY7vk1e7Xe8Gc2tSvq-RmTOeFcGb6-WevS4eXy8S3GFHciEOaHeZrLH4mCim_fxu7RnjcUgSVfI8omU8Jk1O5HrkEzc7GPs6zXPv1REWYh4Yuh7JAuRxEV-1RDprY_teT111-gTUBhCjSNuhxHiUJCCVzqAE6KKAQ_8T0_irDBv_5n3brLeeicndi71Y8_O9_QY-ml8UNCwGG0V0j-GTxiJ_6HJTuvigP7FJMxb3dBSF00GBBKVzcTjGPRkYlmv440NjewvKhO3NTCBtBnJRD28wygDaBFFD0KwDFJ48Z4n5v7YNsU4e_pak8uhch0fVwzxN6xUW_iT_a8AXPIhRpTFGOVr5WmMB3ovBoBYT01QIKBDhG1L2uUHySt2Aqn7_R62Qb2qqt_iGHKlPZUPkB34kYQ9KEY3V1RXD60PmASo0q_KUMOd1oXxlc6To0RIS6KnjeuN0r-trBDlBVhJQA9K7S7fjneE8RjjN8mbP5T58er5322duhaCpEvOaGBLYFYoM8786DW6wqR9YbJ8Yw7OSc5oEX7Y5kIhg7vMjdlUwqd7J7mjzPwjek7QyQ4Xre76IPl5a00DfApktrVpdmi25nY3y3lFoS3OTS2dDFi1MYi11r022PBri3i1qdImW6V8ooxDj54bKbBr89Rc0k4MrcvuRwVokYMhoX9OhcWnxcuI03D-qPWq_Sp5twbn3AQmAod4brJq27hAL5fCnTlwB5NhW178IeqlUGMRvkFwp_wbvfw1Q2g9T8tXdkZL753VEUJzRS5GComLVGqc2Acusdgw6R_hB1laMOSA&prev=RQD0531E8188BDFB&p=4&pg=68)

* Italy
* IQVIA
* Lucca
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/2ba983391680a966?ql=l&sig=b42998f32e2f2d81387425fd4b6a7fd748b9bf2f&e=RnZAJGvDI707hOcbeRSwoowkcUULs902pTvA5x-nrq0SsP6R8s_4uPASEZ2eXc47WDzQfRYVXbpN5VLDNxNG3scrj8HTls7QohMb2VhKq8iQdtG1VDHO6XlAZCz8J88bDINDcEzcbRQPZLnL_mePpXOSXmv1ca17yeXbLiH3p23WVblYR6N8GR1jV-ESeNSG1guu3WLRxcOVx0HEFJTQOuak7aO0wqpdWf7h4ZIMpmRauDG6ao_IRqLkrdA1c6xMDi8hOp9CSgOlrh_jpjVt-WoVPSOIRnMEM9ABInpO4CTg6XfSEhFRuN8CfMUULQ6RuYhGWLF9qdh5yySDSrClbgDr5ut21f1U9W0pft9izKpexk-ofmQm7E8_eNcZn_5nCDI8gyXwhyGpOZ-CGwS_ZZOJ5tXzBVw-sAyhVxSFlDpdKV9KilhbtvcT_y2lYt4jnUCTSTaoQNG6HXsC3XPCazuoC1d3HHcxKENigVonZxRmf3jUvsKG9p8gO1szt8o8EsmXM93qX7Xj82hCI6EGGpLZZq65pgSDHu3H5_Epby86dKtPIz2x5T6V6rnta8SSiZEwRP8XghMevyosO0uIchtBKHDBwILKiUg-NYknJbLkeXo_eFxFWFq73jvfsaZSKc9TIgSlmS8HgoxG0XfFqYn2D20sKt3fkuNtXdvioBpotN0-fFAhU5g9bMtykJ4rch11beJmipZYw17ft9oWLhL58SW1VJIM9QPIXAhrDni_uWkHnpEyswqyzXw3JPq6R13XT0a9lNJP2S2EB7viwWmiOF3JzgrO0tS2ZTo1T5knLVaAFNVH9mUBN3AS5uUgMkXRqD64UEnviJ-lqAufiHNQ_5Fm6QMp1pbSBxfts-h2SFV8C9tJbcfmaXJ0mcYlkz_2ehm8BKEj77B4HluoCb_gHtPMZ1MHWaTAd8M5kOI4CYt6eesBH8_Z5KGu9lfyhcaDj-gUmic6-0ChM7f_Zc-g8MdWdaIPxsbTWKna2j5PEUogjSIQTceCWlcmZRvfq8oaP8Lc-3WNtDFsuOwSrJMrj5eGnlCsOrsXrQyP1cwY1NEysHE6rSj3pvjtCP07bs4V3LjpBM1cW8f3Bm59VErsDAElUDEIeUhdxZFEbEQC270ouI7QMKZiOBR3Cg-HyLoJZbUMYbedX3ePPaAALOoYMdjkimary0lGcZAOjrTn69JumT2CG0B92nVZ3P6RrOqqCrJ44trJdu7DNisM2QHoOxtLuSLTw0qzmUYbxruGpAYyE1RfGnpjMqsW-BUQm-0Kug5c3Gcdv-IgbhH3_tPiwIbCqeMLbHoz-vhd7S-XlKpQHFzfRAlj0XyDvB7oMasx8R0rSYU-cqzw-4ZRzHqLV2IsSjzsjLx3UoY-PUJh14OSFAuby_KJJy15654q7D-0rd1Kh9CzxeMUIWHK-JbIVdDtKbzQenANs8ZqQFXBQKrQwKcEmomagdOzaMxcBkSdu2-TFBWu-_Q1g5yM6yFc&prev=RQD0531E8188BDFB&p=5&pg=68)

* Italy
* IQVIA
* Caserta
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/e5a2fddb4a354b91?ql=l&sig=f670076dbe28767edeb9275ba681310b659667ed&e=4IUqB_YNsU7viBNimOWiu81VmEfLbgs-tNJ7K8gEdVpcSjwOAzLdaypf1J1x4xpIpIKEwjRqHCWNp8214oE6ikC4f09MDuKPopYPI1T7_u94WMOIAP42DV_1GI-JcixxV2dFSouIyRRNr01ptPtwWj3TLRIGbLb56lAjl9x7BfSX9Z9CAu09J2N9Lai4z5_KOEwKiWdZd-02nnuomxCqsRR5crAsWa87r0BXa9OqG64jTvGZ3K1pW4C1MG5wLhHCIw-qU1fKSpSgD0rbt5VoJnv_ftNNt5KTDjbkeI3MJypf7yqEQ7HjYjGegqYqEr-F2ORphsMWwaQrlw6fzu8-C21FPJ-IMsY4h2pB8hp8U0j9fP8klKI3Cssy8eOpH8b874fVwBgvuKJawIIAB2xqSuUQ4gwGKJb03AJYvGAz4ewZu3GUJLjfNh0Evmb3Woi5QQIETGP8wCV3alh4ZTNsK7Loejgfwrbsz-9GtwPtLJp9x4z-9vZmpEA4nPnzrigvcsTXkxrAsq_dfUHS0VoOdOqjtp4897Nwd6XE4Hp4gED9k8reSUlVMNc2FKHqs8yVbiFUj_Dz3utEdI2HVlq-19OI3oON0n5c1xzM7n2QPsmDyAqSWqP0IpYTYvAgPVGt07aqBR7JGOb6basulaZhp8Y6yGCYqVQCda6MRcRMjnjo1pOthna9RB_pzOQJ90G2K7vT12ZFKyj9QKaOyJQGap9GzgVV6uucOvexY-z2UPbYaV7hqwr5jdrLAT0c2WqgfHK8-io4dfsBpQiTiOYmfvvUB8FUviL-I1Yt_taf0lB6HdT4MR1gBpDngIjPTn1DJG2TCb3tWCPn2DeJaLC9S6kG5n3yrt8PwQLAarBwWrWcZnn3J9jUIB1BA7wxJpie56WNm7nU-yZLttW-CeBq7HUVfEh5P5NShWxR7owjDMIVCNAcbjf2NBp9xXsyPJowLYvNg_I8W30TGZX_9Lq4bfhVal0kMtWiFkxHl1M_URyFBGp1-A8ggReqRQmFcNUxVTLqTsfq_6Ea04KHFNtTSwLW6bGz_lY0Qvxqu7VMRVo1kTcPLbE6geNOAg0nKQjKx6YPbSqK7mwUcNepqZE_iNnoFiZ8tFeQqlxV5rp3DXomPXhia0EP5VukKy_SfJF0q0HlKvDRZioU9QJ21YpZBHZJL_B_F5t2dBiN-X-l9ejDYGSmXPR47Aq5YYu3K95_Y36GP1P1G3ZveaK5baC1STmFM4d9CdniRAAqkaQXuD-9AvMIGO5NVuseXwdN_MijP3xEpvfG1R6LSjlYl5OOoLhlDS8KrRcbGaQPxTU2xc8i2S65nj-K8j2IJNvmRGBhC2LqO9vn9N68A9ny89Tsgav5cwdDC73NXz3jveMaakB1NtD7rCi46HMGHgfxHEWvGVuskgcn4FTOMPGOS_wGlGjx_7kSdKk1cvIJCq-yH8wF-pu-0G_th0LM4FVBvkVVQ-3hqIEDSz1JHO5-tSc&prev=RQD0531E8188BDFB&p=6&pg=68)

* Italy
* IQVIA
* Lodi
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/bfd94720c416e0d3?ql=l&sig=398152be0aff463b121aa7ae2fbfdefb028f891e&e=PLmJ7yKxNzmAAAF8JU5TehUyvinIdZqshgmeUp4ggc9X4FcfcBloIlgVkYqNLF9B6lP-a9w5J4ZSbrvsZfvuHZLKGUPqS8wf6NboMYSUGBi0JOmw4qYTeV-e0ptfQXac6V2N7z5xjKbpzEs842BCTcO74OFF2TKBtVTh67wbL2X3YWtxBh44OszPUcIEJ5bedDW4Wgx2wZIn42kpkkKHaLQVLOawaB5wtHENjSgJINPtAAo9R3nSYd-9sIbli0Jzyj7dLaNd6d0_oKL1fn7AI5bUtBkb4FfBN749L-P1vl9xPux1hQ0q3DMDwrCWemmW5GVYjiRRMxFafQF2k2nrsK-EN1Rb0M_0IisJUVGScdZR4LXgqpqk5u-JCjyjuBXIDVfUX4qec_Hw2J6dciJY6yTXENgrGlzLPzrVTLoWk5bFVpivJuXFAKvZxnpwXaMyytAGAQWtRKK6z0j9Zr3M6RcSHjs3i64QBjyHpIOJft-zWgv_8AsClgvp1QpTLWfOEwHirKsTR3v6l8mvNdJDLEjaPuMbjiZRQDmzl3CgTjuP_DChOMdNI934zQXBePN0GOmXjO0e6oyhtxcEbcw3dGKY4E3L4vjyMsLcnEO6H29xzg63K25NbxajC_eZ6Zir_JeI0W1lHKHe_KpRiPH5TRRBgEFg2_QiYpzv4wLDYouCIKxuPg_TJM7oV5dmvFy41eZRnlZogrYP54b8TXaiaQHxE5GaKLYkw04xfBdYKs-NumUHAHtVFsP8rE5dF_dN5hf21moapq7E4WFapkioQZWnYeNUrKI2z0JFQGn5r884gMZ7FWrMTuhoE9ovF8H5egWg9eju4EYc_jGG4JjIJdrkJmos7AJh7RRZHuHSjxY3F_TbkBvMDMf6pAn1cOKI05D6RprX7EskJO38VEOj97COwbv8S0VNskKmRoU5cTl6PSXJoRebUtJedHb41OXyJQRPWA1M2ego0e9aQshm_8vyBLtuos9P2sylJKczR_gsf5XYSs-Xyn1Yxo-fz-2SnCMxcHE31jcxflHGt6ITMWf3MKeNuIi3mpyRq9WL99IpJ8wgOS3XKdaC7SwDGT9qSBNgM7jGodqNYZXym_15RAULB1FKcL4C8pIxarP5AWe8V0X7N1SEwkm60Yl4s-icm84p-VEC0TB2m6Z1QsfRkwB3RQHkC66R1wrCo_Rl0vsmzzRK8MT6DW3PTJVioN-8_xf5SR9oMQuaPLwWsm7WcCqQf8VDG-4xx1se9Kz-xZ055Qe0sK4oqVjFCm-zO8CNVMH7gBjgkhWR_A5amHfsCy1zTJG9sDmw7CZOG3ZoCVGw5MM_XekrBM1Rpsy4eKcLPJ1nVAVj1c8cL-oQAI4t14htXqKu-CSIVmKo3DB9hQA1ASAslNY0YVMC9Ey9VKBj5QaSrd9PpG_HQHuKl3hIFPi3YN3zjQaax9ddnh6z0BvNh73_to0IAYs_1NysG-uNZHqXEENRPr7OzL_9xxA9zDc8&prev=RQD0531E8188BDFB&p=7&pg=68)

* Italy
* IQVIA
* Salerno
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/97f51248a154cca5?ql=l&sig=f46147a8bb66367a4aae17edd87488cf7470b698&e=gdGV7AGLHEj_9QCW__UsBkJqU0onGGygH-IfillpMBuh-LphrxRc2X-SAq-sZcvPVAZx7Dg3EfkI_-HsmZAuz4SWkjnxcvOX85LFw-yPXnQ6Gv6dsoEFwHW-lxoARK1VWlM1mGdE1cp3iCDNU7JkSNRcwQBIqhZ-LXnq7pQbj9xD5qummBZhrDGfGka4UbcbgzRFzkijbIelplm2Doq_vUN5ut_9fKORgD8MG32Io_3_gE87Kg3bheDV3yzcFuHSgRA5gwQMAbsBauUkKzFoa1WfjW_VIAbxv6Uzr4v2skLa0aIiynnfuMrBIujtCLMy3eflNoT3j8_bAdfFZh7Dsr2rsVyi1oW52nNwZmq0wojU4Cy_Zozgki1Xo85bx4yzGpjbcSWWdGNQ0GRV1ktSvCDi6QpINKqrI3mU4Eg0a0naEIb0hsdeRwg8GSE9KUOsR3XBJD-LQvXzEXjpi3_7e444iEz3L4mIW6dggLSO04OPARUlSW74JJPzJGGRA1OgRvTRO3otxqRyXJmA0LjdX341m9LewH8nbsC_vT9QL9Yqu_wAqrkTQyR6uq4Fe8M3I31GJvq7w7duPyXw_gvN7VNqlIjSWrdmZTxmN4ej1oUfXtqCIULy7lr38rynYRmPxFBh7nzE_aMm4qCXidCIG4tM69dvv7y7XzNiIhpURpeysfpx8DCoxijmf4BH0Qa3iwe8eGpBhjRLjcgdFjPJOzifKS6P9uxj7ce5LU1SGfg5naP63cTcvuD4sRS1hgY0IBGMyFvFhRvZa9uGOhEkLlNUTlCPDtKr3UxjNSDDhfYqKyjYhJPoYhZdQ21OBeZnJXhCyzZ4UbL5X-NLI5NsCsDI1j7_RpKglevV29BRdfOv1K0870d7IrYLnZKiemQDKcvSeGyEluJM_-5gVuakno5LEm68mo_Y3KzKceinv2Z02sFtrcpZaUsk98Bx-PzDEpM1deALhqa2L1_0lxERhfXQUyHKJcLbNHrPhO-6kSNqT_vA6J_M0Nzs7QYJOvYoHYGcZ9H0pDlv-lWQa4KlOiY8AsB8rxxQSUDTkmg8u4HCfcfeLj_RG_swNROuMAMcEgtxQi43nFSPHmD7xmqlt9zdA3cY7Y45P5QTBfhGvGY9VLhnnZm8FT9-f6dkxtDiOj2bwXtp6KRF_4KmNxyvXjYtrUpleq57AmPJhm0mXVPnTsZUIxlltElPhAPBYN-w4d7ITQb99gqdBgPhkXrrSV80yOCuuyFkQo2IzkpxXqmU4zdb_vcHQ8IbIj3_7w0RyrGKlKExGNy-_qtBtwjojKpm5oHnur1OzvdozR-Wru3bVzsx17F6TMl1zbge9rOmIswEbVC2LRJ9eak6BGTu4sG703gkWWlb6W1gC9Dk-4gQnmn4gSSO-kpd_dGNUt06T_37IAWHE7_zpVzV9XaxsQEAL1uQX9-BRbfX9NakPUwobWOdWrfwyPkyEungjD4hgxEhMWvVlJxqNS1H2fqeYkPLACA&prev=RQD0531E8188BDFB&p=8&pg=68)

* Italy
* IQVIA
* La Spezia
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/598299aef4162d8d?ql=l&sig=64b6be31ab4deac1112ccee2be70ee586ee339dd&e=9uQoF33uTpWJyTo8zdZ8ARLeDnCzVH_Get-TWM1Od1esa2STlZOmh6lyLM_oVkt8QoT3CuMSKDFj8BMbZwyC5Cnk3nNixYu37Vf_0DQ91A7o_guYRXybBpDev74OxWDNRJ5FrerZ-uWNBVmHvLIU92RfoHnJqgbKgYAFP4gWMkz5MU_EBpk6Jbu-r6576iePrRATWG53LjIYdqfMuPIw9uufbJF0VG_N6YO_pt-SH_wETuhoOkHoaeUzbuec--vBv8u0TubCJ4_xEnkojBK1aryE2652H0pI_O_z55uE2d_fySJypJ22clsmCgog6WfOVceQHs9LWnwS2XX8rTtC77om9btJmf_HBhyT7S-UjAOd9jBjHtpOEHBd3AChWM7QAoJPYn-YAmPbtqixBeheo_Q5XO4UFxMuTViP7Z8oTG9FA4LeNPgG2e6wtruMNMMqyoG0OR_vBHFBHmiploTXDNsAICj7kxr1srtwHbtnfbIVxeL-HSnoqNklW8CV9whO6bzbIrDRf1EaA_Tsiy6McV4GeUL05UGtbYZpmjzvBpOLPjLWcKiRDILEY6fStB7ow_twxQdMhA_noF7D-FsTGZyMZSh-M0o2U5rlHe23Czy-wIAraw4KJQJRfM4-kpCDdpMZWXf95Fm_59o0i8x0cV122bKSlOcWLkAFdpYJfLbKRGSg7cuOpTqxWvaItlOh-IgQLRsmVkaJ9QXbDLvXYf8xDbCGcwUDwGXiPsEUXbKW9U_TXjOgH9Qk_T9plbaeB6DOvqzNMRpQAcAzYRr_Ty6xxPIq_FNWITYlAQ137UbYHMeHlEEPfGDA9di7eeO-EqYvi8QXPQlgFcgo3gwuK70_lfDwgyAB7SyqFEU-5FRVw3pzyRRpKUpuwXLXPi8q5xppYNLBusCezcIiSfpvKB2FkIAS6azU2jBY2WFYtB9DO1JQeypFso783S6ik4yJ9dLTijFayukx6ryo51EYY0ZM0H30x3gGuF-IsYyk3Zy6A0jW4gQFaUqMtzu_hUrgLMq8CsodgsHcSZGEoGsGwxYXDGh6mlWiTiYUJ1sZLZCiMni47gBypIVmI52ggRdAdsnA0d63hHL_RzzF48IG1yJAvcT59ynCJevWS3ShGUtnwxIQEBpyanx2uQEMs4v44Wn7DPZD7trT0erta0B7CfGkGUu38gdBlWTqiT_eAr4l9yPV5CodZRbD4EOp5KZ0yje3eSSVp6JPbWn7P9MJGfw7jpF6G2Oq2V9h5FAL6dxAbQwmggHjZ9-36kXRVtEg46NS17ytZzOjyxhuhGHJTM30DcNGPD9lWy_77LvV00EyKgSBikT7HOpKkJjErsRAjSNHsfsGFtgPhXsimrvE7nBoUYmL0Vw8HH6a5LQw0HQtXIf7dfIe8h6bGA7iAp4LcUpkA43KvFtRb40hGMUeSVjYHTapBgb5HMJCnAQBcUJslvUHO_Tx8mP3q7CQsL-eNrdBSNcmv2TXuJgIkI2QvR8&prev=RQD0531E8188BDFB&p=9&pg=68)

* Italy
* IQVIA
* Belluno
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/f56ae339df704ef7?ql=l&sig=b5081d1d42bc452be9935a41632be688b64d0004&e=-fF5nwhy9nJPUD7poZM3JLQ6kAqHKEhUj6q5fxWIWPgPzsnbZLz5i4Nz9Re1ddYrq4hQXnub3vT2sVF-Qw_zVxWdsen2E44GCgsEA_UhFfMp6OCKByidMHDHi-6YOz72D3aIAP8Iv5yy71Vo7MGion-KY1exvY4S3VnDe3g9mk_iSukz-D8K3LClsj2OGx6zpmbzB11MRH89ZxYlbZuZS4OvSQ8gXQowti_G5Otw4u_58wS-zvyLZ0hYqKbdCftO92VqLCRO9pRfqks7Dm7LW2FCIOXtL5uaWBKugMVmhIz3XPxl2U-8ZcWj20f1Kgx2dzNvQJ5F9UeeaprVj1e1czGFfwczDxVnOHfIhzPi4xFsdPhMHZofOaSZm0ae5gPEtQvN5DAuzI0YA0km7Jur8NIGxvzCDEkk3Bnwb_yPHbekX28tOJz5HRcekl-E672u2FLzk1FLOKr1Z7l1mkC2hl88krtKUjVcgfLCiwFx-qxKrwX4cWL_IdMuN3hCEZvqgU9fLt-PCGL9vdVn24DSE7xQHhyuUhzza2oNtqzwdwYNG8_Msr3GbXolktDF845HOKrlzOAmJacgZ1QG_ArsIxGzDdrIIKn9PeCLJZxuTCgHL_LrvluNRltJdhrEOB1LIzPL3o22RH0yqoeilEBkojoG6zKfOSU1nCgeJ-dviDgKIT7mYAiHiEgJy6TRBjmcFAzGHG-hdrFaff9mQmZYTgTlr5enB11Ucit9G0MPRoWsDFN8J3y3FZsEBiS5WGpgkpqbAsH0VqVPROGGd-cL6OibfZickqk5qR590MUgof8gCrsNPqHVNkL9Or1EsGw7dqnxplRGGtNAgn_BuA6zdV32hSaWjp1fmAaqqNA_l8nHtLlrQNLfJIBXMGIa8XqBObV2TQ38nE3VMWb-kWzbl4Hnn2PORwhbZzOPaGHyYzTLClZ4d6XMomYyrWDZPcMrmbk9gy-wbxhVraya2E1MfccwvhdoCIN5gHjfWWUMFLljOni2YkML-lmLmBEFyUZo-08rD3r9biPZEhGQhfnDNQDTWAe5yshccnjOJoKjI1LlZICkR_fcBz1HguGY20HNkjUJWdf6JBZ_CUcmHN4MJ6J5QEccl_qDwOIPFO14DI5h_MhKMYcfXm_eG3XSJV4Wl44cPEVu1opEzeDwwJrwgjm1Maa_l34v5yBfU-hBr4NYeLNxivrvGEvlwI5y6Siy-susl53swLKNoKEykiHhcqgT_uFoDS-Ef4zcS5P_OHhIfUPUt5OvT6ORkK3YZcsBpkowKYSD0YhpQKwm9x0zvbNVjm3j8aVYIfNDw7PfpGZv4F8GCjlCBqujy5H5WTvbpko9amR8-bIAy-EEMK-Dzg_y91kI4ql1CiGB4t5N-BdumMzYwbHMWqNCu5gYvo_fZTmoGn30nbSpNtizln4MIO3gfwQ1OB6gE8kGmSFVoD27FfvAw8rSov1Mau62M6QdCOw4crSCWXBDrq5b3KNo6g&prev=RQD0531E8188BDFB&p=10&pg=68)

* Italy
* IQVIA
* Lecce
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/789c7ddbd1f78754?ql=l&sig=e86d03c248f3a11ab30f2d90721db1bf29ce4e77&e=pD4tHgmIu7iXwFxTOko0iCTS6lN_SjejICiumGjQtfDEPbrXD2hDi2GBn-2TlMwwRhfAdt37QPMBJQd9fjTfLSGieROij_DwQwuBfVKuSyBGnmcfPbd4LYFFElJNKforbchJPWuJ0jWWItegpTPoCvwondbj7_3VQG38kXKlMKyoj3CDPJf9yHZSOoCJNX9fLgUePX2WNZQh7yU98wMaeEcpuiHAseOLwE7JUyYXwexkGrhLTHpDZTlQ2NMehK02b6AJHx2-xMyY08LmBMHbiw5bnkPkaZmA3yjkIBKCvA_qBgHgqj6-5e9CmhRpuvXLTXvzd7Hd07M6mIICv7Iwo4VdYuFIvlhBROB7Kc2Ze_KQRCq1qG06GDQlaDP_5h7lBNVxHgM7RAzZAMZvQD_MMp04yKz5sz74RsAnm5Y1MOB8IpNZV0m98X17lutfkrspAk-SOCEgxGwhwYgfs7y_eXX0Z0WtrVFyBpH59gzt2p4BKTK1Br95LXwkdbhE4hhgqyUjCLJMmj7_X43R-ZOI8ll95nBQD7jZwXDGWJNYUDP2IjCAqQ-ApGuDR2B10XWUfrc0nc3ItATKE78B-KvXD113cRd18jlLHBPoGCQo_GX9U6b5LZKR2ha3zsaaYE3UhsLtCjnXE4FcKPUqTjhfpF6kxf7iHhtPNIKKylgkKhc6z0KmysIB7hEeMuDX5eoPvdlDHQK9zn-L0ewNJSTD81yD32YjYMnWCxTIw9-3Dg2MuDuoXNsWGRzIVOKfQNTDuP-S1QpvWa1O4B1Bf3IzB4rg_QY0afXhTh0AjdWqikjaBZwgh3mNKVL__ssLWknqax-0wSt47UxqZzkKrzyPP7mh7hydg6S9yx7-c2e1RxRISP6UqMWDNS7_vxqh2gbCvyh9zubvXx2RQ1M1IhbcEcP6JX0cHdShX92QUOT-fkAeBUbgKPxzAm3t8gGBsZ73Z9F9lOl8hwSt-bnPnutptFTJgXVp4-3Dn4hvuUvt-7DNkUPNPrvqw3xEygz1eutpOWhWluc38vbh89hSZkz-XQkGVQxhu_-bPSJdvxdzCJe9urkfkLk9DHWHH1pYVDobHPB1cPoUrhqgtAm5AetC9vsLJxUo_RbzGNAIlhQ3M1AjpV9FyxDqxuSCghtFG4V8wTkpxwsUrnVEH8AEGzAWWDq2RSGq1sn4h02EXIr19TPWR4sL3cTaVVOG7U845kZrzBiJe92kFIiJzC9XdEWGA7B1-6KxU_hSCuOMUZOLJ6FXtWAcu46z_DU4Zmq8T4JLe1pnuOrIH3WyR9CUBYmYMaXSaAr3VDI4plzFsOYP4RUYbAYmSlSSr7x7d_GaVdlRhzvmoCKAE4XIIatr82RukISPAquVwoY8-lmk9HexUBXPpZ2hXoI4Agd3LlI8M3aPPVq8-rPTjjh0OErqUvDjjCyYjfbyC27Bxn6p5FDXLLlsBo00cyOzlrDsUVT3hVJDj-0xuO0Bk_KXMFrNNf73p2I&prev=RQD0531E8188BDFB&p=11&pg=68)

* Italy
* IQVIA
* Latina
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/2bc7a2482fa789b1?ql=l&sig=944c9ba9610d75e2dc794afdb2667934aa54bda8&e=6ifvEYef_VI0cLyve7kYUKNCY0habqhivxISkCqmaJajg2gywIAm2XF3P7UiAPW4GqN_mL0HEZCazsrOGlMaj4znQ34p6TIpaH9qqO6bCvEzk97fAUn1muEgCnT-ETsRawdBSJXV-YxuTrKWYxZl9gBd80BbbAGMYSCacSBGpKp_9m4LAZORnwMOoYT5P9bHyydQWVUgOA2xc_NCBmBNVNua7FG4C9jn5e7mskEnmKds-Q2trRrGwPSiAy8WaN8sVKKeNqrWogBDJUgkXJrdVicaemyo8zyieWsRifb6SqQH1P-dZqepfAOnJiZccXrX9HDFSsrwWiz4rn27ZVoQAEMKaREIWeAT1ghTXYX6ez3tsCjAKtaVRX83p2FxqwYKyVkWsiNcfEL0nVWQc-r9rHMysvTMfT0eEhuuRWfLaY_uVBNg41uKjSKXUNAMGQOu2OnCQa2SlPELU12t-YZGUbrMw-rBBt3xoFUGZcku8rMaZdHa3njoDznb_sDfpBywSfZkJ9kdf-FwANOI67q2wcWs6xh3MIX2REqBjydezwL-hMkbn38pNe4RMyQnr3Q-SizSE2SzM3CC9Q7DKSep66jLP-0kQYFKix8ygqf0ehNA9aUL83QRAya6ivAhnV8f4RmNEZL8nmAT9Yfd67Qs8oOyjsZHDLLdE872-nvBT99Ig1jLcpW_ghoV_R4oll8OPnzBQWM9LCzZrGC0vtaoImFKFXvBQ4Vl9Tf1_t9-k2LS8DmKbrwFKbIk6C0jhhSur9e7v5gm6PEsSxJKqGtD_O-g6hC0bXum3y6QHLyZpRCKZfUwD4lxbRg6kzbzCxIHWC6uZo0anaXQPH6_Sesd8Pr9N5UUSN4C9TvW0f3KT-LE7yrMvhPumNY3ordCd_0BYLqHwng0z_cF6vE1VBFhL2OpJBgRcgJ-FvBBuVDd4jLpjIlnuPy3xXBxQxrehVGRnFHryXyhlh-W6KwcXekRcFcQVWsUUdrxK2CtlinuEddKp3p94H-CAwN1O-KAApvl4RhyutDjqKdTykk3cJQgZKYwG37p2mXlXbLXLjcgG2-0rceCnArKsQ6jPfHT3F-ejfSKZSsIr4SLCcITa-qcqXQ7td3F3lrc4D-YEUl29zqUnf6VkZ0_YCb21qjuTfCrgyJE53lRASXgMOXnNJoFro5LvltAz5Yg20orZ-R_zVwFNQM-gkKaL5VQ5QURhkc57WNZLri5f7d-JVwdr1LJq3yP9QZ-Zc0wdB89NJI-9E6Oq_bLclfHAEfHTB8447VIUvHkvByEuHjvJWks8pkHTcR8G_8nX7l4f_6Q9UsNIv0_hMMZ6gcgasVNPXPtms4bNPx03wB4yQ7dYifZczDL4HzxvSX_s1sCcvC_9RUCEa0KfvKr2ogSQc5V16bGK_4rYsquclBubE3fHLRtLnekLWfrQ-UUe3dCmTswN4yeDJGMeeayvz02GQmmnm0hxgS8OfGJfKQDdReV0Dh05cTRsA&prev=RQD0531E8188BDFB&p=12&pg=68)

* Italy
* IQVIA
* Lecco
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/8d044916cf721670?ql=l&sig=1c3b9ab9226d8ba52abcebc56912601e6c193c41&e=QuPD1CPDG2JhE7EUf5G_AL7GLrREdMHJOolTP6zJ0HlsN6J_fTWPD1nrPwcMCX_3SYKtp5aY2omTSDjLD4aQdOGKT-TkVzmQTpoa1HDweOmFUVXc-XKE7mnaYpqUYi5g4xAUpmj5aM-aGnRlbeV7WXB0_Qbdhp2SBlnpenu63N8E0bdN2iEFGuARwF67sROtg4YNU-o70Nmxg3skQMp9E65Li4FPGokWbCBAuNrxfKtbGAfqVQW3tN1TOMHRDJp7xYt7uGg_DKjBwQV4_msJJTXxvgKXTXBBzxDVp2jP6187OtpZIOGxsqXx1hbvbSDR9fM7OFGGQGH5sV_vnEVEqaUHMoWbo_rLEh48byFnweSCDTSmQfG5pUWUv--2bl0Zj8AtyC7FgTf04bYOrwx9umSxSNO9iXn5o2dP8fcEBpHRYNbbvcqEncCszZVbvxMo46G5pLNr7XGYhM1xYu73Wp2G6oPdAsb6zUVyn3KQXFIHC-7yfJ1d3NxtlEb4ORVg5DpWIvj0bCfk3YlT4UFly8Hu-OWktsupQNLUj_407CyYi6weUzMddPfGBT-gkrwYi0mhBjNUUHqIvZ8uX-R6IDiUUkqUV_P823NjHcYfTc8n95G1vJyrUXxY4UcmOCe-TsB4UeUGXcd7dqmdHazEjsdmjUaH_rTsWAycfNj-Wz51B39ng-I5w4rjVIgGUf2WtqwMUTyZX8COM3OZHwDgbyc-3I5TboLqnlGW3LwbpOsA84b5COw8NxcuDpeaqx-kOVqAt6PejQ5QtAoO7fddoHqa0nekil7iME9AvMPGyiyA4AYyk5VNA4Og0e4hmM4O4Q-dvAuJz4Hs13ZF9dy6256K-sC5thSDP911To2ugbTCsfZ6evyYySQVq5h6kZWTeKq-Lfj_8SkV73TagiRXmPCd9clD0WNprp56aOHySEHP9183qWeIuie-caJYhT3wbzg4d6ytLcpPF1xMRCI4P1rxLuCKYHK4tCO_fSPsw39qHKJfYCM7NbIxDSmJ_1nZW_0Y4ITb_KBPRCIQAHwAtaN6sGaF31B3-RT96EmYoLabirAu5nnR6N0kBM01Ebz4kQ8IhsQarophOm_BUIx4ArSb1AtQ5dQz0u3aCg1ipvCI9KXe5zMKSPzgO7hPfkcl0yOkryYmXX7YcSMu93vFiLBVBAuhSFfMds0UwayjZsjAiAke0-T6hnYxF9My1j3zUk6SOScqRhhrX30CREU4G5sZvwg3Okq1qZzBZNgEW5ZrH4DNsgec9Q-jZ8aBK07A8x4FMs-OBCMnZdydJxBOHrYZMT9e0_dnbbgdFmENietnrrRRQpM5BTebzEqVGwtQ5TEKFzij537saR5eH1ytFWx0krnx4wxbiLmWUj7KJtqgtF_0rMzhbkMZ5SkK6AzJYNgfzTMAu5GPzsIDSbXHxIFIAdphEOqvNpnhppFFrDrIhL4kesokVZAZI0pXxMrQpnBj8a8UNoWOisvsUr-PiiU&prev=RQD0531E8188BDFB&p=13&pg=68)

* Italy
* IQVIA
* Rovigo
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/5d65240d374d44cd?ql=l&sig=0041b8273de48ce8305e60396a854e4bcf607dd6&e=8UNhVtV7ZZSQyAY8n_Zh3fJHBbcRGe2WKyXMD5TyJmbrHWkuslWYdbP5HabYbQY0CuM_3IHYeVze-o4dSgwfsLxQ-k2I5YMeADWId0kWyGGlpuWYDuYml0zK_43KKxYFfa9b_IDe8biIkL1xN-NquDChZ3P0O4om1RCmzt8nw5mX69gdKCKrhCRi5beAulngw9ZZcdwRoH7D1T9e6WXQAkgxAJtPAJuUFYxJv8DYTzZj6WewWPL_v-qDDvJAHHGRNdw4e8htRzEp0taEUPb6I1lhhaIakhpUc4ySKMdHY3Lha1DZqQzzXs9sNP5lFUpcK67GKlgHPnpz182f-_t8tKNNfR3xSDwjMHiSmQ5aV8eASr8DeJUb2rHk1R-ieYut3h4QtCOZHpPcCO31nNouSrZolSI1q3Z6ZP6eaF-lNXIFYfszb_38o-4x0ehAOJ-3vq64D60Y-lgcBY5VhQgZKjkZmW6jfd5yWStpnu2zGdt3rYMJByANjzI_XS67jsCrLCmDlT7Eq-5Bh4AKwO6NJtRScoVkNMAek89OR0JhbYN1Da4nYgAQ5x4hyDbZbUp6NLfO4f90qPk5uy9NdvJgNcgtQOqdW2uI5e5MKnhbgt9u9lMFj4aUOw2huOIfV1RSYVNKqOIDdXVbLoTimIeExwIQj9Y1ou6k3hZQAtaC8y_J-AAjpEystaAKDxbcw-0HOa_oukW94aJZnp853q65afdi8YIRNQJNRZ2ibTjkRDao6crOHz6q67TkvlC7jz0vbLx9YzDNlV_Z4Te7Io-VnpXvP4qqvsB7-XQ2Emx8tlQW0EyfIFKEbhPECU4jI07t9LI8qZEl-CvGIAdp8ZU8FO60-oMmlJctUiXjSHQlecJs5m_8jhX1O9tJvlQH2hn1G38yX7yuPwVLzn_UrOlOt9mZcJJLE1_fT1ipXyvbXsIW73gkJUdSwjGi6QKjrBGik2s9DvhRCK0dFiOxa4Mz02mv58QZhSvCwnKr9GUxSRziainHZN-IqV9rw0kPtfw_OAysl6Pzs9LYFas5EcCOnOBuXrQIQGvC_HuP9jT5Bt6qZKlMsEzMJix5L-ORdg0rjPAbbJd4WJNUdRHkB9mI75nvvgeKLf5e3pjNZwYibxMDWM1p-DkoGwFzh541JobjDKbVKRoPhhCg00v4Y59kHu3bn-lzCNb8PH_SJzUhEhFaMHKye1XBucSrir1NKWJIXc1Jxb8RmCvzzVv4P2ipmc8TDPMnodTfI9mG1PwFajGuxT6ZfAjTczxxk23uJX8yj2hhM_JacabOf6hiu2xVJHwbejgmDWWDjIQMzqRwfhhbBrYSQm3j4fekkToGdx1xz_ShQKfWI7RDWYS4JbKQgNK5K_UKG8asvlGZGX5WPRtbn2bc6nUnL3jHJ0jEcCAngHFmJGqtpAEdwvAM4cr1KqLCR0_vIChtHFoHy9ZwBv8NNqO9BcT-IUFjGHpjpJBu21uaOclYAuvZU-I4tZG-&prev=RQD0531E8188BDFB&p=14&pg=68)

* Italy
* IQVIA
* Asti
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/a09eb81db7b5568c?ql=l&sig=7102019ee69126c0c043c8b6846bc47aa0504a4f&e=wemSfCowVoUc5Lbx__JgLptEfuIkVAVLhHBnjCMgP535NiEsWGBx1EAzt9A-60QUVDKgDqisdRZ5oB4gvDcmHopfH6wzbNK_7GBdEDGvNpFWKpYWl_ITMig0cug6-MR8JuAYEZu9tMc9_PYrYu0aU4HUYD9FLCGHWD6NMoMXfDA0g2ajKHqWhizTpXqAWiYYMGACHJfwrB7Q4JXyQfvuRI_OMKPCWVcrzF9g9v_nD-DmDvGWJQYt7AR0SVwX7H---aFz-lKvoVksl4xsc0obqiffelP2e_g2U92KI7eDLCV6PGMjOFSm4YTta-HF7jRAPzZfcbNWGdDG05aVw9sBM-7ts0ZyXduj1_Vi3tmMfwBddpwev6yiXZ4xdZKMWYuOkwreFMhsYxJoV-oxf0Pk4GuHGT9SlAAgplvne8xkEjGRV9zEEv-hH4jautaqy5W_hLY3x7C0GChmZFBBWuJfgEZdSyYyEzy-Pwbanzb758esrArvbJg_JGftYZf1neqy7PlfeSpgnjPTrUluX9C_rxZb3HKvEfU2U1tEULtmFzIDz97tDo2TTh7UcDVJNbT1r4ZuCNvN1IqJuBsofM8zH0LUlw7SJ72qHUBBmMAwSRoYhmuugNteGTHq0pcaGfhnaFg0MdjhmEz9fJySShyg2JJJuu1s7Td0mmjfD0bCJx9v2uh5E84yn18ePaKgnBYeHqcqkb_xRPdjESvY753vhya1oB0KFVhzIup1yYkIu4b7lf2hh2PxyuKXpwGMdE3Br_dls_s_BcAxVOrb9iWqMFtmmGdqPlcRN7IuB2mogO_bqU3zltm0sqUXZvl6ZT4IOecihDA0RxdN1fAnl3TDuZZ6L4DElCnuUqBV7umD3FIJrDFwUqabRkQN_E8VDeio7cWVr4dNxLORaujYKgXSsynczouDjUzGrfS3zkgO-LKI1UYjbQ4aXQsXwv_7zfE7gmscjAnf3gu1O4BZwYoK2skeSoxUZwBkzWoYwGyoq5rJdMM13U65kFESG8EWoTTh_dF7ZMYNZ0AaMt7obXQLCy40YgsQB-jPoWpvU0pjyrJ9qmFMw25iFpa_ApVGH1YORr3KzahEv6UQBUa7NqmpCAvieqxWm0h4rxjtmizUyDUrPg1tX_F7pFP23PDe8HtXORMux8_tfpl-YNrgMsLrww1mRPvHac24BML8k0V2VEIq635WQhYNdMHLVpdOIVolBpOXXs-nwKVPZ4Re1lMHbchpXOhaa2R7nlNkVc_SMWP15erIkE7TiLt7oStC1xfVobdKQaPqWiaEL7y_n5Zmg1ZQOyejPYZx1KBXFDvHBbMMDe-ooEmQkFyBa-VV4sPZzGbSxEKf6tzWUAYZfBc96o7RX4c6Up2UfGpIVIqlGa1qkR-MqNuxusCEqWNZZIDNzpdUQ6w-8O6nWlQt3coXZWTn6sEmkAJLYw9ty7G0vLM46xp8-g9Eyc6_Ia_B1zxT11-cRj_ecPOZ87fos7W6N24&prev=RQD0531E8188BDFB&p=15&pg=68)

* Italy
* IQVIA
* Biella
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/29481487310edbe2?ql=l&sig=675f696c95fd37a00f1e0d6c099bdd91d94b08df&e=fmv1A9ZZfe18hXQqNPJ0yeBiEE--8fL4xSrIQwUYh_P6fdkS181KMunizg7gxSSmu24yQTBmEIN812pGFc5wnV42g7-taxrTellZWsJ7rw8yfcovX4pRr51YzRIboiDg0l2E9FRy-y_--NhozMQpuhfNwnDCa0KCgTY1hpzbeC4eN9ta80pdLOK5f22T-VvJXJGBxDQ6eYMl11mzmSQKmlczQ7_DehSzVNyKy8Y9p-DT17jc66IBqZGzYKX6dmmdu-6SQ-rUFcNRv1bP-2RSnJenmqkxcKLvJP7lGNAiE9DRG6EAIoTtpeWhergd1XAh5zZ7Nq6hIBk8S4HkXYHZBej3TpdWZ7o38pu5Fx8KchTluXHGSHnpPSS-Pg5RcURtBNI51DVV-7_mlw4SfKPX4J6_SI87Ob7uuzfFbxbg2PijoN1KNDrQUUEwirErHsB3QfV7jHZhMeTodUDopgBzdnkXxhIx7_qkPy02ZAix2lTVqYvhbl4-BYopoNsl9gFUC4wjQWcRJ4Z32NXqm73c4mLjct6lHCynOQkD8nXQ6zb5A5vsYV59__NMFho1uO0ayof7w6dcfZiDevowEBonYCCjMzG8VbRUJmkYFwwFy0jboDAhZSpmOURZPfTA5xHgTcAGMFruDJ_05QEEDgLxGlBAybuFG6KPgAtfGCiOKGpDyPHOjocevviaztDy-pQoL6-YzhYu9Yq9Z47uBu62s5eHJw3uMHKCyHhMQit63gLUQEI3GKjWRH8UulnF3SGr-JcgB3tdtJfsLxPmvmIFSOD-fnSRIgGqlfSGv3L_oyBesNgauGfHMFmDg7AxrWMcIHBUbuAbcx_U2yCfu_DNT0UmED9cmmUTA9SBm-r39jgDIFR78TMIkNx_wMcGRspfWYvivZten90bHGu7sQ00KYAUIGuxZvS8jqmR00CFDG8erpvBnm0J3i78BBmug4oe8e5SZpocjOnw3uALuYdU-6zmQ2kosNRIbU3RG9RzaGUZ1FK53E40kSGYgkjPG93E3IARUwiS_J_jGR2YhhQ3fLqTeJuj6gkfAffsjIvP7o-fAjXSiKirw9WL4HgKyP6kBo3sQcOSSqomG5M-ETeuK8yu_KoOqbX_drZSleXdcxP8X0YP9ihT1NdlwB-tVGcmSKsXxyQoHoKfbI8zo6CXR168z5JC8hfSO4Zyf6oBFEAEMrbp8yDowI3ClsSZcKBwUvMoZsymsogfOwGJC8YCMkGE86aVpR75-zJ-SnVRDopX97yuYTNFVPBIQlo3i4tan_5M6qFmF1nmAJbZGRfQsXz1SE10u44UzowskF8KLm0lW4ggyahid0SObd6BCW_884x8-UpVW02kSSDnD5COM7iqHEYUVJV0kTx9SEfW845cm_pL4yVOZa3yni0cHlxtsvpJpP9b5tRWUAIokdOwfsTCZDQ3P5Rtmg3AuAQTG6XSs4HDShZUQ40l1h4yAM9E8s0Ekz8Uhr3kCM5sBM_aFo1uxlvx69tDHO78zxkV&prev=RQD0531E8188BDFB&p=16&pg=68)

* Italy
* IQVIA
* Trentino-Alto Adige
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/b9427b457d646fbb?ql=l&sig=453e6f37c405471a48489407e35d6e2f3b8d4841&e=0pTgje6quTls9ky5cC6Y8ZpB9lTlELgIGQvI8wISYxEPY_k616uvkLV4pXW8cn0Zns6J-rt0UThQ9cMGO5V5SmDHv1TCO3FdEUQy2vo7d5NPxaYAlOgu0w6kuxTTt9ThxrYA-plXERtl4cIoGonw3mMJ9PH9SqB3gkl_zwuya06UhOWmL9uFOKQN1uw28ZG14pbe9UatGO9GVCLYREX4ib2LuEPT6tH4F0u-gslLcJtvqpwZ6ubwEHoo10O0x7ovZis8W8DFsbTT0M2QvAE6iIB-qUxshxyGwAVQSUKfEBGBq59kjgXECCY5eBafe3K3pLklpNJEQ0uJ7DPeNXMI3-jd_MLELHLqM3eK5E0anGDJDkNO5HyC2hJDolhYBWjOdqsElIo9GauU1qaj2BM78kagzMsZ2pqtJ_y5M45aKPB12HiJ2t7e_mrpB5oylTItlzuSeX0Hiyw1rPhtqIhBaWhXIkAxfZHJMgAsvltRacpVnOvC0ZWhNaKRI5AnTatCA4sWz2haTsaH1BIxKHPdy3LMCcZNPaNnxhoZ7ckJSjXql9ORCHpPhrcTammELhfuvsJ891MhmUaVYaV9WWQiJ5cNF7KfafjzGBj-W7BVndbNqFEGtoo4fOJVYvnbgXZizbnlmoPwOHQXGKb-GLq3gOEagCSxKPEKx_TX4Is_zpVxCw5W1CojxE7U9LlXu3dC7ariWDHOMqKGlUtzq3spu7M-1bZpQFDvyHytlQSkhSt5qG9n3YzOCbb78jYMR-TT5HebUwBQMi7FHhmX_-17CgSi-_skmFU3xbNarJ_S0CtvdCymy9MhdqxVeeF9bCUH2B-9e-Lg6jelJCt76wUBheUpMZR2VF-HAkk4k54CanK20KZYERDH45d7ECRTA9A85mHK90zN2bPKt3zygA1FNvmGbF2R-QPzxp_3mRF9tjMu_EMqcre3sO2JSNBoPmvKfd-oMMYj1RVMQh77CclWR44m2rvEfgiQZMAiAWQFyuIDERbViYEG6VW0LuTrSaPHt26PZ1TjHgIwT5CwLuI7fP-I9H3bn1RqRSE6qgYX6c0UARhWhbTIHLbRY5e3rD9apQlGMcaYoyGvU-M9Quiot_cAavBz1WRqFo-G70lSjUlEZaOYfmoVkKpbRdsyUvUQt69wCDAE0ooMhroW8WFZdbSaRxYWIAnEuZxp4PkCWcf-vAhpSI5XW_fbJ86x6hsn3f3o9R1oS1WxHi3suMOS0hTJgo544Tyq1bbhIoq7GvcIrm97P8EpbvqJTySq5ceEM7XwpQZtlLkYlLp_u6rc2cXbIgx1UgQ3XGE91jXi7rc4aBPHC2uRb_en4rsoSM1vBAx47amzsbLwS8r1tdGFV3eq36Qrl9MKjmiQxGPuKQ-UqivjsMYWwTnXtc5hVNU3ToyTmk9k_P10JINFZHV-SyEpRMQvxpicxRE4_WO4EXFMdj7YQXpVQUOVPUpzQ1cZHtq1E4ClcH4NIgh19cFrwQ&prev=RQD0531E8188BDFB&p=17&pg=68)

* Italy
* IQVIA
* Siena
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/2c747f46ba900a38?ql=l&sig=f745ff53ecf5bf9a5734dd7755596f8236819374&e=OaR2pIFL967KH_GYg54IAaC9sMmCjk8gr_c8CLzpm3HPUZT8SU7poNNby8DdBHI-HyHDfhsf6effs1H8RVIfJLGlshD8-XQJOQK0c9uxPADoBCpkicPwOa040ZGBx7Jz9-nzp0S54Oz8XERgtJC7ScvL-S0BeZhhuhvLgMKfpVYZFeTX3sS-sPIjT40O5vOY6HI1Br3PQdxuM_iBWqoX8DjkFbPVpZ3-CzxtxM7oRFRSDC6sbQyZKtOdRybwwiwekiVYy9S1ssnRjinAoWOQkLwtdhwS3crGQRvockWYWBH2gIjs5qS121ccmNcOP2gp3SHuTXhkntnkuYgD7INc5ipcnWg1y8cguh6MoAgPDXwDADKRTVHsL9-X1jlYVx_BCsQCqmU6bDJ5tNVCk6HCzo0vC_AK7zXipyMuoixFc2yx9BQGadXGqR-IsV6k-0JCgfr6NZ4LnGMSYMHFdWvQvUKeNtonwgF0pudKHO2cIeYwdSSBmn_n0p7-biviOzm4c2Yh4kXxuyhNLllwz8I3WahyZdfBGjHY7vxXFeNXzUlmK2ywj2MChPea5DjYu7s9dKzk-AQy-w5oyLMn2wiLBIP5ssMqO2WGwuNKQ5GRT0vTwDaSm6UIDuTQ-WUz92HhgX64JJrnltphaIDVBWqpEwbtom1GNSdds0XXKDjVfW7kcopB_lV83Y1rPtygDlSjHot-RDp6IQD43Tr-RMnYvHWtxNAxZhXa9UR3K3fGP2sc_vqpaw7ciViO6RAznVmeap6B6PERKST9kMEIawlPkLt9n22aIuztyJIk5H3WtlauamT8GMwqMTV_XObP8wwnc_Ab1lhqHrNo885Evo65N6bINUVQNqv28Y3jdrXnrXuDBmrK8_zofP9znmXj_O7IY8htrvb2sUkCM9CQGLmXj4WK7GCoYu9-BFnzPZ1KsyYQNITJ0rbo5rIz-Uq6j_agws-DVAeHdeNrXlm0piBl7cvVe2xcdbJCoxiTXVkHIRxv1kUAQkWVI3hyl-iLhPgTTb0Rpg7Ppp7ABcrwUZAjwhXz4dSOL9z91MVcqg4DDud0k8TTnM3hTfSttKmdWADzOeV-wl68gDxbCnmeFIl0ce5sIBqn1L7Chhhr3xuG2t6MC46Pw4FnPBDA_fnQziSX-mIVVF4rOJ5zdV0uaoq_ozGbBAMJbPtB517zNb5R_OznOsPhu6pwneS9GOV-rxP_AMwz0uzklkQcluJp3JmYrQGKY7JDAUrErdDAdZ8nE8FUtQPjuTzDlrkzDMF1cUvDiX-jjDxvq6b8R4NabBSaUPlx3e0CR5_nx265B4PrmwwnYXmWuygyZPkBhvGCKCstR0JMlxrK6ONkOzZy5aQqwZJce4YIute1tAtR6arpXvA6AczaXx_T5GbF3b6ly_4h_X3-iraJCHz8eVwIR7d0VQcjgzsS31jzT8-0BOvYp5pOXeK9_5rrWpUi1dnRQkauDIcYZfikH3l8JH-UsGRAifMO&prev=RQD0531E8188BDFB&p=18&pg=68)

* Italy
* IQVIA
* Pistoia
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/dc76c206520f750a?ql=l&sig=beddee981b990364a67f547841a74624eb9c951c&e=XG7ulQtGwcIT5Ac6UFD9o5cT6PmM_VRUunJK70iGFx4RFovQj-3GRHya3TmdwO3NQua5j9fJaHreN6wQDQgzC4BhCoXAUYTzJj-Xo8U9JNb-aqTPxrBlH35SBWdn2kE9DnKkApd70_a2-qpuPg9o_egirfyLF3pKajiu7A6YY6LOEOX0DPd8ESqDfEkqGHJISFx-7wx51JFGSPMxo5Xd6dtw2NdSSrVQJ2Q-ATrmTfmEpKTQ9-N2QpW8umu1j2tAg3SCpsrncbUgNbn3mdSmlc78IW8Fv-vSOiJtFUIgjIc3b1WAw1md-V7FsgVRKdXmv0MBCC0HYYsTxjI41vzFX65SRIrwIu-a01o9beNf4yYGHEr9kn0R3blYzpPcWnovHJGCJ3oS0fjftvtz1CUBTDEGP15g5VhaNU-cl2e_JGCERqwPIiUse6WyChaKm7dOFeNsFfIS_Rz6UwyEoDn3lsCyBRiC_BS2vbFx-7KXdNShuuooGREWOJkKXS5OpBXAADJTjxvqPJw_FKi9vYgOshpaluM9XWXtqOXjgbDWvzINeZkSjQ1atOf1PqQzeGmccPxJ9wskhrz0yMVcKJ0YnZucMHte1c_N7WBEvo5soqlWrHR3qYVdZZUF2S7va3dRrmoP-3vI17UgcpbzbxmKy85hVaNBUNLko6z-aQxB3wcOmE4WxhX8Ipq-Zl7AwNi0d4dst-orygZqaKoVbjtfS8naryk2hubrvwotrZmG4VgCuzVutBwjxyQzq-f55zkLZYP2_DuG7JM6P3klgEkEIbtdB24v14uXzm2aVLjL8BC0mwz7Vyx2770VCgx3pxq7aMSU-0BP5lUPaYnuW0MsRoUgB8OjFNXJjJiSmXbjRvxI8mDbm4etZQaqTbYiorQA-BJfcouQyl-bXFvYZE3K3ui1-Dt07ejM073ED3CSPILnPoJIlVtIEd3wpVIj58qVP2CdWsrkZJIFdGkDuji9XhUnrMikIJbpFa3PRpfoDvn8voEF5kHe8s6UmGHbG6inDXWoBgkJ8PVhu2OuZR5w-GzGEvCQFd9CgbgVvcXOoHKOlfLlhsOKijI8-8x6QQZpThoBg0aLvVYLOCXfFOoN2lLGChp2cbZISU79wcy7aIXFsQbqO7A6yUcZ_8BU8bysmXBTaPzX57bqgveLHnxIPlpVW0WKbLcBC2fU1RGWPMHm846lcJi_WftmKY4NJ3tk2ErJLb6re-DXXPISTMIg_p8cez7GHEPyi0sCz3vipNvHJY_Ix3sg-j8Bab6il5y8lFS0aJbLCDuYFSs31c__UP8vm9f5HRK3Lmr0q0qLwXnHfVdgM8b_Y5cKTtJK7nkZf-neeiMaBWP72VwLYNOHzkrkTYwbTrxiEDERG_FksL16Imx2zem7AV2apiCWkKIbTQ9qZ6gsPt6dJTMuWGkDKWzoy6O5HPoBgfnVjFG1HcHQc5cT5ELS7_c_Ui9sLma3XFUp9fNrQbvXZBDniWkKMBlGunywLu20&prev=RQD0531E8188BDFB&p=19&pg=68)

* Italy
* IQVIA
* Ascoli Piceno
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

[### Clinical Research Associate](/clickout/370a497181f5cc8e?ql=l&sig=8601352e1166a39c65f7ae3b82c6179c78566670&e=0bncZ76UW6xzT18WJMo0wwpVn2YzMNtxhfp19dsNA83dIQbas827b-5Hjbk4edl92dQQ65BMKCnkqL6dOgCquF1sJ9oFWiUBsa5O4Ou1gvw394TiB9o0GskEOBs7UwDmyBNdC4lPkngOO3v6WYVmH3UIZaH55Bfn8HWh7QPpaXBU0K5ve_8zjAKXF0QvpgIf133_g_reaYydD7UmUfme2RawmKlHhk6PQ0aW3rHzUxI4sT5dvIsNIUdnR1rPCBEBJ9xvl_v4WCq-SER7JkK1GrqGgi6_3KfJTWxougWaNANrnU9HknjYJYvnvoW4aM0IGKJS6uRt8j1t8T4U0tFhV_0msISlQxQEWU4QrD0s4T4S7tp9FckY_lp1TvaupHn3dEZSjDfKnMGi3UwSuclhOc3NhQ7d_c50Pf94VtHxu-kQodxwHqxD8iDq89PyL65sDQFrKW5qLKNaZlyUjgvs05bW3yg0ImPatZy3eoyMXYosJ6dvcrFJiDym6kMfU6nnOPVh41NQzGAfRjpTIFjzufjWr7kFREfZ1OzIWS_C1VHo5t1wuboVqw0L_C3O0KlGd7o-iUoziivdLYyou7QLkqvL_2IYEzufqf5vJ0bJtTHXv9TTFygTndPMMPXNgNcTeRDsDm-LlOzNj24Eawde3eBlF3ao3E5WGkgZsQUt5DIRPl8_1jmyqmepdkSalSAEmUJAvfG64KPK7-Qmr0loNZnWYrrRKnd9rGXiPPZEvB6vZSQSTOA_CAtudCWjYolNVVX1rD0zjZWDap8KAyMtF1xmN2FCLLiKtV6UE25YW9wwKNhcc_WifRV7HMuunCB_xyrYPoAFcBh5JCvITbs8xzkNZ72YSou80EHLpV2pXsyzLjF5qdPRzLZ72PqwPzBawMKsN1jRFKXHlqJ1tZwcOAURCeND93tOwPQHRAv3zweVD3W7F4trvgFMi4fKeg156D7DzGEqdvvaBZsV0n2-o0vV0YFFFHTnfLaQECgi2mNyWohS92W0Q0-YFo8heaR1FG8Ys-D-vcxkNUBJiCwANa4BQU_i8eVLsO6uRm-0hFN2jo2uq-7BLfeita3qwO30saqqNTEOvYqCMWUGTJRrU6oDmifQUxWBJ-3TP86pFETQ_OLdJEC5pMkbXklxVQWhvPhmMpcvbotD_gh9eUpMS_-38CqYC2sJizGZELX8ntJlFm3i3i85ccMKQSmO07Qx2fbofqA5IMGw7YwiTEnc95HBOfrb-F2WIcXd3SysHc9bI2Ka7ueozB6Xs5PVBWqehzc4UOljZxK2D67seAoyEcdXRaNFJ6m9q23CLC_W8SrB7TIsK9xHF0MUykkS35XbY20fV8ZRJPqG2WO2EziVZNXPSDAxsL31npv64VbxcFRLGi28Mh4NURlSVOV8Xdn_w7MFmodY5Q4lofEZN5xgKUeNRuEo7UfyiuZpFnW3bDyU40bhFB8BCW8ugrYZjrLRWqz0cHppR8nQk_6HvG0IVzDqQj4&prev=RQD0531E8188BDFB&p=20&pg=68)

* Italy
* IQVIA
* Frosinone
* November 1

Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

report problem

* [«](/in/italy?page=67)
* [65](/in/italy?page=65)
* [66](/in/italy?page=66)
* [67](/in/italy?page=67)
* 68
* [69](/in/italy?page=69)
* [70](/in/italy?page=70)
* [71](/in/italy?page=71)
* [»](/in/italy?page=69)
[next page](/in/italy?page=69)

* [«](/in/italy?page=67)
* [65](/in/italy?page=65)
* [66](/in/italy?page=66)
* [67](/in/italy?page=67)
* 68
* [69](/in/italy?page=69)
* [70](/in/italy?page=70)
* [71](/in/italy?page=71)
* [»](/in/italy?page=69)

### Italy

![Map of Europe with Italy highlighted](/public/img/europe.svg#it "Italy")

#### Jobs by city

* 935

  ![Milan](/public/img/coa/it.milano.png)

  [Milan](https://englishjobs.it/in/milano)
* 453

  ![Rome](/public/img/coa/it.roma.png)

  [Rome](https://englishjobs.it/in/roma)
* 250

  ![Varese](/public/img/coa/it.varese.png)

  [Varese](https://englishjobs.it/in/varese)
* 227

  ![Bologna](/public/img/coa/it.bologna.png)

  [Bologna](https://englishjobs.it/in/bologna)
* 211

  ![Genoa](/public/img/coa/it.genova.png)

  [Genoa](https://englishjobs.it/in/genova)
* 204

  ![Padua](/public/img/coa/it.padova.png)

  [Padua](https://englishjobs.it/in/padova)
* 186

  ![Verona](/public/img/coa/it.verona.png)

  [Verona](https://englishjobs.it/in/verona)
* 126

  ![Turin](/public/img/coa/it.torino.png)

  [Turin](https://englishjobs.it/in/torino)
* 118

  ![Naples](/public/img/coa/it.napoli.png)

  [Naples](https://englishjobs.it/in/napoli)
* 100

  ![Vicenza](/public/img/coa/it.vicenza.png)

  [Vicenza](https://englishjobs.it/in/vicenza)
* 86

  ![Parma](/public/img/coa/it.parma.png)

  [Parma](https://englishjobs.it/in/parma)
* 84

  ![Venice](/public/img/coa/it.venezia.png)

  [Venice](https://englishjobs.it/in/venezia)
* 79

  ![Latina](/public/img/coa/it.latina.png)

  [Latina](https://englishjobs.it/in/latina)
* 69

  ![Reggio nell'Emilia](/public/img/coa/it.reggio-nell-emilia.png)

  [Reggio nell'Emilia](https://englishjobs.it/in/reggio-nell-emilia)
* 62

  ![Modena](/public/img/coa/it.modena.png)

  [Modena](https://englishjobs.it/in/modena)
* 62

  ![Trieste](/public/img/coa/it.trieste.png)

  [Trieste](https://englishjobs.it/in/trieste)
* 61

  ![Monza](/public/img/coa/it.monza.png)

  [Monza](https://englishjobs.it/in/monza)
* 60

  ![Bolzano](/public/img/coa/it.bolzano.png)

  [Bolzano](https://englishjobs.it/in/bolzano)
* 60

  ![Treviso](/public/img/coa/it.treviso.png)

  [Treviso](https://englishjobs.it/in/treviso)
* 58

  ![Florence](/public/img/coa/it.firenze.png)

  [Florence](https://englishjobs.it/in/firenze)
* 57

  ![Salerno](/public/img/coa/it.salerno.png)

  [Salerno](https://englishjobs.it/in/salerno)
* 53

  ![Bergamo](/public/img/coa/it.bergamo.png)

  [Bergamo](https://englishjobs.it/in/bergamo)
* 51

  ![Bari](/public/img/coa/it.bari.png)

  [Bari](https://englishjobs.it/in/bari)
* 48

  ![Pisa](/public/img/coa/it.pisa.png)

  [Pisa](https://englishjobs.it/in/pisa)
* 46

  ![Brescia](/public/img/coa/it.brescia.png)

  [Brescia](https://englishjobs.it/in/brescia)
* 45

  ![Catania](/public/img/coa/it.catania.png)

  [Catania](https://englishjobs.it/in/catania)
* 45

  ![Siena](/public/img/coa/it.siena.png)

  [Siena](https://englishjobs.it/in/siena)
* 44

  ![Perugia](/public/img/coa/it.perugia.png)

  [Perugia](https://englishjobs.it/in/perugia)
* 44

  ![Pescara](/public/img/coa/it.pescara.png)

  [Pescara](https://englishjobs.it/in/pescara)
* 43

  ![Asti](/public/img/coa/it.asti.png)

  [Asti](https://englishjobs.it/in/asti)

#### Jobs in other countries

* 69308[Europe](/)
* 12877[Netherlands](/in/netherlands)
* 8564[Spain](/in/spain)
* 7968[Portugal](/in/portugal)
* 7765[Denmark](/in/denmark)
* 7403[Germany](/in/germany)
* 5269[Poland](/in/poland)
* 4145[France](/in/france)
* 2620[Belgium](/in/belgium)
* 1197[Luxembourg](/in/luxembourg)
* 1151[Austria](/in/austria)
* 464[Sweden](/in/sweden)
* 354[Norway](/in/norway)
* 304[Finland](/in/finland)
* 272[Romania](/in/romania)
* 234[Hungary](/in/hungary)
* 222[Czech Republic](/in/czech-republic)

## Select languages you speak

Save & Close Cancel

COUNTRY SITES

* [Austria](https://englishjobsearch.at)
* [Belgium](https://englishjobs.be)
* [Switzerland](https://englishjobsearch.ch)
* [Czech Republic](https://englishjobs.cz)
* [Germany](https://englishjobs.de)
* [Denmark](https://englishjobs.dk)
* [Spain](https://englishjobs.es)
* [Finland](https://englishjobs.fi)
* [France](https://englishjobs.fr)
* [Hungary](https://englishjobs.hu)
* [Italy](https://englishjobs.it)
* [Luxembourg](https://englishjobs.lu)
* [Netherlands](https://englishjobsearch.nl)
* [Norway](https://englishjobs.no)
* [Poland](https://englishjobs.pl)
* [Portugal](https://englishjobs.pt)
* [Romania](https://englishjobs.ro)
* [Sweden](https://englishjobsearch.se)

ABOUT

* [FAQ](/faq)
* [For Employers](https://englishjobs.com)
* [Terms and Conditions](/terms)
* [Privacy Statement](/privacy)
* [Cookies](/cookies)
* [Legal Notice](/impressum)
* [Sitemap](/sitemap)
* [llms.txt](/llms.txt)

englishjobs.eu

englishjobs.eu is a Europe-wide search engine for English-speaking professionals, with a dedicated job board in each country.