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# 8855 English-speaking jobs in Italy

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[### Clinical Research Associate](/clickout/68c9dd9211fa6900?ql=l&sig=526762f434e4c664df9b8c0dcefa6d5b9b38b1bc&e=FKfLP4KBApJfQHOGWBAo_GZYF7FNcsy1L_NaIgcu1Z2ePuWpalZMo4P1W0MqwkOjLm2wOhhk0b96jzacaz6CXVrEcqPm6qcJDF5-0E0GIo8JiAggRsvbWiktrSbflqKSs4sNLLB0pR1w041zE-YeEPbhbi-4b4jLHm0gvTj810Z-jdLanN4CZC5Df7bLegu4bcLYUcTSfCHOgataTOjrNZiVhNw05lfZryfs37spJQjXrTXdb2GnovEFJhLXA_N_EHZm1aWUmgzbb6_TXy_QD0zqHEywcVtzbqhAVCGlg2qAJV1SbOHywXvxqnO_b3N2REdVWSkMFy11J0mELZPnOB4NZwxLiirS5Hg5voDtPg759AHHPbSJTESmJsItIwnVHzFM9lDwA20nn8iTId-qKxocO56dR0hWAzFEckwJRhaFXQHn8SUXDlc06d4jUnm_GMf-XBlwVo-zjAtOONmf-i-OydSgIqTIYzy6zYXDnvTEjY5EnF4KscAJjThiChLSdSFjqsDP7VxqpiK8ZwZl4zTbwsXKQeGFcD2ar-5Ij4Fr27eVRiWV-eoDrRQQmSRECM7FcOJ4N4xD7qoqdHFhP4AmAm73FuoUpE0nOlKSYjfo0MXKqqxsCku4_H6o_01GNH6zxTubt0oyVA01WtH8zO4kA0aJIndU6FNeAtQB3RQf2qkdyC0hvkGFb85qyIMsNIvLUqsAY8eITxNRGx1b9L5HkklAiyDV-uQeeFgQNvrhZaBUUYUNNpyTBNMZdAxkUTvL4vnsPfK9ZykDXtBIYZQVPzb3DrHxMyc8Sw0AUOZtYOW3B04bEbgZfKabpkqvQOvAiJBdfVPALfuoKIlKHyof-w7PFNwm52D5Qtlze61jAlkPta67_BbIX91ckw7ENott9tfkOKH57id9jUiJdMMOxdqRLcYrBZTNRY8WNK16vn0fqLPWupqFB6TniRt5oMslYhbaIqXwGvjYE9xcUhHel3olIrrDT4HhccMyHxg_6Q4MoZPV5Rcr4fJvYExb7Hg4CkxoujAPy5z5aVKPlOYeWIkWBun86qqPNDEDb_Tx-HF2-fbiMXFAYcAAADY6rjqPZN7kXKQT0CAWSwaDu2ntQMF1NkADV32Bm8VHkBOhid_hcoAm_0taPmdnVXj5rfyykquZRWE9F18SzATH8WsDU8YvGoe64z-AXLZ4XnPf0M38f0XNd6fS1TEaHVQ91i5EryWZHeAYajcrA6Ghm_j0uaZhE8xmJ-VBloFd8h1G4LuvPYAHS1umBclvENDQ40oJlb2-2Zen4sn7lArLWpw8mp9sUoFoudVTpbHeKnepdEpPUGJjl2GPoFOE8NWy-RCK8NhEZCMKB3Uhy6juxAimmSrtrhC7TnqYQZ5_bmZVk0CwVzX9ZKysSjjTlAT0NOokdAA--fRQRWTizHdPlnalEQKLFNGMfKRceIeZi7HpatEzMd2PG8U8ELGowu5am6LipEYS4UFvcEm8aSng3UYm&prev=RQ6C3FDE4821551D&p=1&pg=106)

* Italy
* IQVIA
* Perugia
* 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/bf0668476e0db69d?ql=l&sig=79686841d0e9e0f0383369e422312541efb95c88&e=UHiidX7jVXGH_ibVQ-NiUsUephccIJOkJ_h2_H2nT-XxLrEkE9guvVhQFH7pqv0rF_KUeoMt_vKhAECQ_CHeHYsTLEMNOhDylDkGAxZGehLQVEFXZW-GwJw4DScDl6yZ6Jlnnu7ohJkBr9_2rUY6UOgLlhJBlz5G2CSuDouJh3PXVLwOvknhdhOz2VsyC7QQpJ1-JcQDCR-y531t7dymh_EPpxDZljJQ7l5yvBw5oSbIl-kbQxBMvNfzUNsvYxuAQYiKBtfIW3RimQHt-Fr8wWDTzIrVSm7acAD8vcP8FjpZmiw5C0nzJ1PgW5Cwk4zmZgED9xOt1sOT_Ysw-gl64kNLQn9VJxl7U12ohq5UsstcQbrawSxR6weBr_IJkuhShyqj20YDrfSLNYhYCXQhN-EakFT_npCrh-Up7Tlm6tqKGDcAeivQdle7M0whFhXFk7pxVeSk6O4gHHgI8031KiYE-qI05kZJJLsZEOOCE7DnJhLcoUzsSaXM5NwGHA73mhWjqHu5MJQjH7yKXy8NA6o4QeEFbyQzJ-L_GhxMwBJFQ_xBwd1IOuXXnqV9Gr4ZAyMjAIxwNOjD6EZBSLHzDNeuWA8X9Dowb1vznHdMWJQI8i-eoGfaGZnRPmbFv5amMnTe4vQIcihlTM9givKInFP7rgBeZsy8VtK7I0Eu5cDHATULeix7n5wE0i3AvswxHTJB6iS1V5d1fk5H28lpeHC2e9RzZVBlTESwe3Ii8hfjdOvaNHM5CKrxxa2Z6vt53XLdzDdq-bm8Aj2X2xCXMmj1M4Xvxwx2XWzRXVsYQ-3EBGmA_lz8pal4s-byN-8CwlomGFd9To7Y3K3iOacWUtjFN9nKKR-OR1x9w360xsRIdi5VeO06OD4vcQsp38X3hUDM5T5J4-IQprMod-mMx7wOAsBRly9h_XNP56SEKTMXvC2Hn-eswQZ6PTL3AT6XFE9F2t2tAfG5HhsJncv85B_MHVS3n_yeeqTMXBcpMKf9IJGMgh7gQMxU5CXzGzMn-YIHWj_wtDC59sqUd8811duPmgX27pQ4lZJqyuNAE4U2HpuBWmJevCai9lybQHBji9tSxT6UfRCR06RwcJputebAGecvIqFN6GwPth8lgQ1auErbOCYkRpqHssLF4IL145zqkxAgmjOwGnY10CQBPRrZLWeeZ1WQEfw66vfpxydj1bhGD3i91Vg-ObWTV5FT8p1fUjCtKwmOA4rJbWElD_fgbiYLCYo8KKUPVN1mJ5PDGg7yJ9fJ2yMgOZgrKXE9dKIJt9wnJ3g9Ve3e1At20ouScWuTMCRn-zSbgg5nd7ZWFqRauZ0ZpAYf28E4ecq1QhkTsOqL2LE18xXfQy4ujwamxRM9Zihx7MMEJW2OlZaJFtutZFAJDByppxF-Udvnu0jXYnW6_S2CH6zCjRbNNXXjNwl1FOUWTbs4KtJ4zcsN9MIMZ599XpNb0eNRzbcPf33jHmQz3o_l7iqNp0x6&prev=RQ6C3FDE4821551D&p=2&pg=106)

* Italy
* IQVIA
* Pisa
* 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/e72288a633eda93d?ql=l&sig=1f9d7514c0e7af686ef219f0e5938f962f970b0c&e=zv-T18xFbUnkGHDmbYPq3jjy0bNnPrF2MuJttOg_MUAhIhkSE3i15qT-2FyszRw-9290MAmhM6dLoYZpXe0k8tfoX3acciGcaHjvP1z6qblQrj-jin0-GiJuh5iYefXkN6nm73nk2uaylFZICPeEric2hXPl0SmtXlnqTOmn3kRWES5If7HNUqoixdPn0DLn7juBif81Dzwwe-RTgt9uhIcQQ3x1fZJVqu7umWeHTxV9K0c3v_UGYvEw9dMhk8-TGyq78sFw2oov5cas3GtdID7rg-8vzWvGxD_yge5NZI9RF9croP_jgOvjxDpPVs_R3WlpE1_LfdKnZOvD1RN_bwjwFI-B073IFuTF-VZ6B3-BHJmAKEuNy-g_fNytXsxtzxuOJMxH7Ax0wW26tioFDM9AXFARqVxebsSE-a7YNyV8clm6O68WEDaMpsu5uJGVhcQd5E3Xf1PnRxguoVjvOr542Cu_x3AAcWLQLoJMCwQXbFIAvkxtAnScCA3SO_zF97Eaa4cIXTG-PI1Yc__ytSdjMx1VrZvyNSz1JogbD93y4nY0rsSzpAWYwjRirTBIndeuec1wwcl6KgkPItATIPWXbZ_wo9b7_r3Ck8Aiy4h49Je_6Crmb0bo_o3JLZIxZ_GolntNOAR6qVaH9dBjEIpOaKzokjDCL321BRXNBC1fq8J-K1SWOiVBXbFDkZNu9Q6gjy7hJHgbaDFJFOUOdoFBTUT1R15blPeNvdViqXbmJXGziDX5wEtnA4h0zouxxemt1pu8vS1t3cSDXCbwEmlCdnbLhqsVLVikKFvsBP4CC9sc-GOmw1eQOK92ud3iHi_gPzOz6YB5pT13gTFF7qfKutfATQguZM_uyy0JLLX8j1s0dm2vILTAFSagnH94uayHlLusQn4R8Nyc7kWc6-exz-5dvW1_mWuG1ioryLkjlLHiSI2Lkd4uqb-5X-kdAVeRp_qFCBwp7CpLPUcSl-sV499KTs7zu6dcJx-3zewSmfOIWI0otIAWHTDwAdPFvjpIAlW9m-8v1_l1UMmo_WLWg_-vHtnUv1zwBDvS1cYpsI325CWH8GwkA63Wsk4FLt65CXeoWzvjmMJEmp09gmkb7KMlKrNbadbMp_p3G2mrHJS0FSQHh9m9UIXFxCletoGy7fbnktmNZkgCMWkcy1JoKMT4RQyi-KO0EdNP9YgPcmMIkWD5BJScCOXiuenmc7jUinER28d1WkQuBE9bi5BDMrOdNG06cARZchQoS6vb34jPQBIw-gzCpR4Rc4rM-Wuz3IJgEKRL1EwNKWpNB_uwsaVIxiU1c_QOWQS5goHajCNZla1FoD80QzGs0M19tjI3YJxAxdUPcL18lanFw4pbAwtqe_6ZO_4yowIzwQXlbhkI2Z6JouVzoC5Tn_thtn_K9Qcr4Uiiwm3aJQl4tRvjKPdw492bHQEpjf1E0-VGK1NQqoPkwZmKRD-9jdTRU_D07usIhDJAGrw4CTPq0g&prev=RQ6C3FDE4821551D&p=3&pg=106)

* Italy
* IQVIA
* Prato
* 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/e9ae1932b58baa2e?ql=l&sig=4d7b7b932e69a12051320c3b565c018dda9dd246&e=k5SELD7P4aN97P2TyYJ1eWiBhCIRoIuxGz1J3ssgpGCzxkgsYFxJLDvW8aYCI1iWIx0GP90QjIOoGvhaf8X3f9LQBDOmRdyrqBShyZnY0hx4qXUgamfje_I_o20_k0rc82_pM75zqQzDpIKD9qg8dy83kMSLWWrzTl0xOl6n4u4NYHLDeatpmYyChFARgzee4yBiyYaEhrTxTzVCBc9IQqI_IBPQJFirvoQcEURNhMNsUP_am-hq0N0Y7IUacTnfduiH3s6t-137oIMian6T6iaNzeohiFJOXyzRIM65cblrRqGBpoFbZvV4vmfuV79kkBla1Imfx2y557IzspEWzah8KF-ZCN5BxYTQIa553ZwWEnHjnbeIv97cmpoZ1H7xNocGxHMwr9aCFhD0wgGi7zx-MMErLJmhu9BuvkODa_UY8-XI7ew2hTTTJXqcVK2e60N1VUp4-J50476l2mrVoy7txVyfAhugZblaTs3mT-gv62RX47-oJf287r6vJUTQlcHayM6X8LLoylj_tWyXB60f0UWu9YZ5Q-64TtQKaqvj3fceCdwVLlG8tj4opursjEh_66A3EGNczoqNBFmXPVIdtiYgRbodkWKG1FtP6rj-JA6Xjk-gNKyllWMinm3yDXh5-wVWsV6SDyojWG2kaE8_SVOBhLKIzpC6F20fLA2qDp_M6t6USWQdfMjFyA0ud7mOy4lO_a5E8DOqZAmrtOv7m99sm-EZiUeMDbGuud8CsR4tBtNBLc83r3UrU5ze6lrnykdxSGFMltL2lUHTXpwBWTUCrutRjxJoyM2FC7cyTIvhci2kBtRnbxb2rIwUBfyIwUynTWAzsFA8W7bKkr5wsSNE_5K95YsoqUIJouXso_acS5xVqAbESOqaYFkIB5te70QYmc4jE09R2aHmbRReExTVtQkt2n1K2UC271cbyTWnh0aHpWIRewMT8I8kJ6qtDQb_c8nuJ3ZbJDtwxZq_umO0d4rL9qcKkd69OMjVVX3qiA-VSeMp1olhAdtbmwaAD1_enyVD_5dMdX8gkeF_mnWpup2-3popP0VKblH5DUPGA7q2nGNyu5alAFECA7xEh8KCY7hC_g-WwL4I7yuf2w9uCKSsV3ONmAoa0jIgt4wBlNxAtTRg6fIKdmBMG-f5zNZdPVejys0tADxw9F-2cqZDW3ORqgu6vdajS4SkqItYlfFuwMMSNUFKOH1NMBaKRBmZHKRffcOXbcg-YINK77K0M1FyyGV1pyqsCyYJhh-8jHLePHcqZEFv6vgkDeySLlB7o1wir8AyWhzt3V_F-LrOsudYK6arLNrsrUVoIerbMqQb3Au_52DLamCbrNqlGhHRseaKyIjWBEevdFBwEowLZxa_xAQaegMaLj2pFFvsRmcd1nqXAy2pKDhWuXjNsaUCmzUSFLhIclFgXjz1NwkHrX2AQVAcnnNr6LAr8I__rjkE_UM-s8G47HX1v2SkBEaH_oGwJCveeBrvRhVf&prev=RQ6C3FDE4821551D&p=4&pg=106)

* Italy
* IQVIA
* Palermo
* 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/42982039a24683e0?ql=l&sig=1ab2b80077fd5406137d95025b11b57c4be30ec1&e=10iMtRphZjp6VmOWCB9HgZR4TXlZnMHFcbiOtacc0HV3RavvgHtR7lzwwK701rHZfeid23dh-FG_5Iq07I2fso01ER9c5Gpu56YeRRP2oIYh2ZfEGZ8XFk0P-6clCXPORvzHGIoWurh497aEgiL3CQuNbilV7R-3Dbsqero0G95WB1UwZB4_k0e_-CJhFOfTMJFp5OT8wB_b4PAk2jfO7lgjWZD3fxfGqJoqTnFn5VTxuQ5ZAmNwnK8DS1oWMOFkL-YFbgUCymLqsq7BV_y-xrIlCvbvMJl13yXxKjbNgqfujuTy0szleKYOaffczxGLTGacFozXzEvNto0XyElMqDDMhcEN3iHXgjV7lB7t8gh-f7Y2EfKa0Zl3zppnwa0v6k4Zigmy3paGyVrCeCPX_pvNgvPVuEPzXrgYJHoutYNB5kBodkmb-VuSKBEcZwuM4Pb198AcykScN_VjbTZCkUa51TCWVi9ASq3-Rio-KoytUj-VXnzcPI4Wl4Qw12BW-jJRy9m7NlC7OoeN9V6-hBLn03Blx0AAfPXjL9-EEKpe-rRogv2u-SRJAt1_i4qP2bjMju393oxmBqTIO9t36m6IdaJcR2inrY3Maa5GUCKP4ietqUKkYT8W_lpIeN6mKv9qdbntkr6LrsfTYuhU9NmyMDoFGosuTy1HMQINoyYogWCHgBI-Aav2KJBMrz4LrdBXc4XAisPXo4qajfh4uxZN7tBP6RWubJ1sFtzip7r9oYe35PFAitlwD2-jdLfoKL6MSFLpmePuR72wntjEoQ_smUhxlN0DNJZBGUQBr6S1HCH3ZbcirCc-DSwuMHIkO1SKF9vH_IcmSyixXdYoALfHc2pE2BS8RzNh5dkBM2pO2JUqT-V0eVmElmvlX2vjUDoUXZCsjdXXna23vvd-wFFKrFRtWkb339WXLwwfY8hgFxwCyt_qefkj7cwxN4mHa1tIUQdQL5jhfSAdSgr8erhDYDSQXB0DZ1DOUctYChOZOBj-VSRcs3TTvjcSr2JNsUwczBF5Eat-EsGJlk_B8RtIs499CbQdIzNSDJ81E-pxUmJR4Yh6cmcJHMJDiY59nGDIbbROG1xRk47dkNpEHplLieGSgSC62v2RTFZ7_IRHdrDmjgSOQQsQbmAJL3_lQLun-nGxcb0m2Gn5ecdMujcc38AJ97w-glad0iS1XefkBKZ2gINcaraCNXX_7eVA8cPP1-f16jyYZIcxec8DWG9mVqWpCcOElFwCFjuctI25yhaQ0BQunk6fsD7zwt72y7HyvkRKv_uBhYl4U0zX-tZ3iOZeNaDz4hxGlW8Ibwz8SJDJzr8LFHZBSVdHmtBwAsIEWiCAy4B4L-Pa_Ehrwhc-gUBYbIUP4op-AqfM_kB4nfZRsRlpfAzc4O_DQIObxs-VD7xapeU5LzIjj3TrVIuALEBgrX-QC_aGqMllMkgcTxyHHIq6XOvs3Hryyb3zC-tJrm-_7YDplwSha3mz55JR2w&prev=RQ6C3FDE4821551D&p=5&pg=106)

* Italy
* IQVIA
* Cagliari
* 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/770b8d35b89fd122?ql=l&sig=ceb5e8556fa261efe465bdb84cdc4c4097cb0eb2&e=inOBGpe0vseBlJef4MPBJ1sbNbXuQ7-AOHe4NjKAB0-SsZBAHde2CS0c03YByoykYjDLOyGB7Y4AH01XLUzJd6CiKIXGMioiy2iBYyRcP2l4TQK-R6K2HaCnJoXZ0JAuymcxrE928a6IRc0_IId31s3Bt3KLjM0-UyAhQA7sHaGpolnpemaX__HNL2tP_sArc5379FeeFE8FeuzqYuDuSdvYFM6wqWAzCblT89wC_x66wBR4iHMtv9ngeV6aPiY3EJwGoRU8s7wsrPc5h52YcSaWwf6Zl_4Mp_Meolfe-1eRSm6zLRtgiFHOMesJYwHPwUHhzYi6Xh0HiJ-6IaUiVLH0roLrsVgeGuB_tmKLa4aN30_akg2TKR86XeRtQgzqo6Md9ptjFmsL9qtqwPwj9CRz3hgunTmNtWDxbXq4DNb3jmXNRQsAd2c2cw475Nr2bb0pDTASaEz_yJ2cQqdR3V6LYaYIlxJo5H7agWl7sPJDiYlY5L736QSZ34qmzbrbXXevFxUIK8YyQg9vRhgcMgNT7nET94VhJDzcCOThIM8rY1v-KAen4Ce459ISKFpsT68vUGOE3GoCUNUiPvR_48i1f-uzRVad581YegRAv7k7ah4MeMdm6aXpEv3Pzn6QAqWpHllVu4Zk8vN_Yto8084KigBoFYsFlrrMArPuUPcKtl087BmWtKQYZV0d4YppwWFjjaC_OApsRypT1NRoyHPJ3RYpHpjec548Ce8rKUAMfyCXp9W5kFOrQge8bUvLR1WY925OBEM6BXRSM-4oXpQDF-wuEFIfDt3bvKhEIhB-RMUHURHU4UgA8FAAxYayoKf6CuaTfAugk2E4dQM0vUs35ldfkYLEsfv4-S3skpL8jMppSN7zCczRdC7tiSrvuDjWv1kiRErhLLkJYKNX_nETY0M5p6Xz_PUX00jgbNx6Z-HrX7kQW0z4UJ2Ui7zIUdN8jYhV2-yOqBGhP0hf6NtoNGl2SwtB75g00jbAax-RcRqeexDQcChzdveizTVZvt7Gc51uEx2k_u4qedZX-4zzsguASSGsl3usS3rf31oPiBwecmW2xRuUrxq9m1egkEtUlBehofdVRbfkfCT9XoCKInUSnxgWQsCXhysjNIOOb8vu-3CEnO5LxWtv3ZQRcqmxd89tv-_sheKNwOqEih24YTlfC0QvDzglMy7nT0iipD5AVni_XtE0gDDV7LfylocY8i25hLAsSBSBQu7geDYoKq04eFD8GYSnwnpPEQ3TGytl8_loVv1Xej5q7NPPyIshNDfpfJH-LA7OkOLYpDhFYmACulPFLsggqarIE7JPsr9hNVL1uJVbsyNTYAyRwlN8_0GiDeAEJ1gLsPjg5RB7pFD-qaYHLgmJKooW6IIiXn4OkzEOP85O09Gxm2cj-VxLmmZ81hPVhKcW-D4YoTZPdrcUQYDHoL03LZlUbmrH7ihbnY82DzaEnSYamcrql2Yr2RPv9cOpPcHQyoKB5kaF&prev=RQ6C3FDE4821551D&p=6&pg=106)

* 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=mG-yy8HeMyjTO3QKZXlslsPz1xuRBTlCBo2R4BA1S3dVEnyhPjh6rkYR_AKFpMgNLSDmvCux0ddwcy821uJOaBA3a9Z7ODLgODpv-GbkBiYSqX55zryhS3JSEcJ8tiekW9Y-Htf0CcUyWcvblYJxbJJqRkljTxjtjYLu5DQ_UAFgb11O0khw5eerbrIfx9C3qhW11-l-Y5loHGIRc1q0Skg19d24tNQAGssL85h88XNPhkPWccwMccKR54ns_PoEH7g-0ycS6TDoG76PhekPP-yRsnhd4Cu9Vy76sCRpbTMzL90pMNwjv5LufBbkANjXJgt8d4Ddntc9-90bmob8lBdUcuclHpRAyb11OSM4PPzpjaPWX4UNz6gz4_mv-t71yTOlj7WepXMw40EAAR5GcX4aNok_ciCpqXtgVjFSdB-FlEwF_z55YOiHEqdokjrIGEZSnrq9HOFOlb9ZDqqAeHsgnVj1HPRyHKMuSfyPqeJDHxtGkcGEnKitP4acFN_VgaJ1G_etkDc7LL7oKFflpVX5xamfFJzOz3f8aj9R6LvyGjXBILrFTDjxVnK-ME2zYbfXi_83WDABBT5wHKbDaEC5llXs25IJYkpxJxLm-R_0-MM7-aMqDjQlUeWIq0eZmbQfXUqb2a6yA6fqhdiTfcT9iX4kA63uCSrb_u07wPsBFeqBSdOzUUFy-E4846AP8mU-vbQGK_kCX_4AfdPxbhUKh4vDFX4EKea0_02t62C7GvEAemfhJKlsKudZHHlwXu9W7ST88LQ1QBBuAnvHxazECaPeYGE8ddAAkwkTBgGdmkfpMpsm6E4g1J9W_FR7FJS6AsVicjzy9y9ihRgrHOEbuGZ5UYW_q00_9EAUB-9jIgpkcvYQug_8BYq7-YYwk3gV2eeD7q3H2AXPYz1XcSk_PAJyjsA3AaPN3Xdkt6haFJbBrIlHvLGVIMVgJTiY_zBklANOfOnt9U0nQJAaHoEL444Cw_S_6zOAcJG8-BaKWWKH9ZRVgwKPTp6Bt7on9t3ZMJQgkCNVhNKFbJnoe8UTLJcisZV_weGKJUQJIZuEfo4JcViQ3pN1C8JhVvyp3m9ZaJW7zwGmji8i93oZMs_jHCu60B67UtKt8HYmWS-Bu0qyL1m9DZaQuIvWsIMRjmNA8BpAFvP9A5neRcK7J0pzeVhE79qycJONtgkF8pv5rgsWNwzc0zP5meaQ98hhoL9Axhj9ZSyT9UItn-KcGrgqaXl9_rMz5Fjl8lKfjSJZJGiDsBcVENfkUncFFF5xLK4Um0wrK6_9KmJaHzG_ezM_Ksba1-dqVNesZQOONZYQH6JRq7FoZdP81sue60jU3dae2JWlLNGphFGRhvYgTHSGTU1XnCKfU3bo1yxSApMD32RVNlC2pp6qHARptCj4C1IzT4gxEA-ADFEaldo1EhDZ6WgveTY_nOo-DtBUn_Nz_RGpMrNhuSJO2anz1lgAwbeV05tmC1CgG-6RIF_Y4bHo&prev=RQ6C3FDE4821551D&p=7&pg=106)

* 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=vtSDYWIVUtx3GDOgbOD7tKb8eSOqVo4nZhbTO1hXal9N4BAucwfM7TbWLFBoIC1L6qvzu-hd32L7snPRqrbwbW28e3ftT30LtAOO0frjKkOCmV1iYZhfghBLoNNlMHAOx0VS2F5o8YBhqT0P1gxViexsecc_NK02WjNMgGFSdj4UZp5X4uuVJhIatuOuXOWkNTujgOmixjXDm_ymEO0RMNiKB_LGziCUbe20cdVJjPpiIi4ssTHSPBmVpbdETkhP1Dq1Sgm-NM0cV9Aw-OqhvXuRrVThcdiJ27rxt02tcEKN20rIPApz60w-BELiGegJWPjEx2UPEFjzkPcQcwG-M4u-OaXORdnqPJyn7BdsdLrsJ91HgBWDyVKQTCRjEwfa6OMFWFsRt8gVREO2iPt1vfuunBGj0nehI9N_nSDbnMlKq8V7AIM96r7UalgBTfTbRsh34SMnh6s-ieMSire6IA0aj99LBTi6QSlWOkVQhMM_0SB-1wEgtCsT3jVa03O-a2_QMrjvn6NRUtPliSAmN2JWpC1FicEo5BnQWt6NnQAhMXsXS554O1g5JgfW9e7z1xBDRSiKDFe2QP5xQ8sKoBsAOuRWJHc5v4vBMvmOBDORfanRn9U0c9JXsu5X0z9F3t0oz1q2SxHK1e7gK0asjWcrtn6JTimcd4uIc0ZfarYMif5Wi95W_1vraMuikCdGQ92gHv7b9zpKpcBT6KC-C3FXufaqumMIdTq5HLZF2m0MYR2WyRzuQo8CES208FBlin2EKldCYNkrAGgafbyvtxbTA7zyJovwrp3DQEFx0Q77W7MCcMPwQqlPleyUynyI9x5ejrwPGQYVVrrwNu2Rs3ttMyuWn4olFOeLHC5n_h85hz_tL20s_VKl0MBxy_ADa9I3j_9Vmobw7rM4DiDKfd7t7tlK2OU623s7lotZ6JQHUewilDYU77VHOUUBXE3uBJ4gCA9KuHxooX17rLtdgR-Hw7cHwcByciM-ubF-tEsMFZ-n2FPM12F9DOHVJ7adxSZDRW5EdAvxUDYlkTR_F23ahRBTeAMnpiMLeEK56G7QCSFFLmjwkFX2c1drIkBJArQbu-_eE_EdKYnQnfk52IR-4khQp3Hl6Ye9ZXiAlFr3l8FoOvugnGfdbgncxbs23mGQNKz107_OSBQeEvhr1w_QIx60-6ZoS8kfqQY3R4cn8VWuTMptfQlw3dCx1XQyJpWIxGSrfYSP2zVxiflUK_CseMGHO4fb1ewcDlvndZY9UiVAu5uNx5OCF9DzqiaQ2TYVZNbP_rL7XU3If9YCkS8grwGkTUtPj-yuZ_dFkGALzLfJVcxvKfvzBqujLqUVDeanJ3NfTZyxNLArwz3sKPUbDP4W4feLu4HOdssCyuC4ByqvVBN7uZG8pegn9YyiCxcIlcqc11Jm1jJVBZBp-iE5ZpsqMkhnN5pxaqxHVHiUuk-03hRs2H99OzA7MEaHTuyCoKgwCpRyGlTCBO2Xpbv3p8YUkA&prev=RQ6C3FDE4821551D&p=8&pg=106)

* 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=kEbv2bUq5iQUYj8GE9qdP78j1w1xN4VQ3yAQdtuD6uLTa7DIJaXzRHGE1sz2RgrVI53Qnel02TfaDclQNU9PHKC1pUhMpiqWBGIAaUo3AdZIrDMXKjwsbYpH08PxhgwyPceZ1E7b-dPgaHQYhz3q_g-CsJqqPTjMz8GY3uZ4xCTQ6l64KtE4r1Kk0upTNo8AmmL641izGEa_qYOtPitMfiY5aclypHlqiE9vx3VpputeobmZeIxWkFXj79tL1w0SKsYxLotLA9ZFQeY9aKDNtI3M5SX61nrXur3nM2ZGttwe7gQF3IAWyq6byXN4sgzN70nwyw-vBpy8WyTmZAnM_dNVt9Z9aGsJdHw1xCR6_ecSfLwiVJzfni_wCzLQ9cUWTqtm3CRYxCExbmW0AywFyr4NTYrBniIl_lNN80Dr22BJ4skVNzJ8AridrLNXx8mbqRD64yr9QL51G9MbqiOQkdhoZTG4uu_7olFWGN9ZEKh-Z5ZRBoqOKhqtABY3soPJVCIcVd19sI_z-xfgN_GMMDlNDECxB4N0QNT6RCWD6sPkDE6Lca4N0UXZczigvAvkggvVvCg03z1jJ_nH4W7105Fh7RYRZDVmIymsv0uScrOp0rjrNkrePdKDOZIYt-3dvmeI0fRnEn3Oo1RVMDTbyYd6Gb19oI2CdK9v0PAr_og60Z4vZEFHRlR6yeTzfg8noPv9pAYmakemGgBQX0SSCfrJVkHF5U3j8lu1VSdKnbXh8HKI3JaUIHRdyFsNVybi24gMspAF4-h3uTjUQEVo5EMB4fL3FBWMJePI9ZGJrvAJtgJIiJbKEG1li26PxWt27QrnJYTDRyJOBQuZkCjKMTvOR5eJUZa7lXpzL_1j_lCCSEU5Su7wO1i09vxPbQaYdRb2x-xnhxzYqRqpijMmwM1_OjlvqDKrN3hYF-KF2WPrU8vMGmxa3mdZdPaP8iIg90xvvfVzEdqNasmVu02J5FJdtBdt5W0QAE2V_5zdXuNV7icQDpTJx5yRJ8P3m-gMw9_iSccN4Lmc-Zptx9ETxn1uEsQEZRYFI4Cg-w7poS24wii6dKCZpr19_TQrnc27Bar-Wl0hL2ciD67GGwgOzWIr-0RgMZaPZvw9fRZei_IYj9C106_vCCSz4X1hWEEim0iXnsd5g2Lql8uvDA_E6ABz-o0UtOdPPi7zOBG_fIyA6eml-rc-yqCniuJZmAbqbkN-eSFVu6Cnm6IZgkvU3Jt8uAXsqvYpGv99SoWPPOsOcPcigLgYK-2aPGZwfkWB3hBKzh5mJNqrLbA14RZMTios4yokBQARIsTTFZ2VEJZr5M2NO2o3kDuikbpV4ePP9oqlJFHU6GXwMZTmJEglC3cRq9bvb6z7u1pbZnVzoDLTycOdipRiO76lHKRzCkX_A5NgTRZpZ3M9I6weXknIS6XI0NNI6Vgml9LXutMsaU1AfOo1ti7e8c8jTtskW5ueRSi5Vk-ZLIMAFAT_cTKnPA&prev=RQ6C3FDE4821551D&p=9&pg=106)

* 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=2f4aA63t3n4O4ZIh2PEvSeG1Wx1C0fl23tbQQWm49xWbx0U2w2wnwou-vZZ7b4qSdZnkggb8tRKG3DrEOzIMLU69s6sMcGcia5UMm0GaL-hVdYtpX96sGhG7AfF0oIy3GAzo3_irTck67hs4dsCHcgC70aX4F2Is9NT3VrTrEMmyzhdv4eHM6lN47xTTvMUJqDxiSmOdiJ93C35ytqsgvL-JFzhxpiCjvDw1nbDWjtprcEgkVT1alUyrEUkQdS7aPKM0I_A-3p51fbl6OoxZxLSU0_SCqJ1omq1Hk7lksOruFVKv_ce0HsTnTb-AyJIWTT_79ut9wnRfM9ZEAalYy007QNpGdnbbxnMWt7UNEWfqg90zQY5udmqbyc5W1a5owBhYaW4iG2QYQctdups1uWcE4cXD4FIkpqsLhowh3yIxVbpTXx61jbcxiILzHKd57hpKqUlvCyP7KCCXNLlJNxcI_nDZXSiO8kN8vmLT09kXHZhGZEi54gJw3FUrZH61khD-1hSyj07zxo6gAsbHupMEpGqHa7qEsmO_XyClIXlymzJR6KtJqhQ9WmAeabontkRpDk30lvEtIe4xJq_XKaQ6yLU6FVGsYz7IkESdsLRFNIEXFVcL7_dJujet5pGQyOgUrnByPBr2A67jR1uDsmkyZYYgn2YDpxNBDGkMO3NEL9IvE1knhKy3SZxTNkuR6K3b2nCAy9q4zf1xdPeD19VVdgfsELOr7MZ0ZJv6lji74ZOoG9wINEYE0vjyn1HoBcMwiRNGKM4oarE5ZT1_8rphuWzg-w31FhBe2Ozy61oB7ljgnPq7ZFsOpOo3V5oZl6z45cehLa2OZ2swxDK1WOn6Oz7NUhYgg1yia7zySxoV9cNahcrdIpYiWcsAclYhDQS1QTKepLlycL4gdky9euLXOZ0AEaoNgDY684e0wTagETfo0tQ4aYLjbovWAe-AlaXYyeA1O9Oe4ezaTbeLXDVv3nkTmZ1eKBE02lQeR1TApm0Hap3ZxfiAwxmRz9lDCdWyHwp3p3LgHWBZcKCKAq-Zw_KqtQHjUOepNVpOIpPxk8EwerpMXBZLXQQsxi-7EAi0ClD7afA_pdaW6wF3Mei1cJT-6KbWInfFS5jOCaAMx0NY3__CxulWK7LgsI_1N_ELJLtfq8aXsv7csP7m8wkoCvvF8H9FrlfVhh2McF9I9k50uE1zkpRWpC43bInrN4IqmA2q0PxyjTTD83D1NK64J8FUvPx_KwMfuu_8FpkxokuZwaTcq-Srby99AJGY1LRvI44dYh7xW3hA-0hLxix95lfkH-xUlRCAdfUqEMVxxfyF4BpR9VDNlwI_Oc0sL42awclFwYBzhAEM45vQmbB0Kw987LR4NwHWcdUiQ1XOgZG-jm63wPajZ417oA12n5YHjYM9u_rQUXiALUywfpPfTw2uxwxExAXPTI79F8vYdx-t6vV9MQQ8eSUXCYBn-GZWhBhZ7ucE9qrkI12FYuI9&prev=RQ6C3FDE4821551D&p=10&pg=106)

* 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=hsm5Ftkx5I9vePLdMVvFVnKVGjiaFGiR_tzhh0cC_rs7ldPj817a5Lw-nmzFO2npAsotGkHT8dP0T8BFBDByABDMj0bIN3ifOUObWk6iqfC3o1JK9NdAtgXKWwKOxkjC4ird2TGA_zfGeeWevcxo4nSdJSzzKNsi1Cg9q4g32sCS5xYD13zaFfxeRERvpYQwAhOItPxgo2VOWomO7ZiTqoXgbKOWjtGrJyboV9BFaalCgAWU-3ma3Je3vT0lhyjXhgTbga1ussIpbTWCbVtb1AKUP69YjEpK1LLqgkyPkDRtAbxbosvZXT-2fm0fCqWAaAe6EV_xe09UwyJc9VReGxZ_E5O39LW7kP5NUXlljKDNBAYo1Qw61ih4NX_n1cPE6ZB0dCWR1FBC4Ea_lgrpuwq6g8b0_C05IiLcc2P2G5h_aM1bynfj6y_bOhh-cZnUoT39McfZl0MIbh6YFZ0_WYy3JCrse00IxIBwt9Fu6ZK0A_k7uywIXkR8Z4AIhrv2ptk6E0vRXuiEcaAMEzUCjD5lhVaFHEN7ZbrdObvWuvNoRwlvzgpSA4AXyErn10otThnXCCX2k91hs-qTwhJwqTqqZWnk8AlA_0RlzLpPybZkCr9YtQM_XvX63FtjvT7_STWy8TnvH8dIvlsw6GWrmU8UF_tRvL4lMt6ufzGuZwywEsGBUXWChVd5tvY7KTuIq0iDmuSo4LUuYTufLikCiq7Gq5_kbaq-PbEgG3V6swVSwlDqnaZgHkoNPVjAW5vJCXxfKKz5d3X-dGD-VKrXlDXkLnqFBQT9StweMMRXlr7L4qote3PW9lqoM2FeROA6UsG_MToEesWI-4WXKjEUv_kw5wtu74q_SRAVx5cP_QlDNu46e_raeDBbFUeqq5ojecJiFyjT5h5cysgXidBeW8Vh9Hv6pWaBwjrN2Frqoe8N0G9G7SjkySpBXxhEEGtgXbhDZFHUvPMOgTPkmaSNjsXGkd7Jy5boVpoaAe-n3YoVwUyORDpNa7P9ls2IfOh1Ddbehw_RP4-CcH3iF945zgQZzg7WyY1Y4VdNhFUQp9YjSN8L9lwVWqg-NkDf1hUlP6-4mZ37hqrnZ0SMLE5D0LIiM44NFJHN4zfM7UvrXmXMV2zCPMlhMO0xCY9qDltQebf8PYvL-mVXX74cwmiNXcFvlYeJybf4DjzZAuBGZOrLCiUbLkFg7KfscO3uJ77QJFxBf605xs-v2qfbzfSCm8xZxW1AKor8W2L5bDjjGZRROs0ThoVJaBKNZ1Aub2v21EmRggpBxhS7HLlFEyMayEL6Q-sdkxGWWm69laivUrH9jHQ8YvzF0HswFt4Mj1L3dzYoTFgN4UXs0OMZLQKA6SlEjuG-SekogJV2fTrzs9nBqXU88SmLY-2U_ZblIRbNa242ZQNEFw0leLsj0szCi1w-q5PKB6Nw4JwVibcQwxTWg--ecRL0nuLj4DeE0y0u6z3inF5UpaoXPoHPJqSN&prev=RQ6C3FDE4821551D&p=11&pg=106)

* 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=sgtAe7wkEXT7djv8LwoKSTJSQDFcut42CzWKkdgvbow07Z7P04Sf2nxqT2IC1tbtiNVQfT-a0CVR8WoqcK0FVUbyEN1QllPyxyTTNjH4HjTHym-bhgjfq1G-E4gPL1BQZExEjFfMKEQMlADWOvfF0H_ZDDUajHSfc3avqXSi0oCjItRuE2WECigYPqKGom2dblRdkCivRlN3ZnI4ZiX-fxgK1HnZ7Vr9ObSIKqNsZQVGH3IER5vGkx4j83jp9SlfHyDOrFCoSnfK8XfR9ZI5mpdK1K2CHG3Z4VAQXAuDfNtyxKM7n78SYxDW43Td3vqvS8V-mPtWQTE_VjFTCprOQVuUsLhehiwJl13GjD5GLB97cFnXquMOl0SQAdKfm_ofQu_XeYcnVFo4xHQvrlgSvx5fGSEf47SreoxBSVSbgmh4wDvXfWhP9COm4uGySUgmdRZdbZisSdq-8ktwNvwx68t_2YDUDvmSfFMUhiDlXeRuQbrl4kbMxme7clvtvLiLwdMkJDLM6ftdtHzqo2MOI-v_artO99fDtt3gYBbft1Vbpc_U0S8LpydAANbIG23kyETG7yldnX8d9egeVg12X_zVd7yLyLKQHABix09w2j3fWyCdL6ucWjCgIawNqBJhN6IjBRwg4jZ7fbQ1wXVb8N_cs0vwRxUcQYwujQgtmqk9f86of7S2vRpl4Ot_IDldWrvIVpBrcAxpRwhUTSI0fkXOgPm4BOcMyWgpt4BlQaiCPDMeAh7dQq-MkN1-XyVGrdRGqqIplnpmAJbQKN-ySriGrP6USQQ8Rx9yLhshe-1orTT6qV2xOK1mdrLhxh6reIUOR7UN8SpX1d0ux2YPLp6pOz9x7mOm9WBlFXaYmlmGVazv_wU8FfjcleoY4-A8a_-vrR6vkr-GummbO-0l8XSAUJIHcLfkTbfqLoqDMJlTwyUwI7lGkSKjPATx_otkieO50CyTDUvHYfzB6ZUPTh7TpBJiQVnnae_7DmTBX-iOCzcW18n-LMiBG0FrBZHuZ5qbCzbC9sBPn8NYX3yNhTkzlW9shylNSEDe55MOp8sykZe1VZk24srcunmOvHjTcwZv9ieDRKi-fIC4O3IKMYtaRpn1pw21FjoZKiW0-JHt4gfZus0k5bW6OpLohgdMTD-j-F4s22M6fyXe0r4V9G0p0pT6lB4tILux_o-nP0GECL2Lbn-F3HLzZl_AmfbOK6EUTAASK4u7_I_ZZqAQ4NxrUfRUAji3c4V23BOovLTzac2rZpvmkmjWPn6tduoXrso0uRUSIERwKhUM0uFpF1hOlLVyDyVr0MNsokrnKXxqayccTw-Z2qRBCcTkA3o1h8xvkt3M3ew97ic7ZheyWTkC52CAenu8Rq9D3G2tRsLwJGooeTZXETpej-ubIjtmN3vs7bA2rz8pbkPoT4yfwG8I4WfzkwxuTz8ymxjZpc-8oqRgKyO-lfwdVaE8kxmvJejljJR8ZOwgcTVpzWTdgCl7&prev=RQ6C3FDE4821551D&p=12&pg=106)

* 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=oc8kox5Kljuhg5DLzX9NVVPBTtuVxSnNbFupdcT2e_EciOVIjfOu72iFYZlE4diGTOOzoZUzCOTbfFrj-Yl9z0PzCHJvZptWHp-Wy4Iz70e11I6OR4Fr0LijIYDd5aPatWGL8pekquKwCUSOZuakUqQDncG0_usRBdbis_0aPmM1PgGF3tfNDWnpNhDTeHfpCvRQy2iyCvurup1P8Kuxwgue37SWVfQO1k_yiPWUEU2bP-7cECLTDM604-tOCxmrooWDRUhd4sl29aWoJf-sWCv5J66EPU5aofh7bi7Pt9fO-Pmu82e9Twx3qUI16h2eouIuZOoPwaI_n81it-E3iIFGKsI4NP2RbFilfIwBv8INN3SDVbA73gWF1vV_-AT35i29AMPBEk6fVeMgTmcLNFbzP9KgiIXLmFLt4CaC1Zx8pCLGvxfr9iP8jHnIDHTx5uo-oSnsTn-CS0Pyoqe3ljk0zHyBCOwJflZagO4hGO4KV1-2Ho-__Pe7tMUULoJIHggBkQgYWPPRQiTSGzoPMWbPLQKeBK1UiXhRDj0J8GIKMmhYzIQl5ma7iMDZfsxl4Id44bbZwID1wldUrE7bsNk1Na89m4kMyDbdT2rYtCB2X-c26p602b9TCQe9H8IwM9Ell0w8Dp_IjZkqb1J7VQWh0nvgCPq-NlVWTy00K2Lt9J6a67fq_eMZGEmec5_DhwLHd96WmMhjOoSqhohWDPkRy1a8DxDdvroa2RiPh9c100WcR7T6H_hpks1sxqIY53TRT0L7uAJEoO4cXoeXL4CJ9RGOBd0FxMYWYwSBZtO6gtZlRS0pr4QLm2uoXyZs_xhEGCMjG7v4N5ibP3DhZ0QX9AmHPXpheNU2xWGKDBqeEe6I8SFiaEeeX1wlPgXE5sL_ZRLbHlEk4OIcQDYxq0WDXq0lUnbYcTa5Bupa9w0ejlES0klSUamLYn2DvOmFRrTzXWy4-bIuTrAK3YJXFtAgNr7sl-SLrOl4TjJZvS3ouNaEH4wXTSx-DLOqHhX6SSy_DEFEe3loW8FAweyr_yH0toALVqn3BQPCzdFVV0khDLafkNgHUB_wakgksd01Qa8dAwTqbaNUf7_ozGBi0cgzFi0lzCs7yPHhJuW2QWoFei5Fkzsoo1n3YvHtFdzyFgEIIBdUwfslprdT0Y1eGQpQ8K8PgV-6N9MV0uCcfbQ-wosQtC_2O9AmRtTkIzkNpl-jCBDuvN4WEBFlq7cUPDGvFg6dckyAHfR-KbHZUW6Gwg3CbPv4nufo_H0jTQEu88jgF326VyvjTJVyW3cz5mUrrXw9B9HHjIzPmqG-yl1ToGRF4fE5UE-rWh8P-gDg7NR2hEDnKqwjNBH6ZfM9lJR3MBFSkD9fP0AaVSDpnjExEFka4Jmn2ZcfmcnC7jrp1rsvA_YAT1ADxBljfCfUdRGbBRGYg4dyyquksR0w0e6BABNqdbCH-SCFx24bBUHatDcfO0GeRmqZO1E58Qn9l5vlWiE&prev=RQ6C3FDE4821551D&p=13&pg=106)

* 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=rAS5ztS78ZDCFEb51D0CMHWrhVOTh5qKwBbxHfqku6JP8P00eEHxuOqvyr3A9O7BHsmaVtVeF9CaBn2qmGKi3jsV1cbi31FL_WbCLq2j-o5zLjPaRTOUY5Ur-uUsAES6k0ihPyBOCgPQw52mmRhOmPh_-EtFbNrO5xZKy3drwQFL8q3mYIC3lHBpHp9MtoxK0oRl0_uNGtcaghOqFcrLMBHpeaf379vF3z0nMYdQS8qiu31DCdkrvqdMNO3Hji1CQSQ8Z57GFvR9EFsNNIlzcs88SRQxC6dRYz3T2cM_OUAOtwoszEe_j3JBVeDJyOU8yB4QHIQk_ZPrJhhhzx5eI57Ijj88NYE40x2O9g7wn7DknWNSXBLU83NROdDGjv7p5hAOxYnYXz2_IN4HYoBB1w-hd8QCDlKDBZ1ngWbVZaqowSd2-w1zco5E6-xbzrlYis267usZPSGz2Xc6ViXknulhcn8rBK6AZAuZUOTKJdIFUVjXDCeaBZzpGM0ALMw8owJ95STBCIDmgndPLSVwHBOzW6fTXcW73ncio9iqBUh7KUxOvP5qzTUbPRO9SjNm4IkV5viXbRAy9SBze_PHTU8XKRrhVyzX9ZVmcgBgppHD_r8WjG5z5laWVPT_FTuB0cwWleS-kg00DKeMGDqy3c_7OMVvnLg8mfMmyyixeB-xU0A3chqouIq7h0nGEZKSRqY5eyzd63MTklSHVHGaW9lNdQtp3cq5RHhtMOSdMcdPOlnIfTfelR_8ypoHcDhIo5AR4b_WPNjCc6cUia-IxH16t9tZW1bcDVyYWOiV8GAggcLg3XUQDMTUWBMuia5BC8JrQHuyZzNvkjs2cAjt01QKd_WuNZQKFN74l2RrFDw_WdzjQgmO1OXMSgi-2fWkwAoxp2E4aKol7z34g-wp-DsIXNX2pMZxOUgJUoTdMsMnTu0jHl-SdY3xct27P7QUtYwq67GExzL-YmG5xVOedRbG9C7hKVz89c9SNFVHxNsom3K5GywawcTGC9ATOiMr0TTmkO3CA7NMnC_lry0KE-GwI-klA0ECzPuw-GKR-SgGHtlYp1k6PCrqStQ3fy-hHx1TRzqnqCL9VDvCPj-eWLFOdVURG583EGHhw0afT6lXdOGlRUag5mzjw8Cvq2UokzN3c873Ze2b5r4H-m1ls6BIXm-PdlU_IDMKPywBjKHlaZF4skEc8m5XuQh0qSaGVcaSTViLvnDR8q5Ft4-YKWMdMSha7EitOZNGVJ_rfGxNotgfIjyeG_C9Uq6r12QVi0NOxbZeB422oMDTARWayKg62ZTUxGi6QDayDLLArqAJf89vDeQTG9e7w-ni2fZT5hNcri1n2sTOFUc0ArDaLn99C5sRn0BCQq916YFQWndrAA3Cplx_ejiExIHvGZrChTWGfTP7PfC2FAEwAPKOnFKEKfwgaFDbjNcIkwHB36gOSSoejFlt9hwAOpVEE404XGhzy5i-r-uecyg0wQzrdBYH&prev=RQ6C3FDE4821551D&p=14&pg=106)

* 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=GCAX2wO1EKPA-FEycVq3FRLWTHUfhbiN7sqzf97QtVuz6bz-eWet1QwnwUTHRwDvq-vRsgUOznMoIoG8Feiqj5Fm65TPg6haFEDe7A-ZD0v31ukLSByYZrrqeNv5H3_ONVGtnhuL7piGs1JAhk66d2A6vZlgiafiUrJDjmZ1b1qWpaGQ6zPMhATBM34Yh1XaWDlHKTNkHWg5n5zNagA_sGfUMkDWZy7GfVCL3kDBrdxgtCbRcEyTJ_92Qhne_-V_muZduxFzUOFLrXpywGu5lYmhV9tb8xdcEDoWZ9ORUWEL4FgXaJZEU_JS1FEdFaPevIK3sm6ykSITMfqrV8Njhn1L6r2FQl_enj3z8JY1YDQH3wcpsuuAI8-dRKn0buZl3loJo4PKFrtKOQLL6geNQXcYJ64uTbekvS8ZRuSC68a486hoTC3p-br8v5C7-4qk3h8-X-MnLm7gtxrb53lJCZyI7RGs-KjFXFpOmf8_pHGtjZ6Tj34wvcR8aMxQaKulxfoOKBxa_xpypldR1jGR8T1-wizq0Q_YnhbLg8sUhAszj6TprXBl-oADmpwyTFqzp04TU13b1704pboSGNgkGyjRZGHXZyv0JVbmnIG9-5r205xoHH1-e-qa59vp2dSsTXcmNrmgXSemT9Tyviqn3EnEYvSpCKaTv3FVfCzV_qXM1bIRuYg0xCXHrBFAo5AiT_vId7SN-g8_DvF_Xg1OGn9eyFYnDTQN5ax5R2Na0cUpMVOCchsM0xM7LymxilWVf6OoEIvJKGmkbwEXgbUCPTz5FTfIsVZbiXYDKpy8GqZ28HCtE900mE1qrH9Q5w6yiODmXXva4szgtZwYaaolVavR0x3TJSd1q-4VoB7eQxBf58GekJ8DJrGoxUfVBz5t9MzzkT8x-2D885VejcHSfITgK3JC01Q6kEf4nhVo33a6D1v1ITcyFDc-PFNx5y9CFhJ7vSZWhyUbRPEujKcX0BGdiSewuBfZM_607_ULg28IksDPZFbbWo7RcPxkYDSNicjVNDOcHOCQULmEtmQdSdAO0qO1l8fBWFqL5KduXG99dZvXAx3SeCxCm6o8E0kG_V8qPc9y5DumsOs6a7r4RAsG66EWPULoRdKr6L1Bktt6ZA-PzBPfc9Hf93t5apkU9QoFMHLuSsmcX6XV9Rh10mob7NTxCQVtdxWxtM7JKylxRDcvhePkBgv6JNecgC21p1M9Vt91BbnY76aSItb3uncqS8VnpK4Yw6ocn9nHHMCerJNSK_2Pa2S_dTOPKkKSictVL6v71fmdvUobr6qGjmvOSqgSaVMGFCdUkopm9fbX_4YMg-SvESfdQFi7tbaUIzYXAIZwVgYYPduJtImPUW72ujiH8PShDGR5ZKnW-Zl-9xzLlyLTVvpjEetLLJZY5ek4MW9jKLNjZygDvLGKi3oReps9sR8uwFYFKMMK9lv96WKzUeJXcLgTT_04nzOwmTcLOm5cGw24YYAuHSvoNg&prev=RQ6C3FDE4821551D&p=15&pg=106)

* 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=4-xHVjeJ2iSrVb9xlJ_KOhjo-VS9FM1Hi2lZfMKKtjmsXa-BR499riNblufVCfpZ3Q3n5fINfg46remGmHryPl1j25QmNMOjoi_ZLl8Tz6EuCaDSeWne13CaC_wZm1ihqaVHkr1uEtZXE_mPs1SnHajQIWszaFoShfMy68Nu7H53QJ4Fi30DsGDqEyEDRH7bGsR-xDe9wD0JSB6mydQu31Oc4UhGtFhyTRwfRUirnccugcVl1BDTlJE5ZDwcb8fJLIog3DlVDvbk8v-Fq9cg8NtoPtp8mH2WnZJQY9mYNrG3hoaHwrfCXZ4y0-I7uTedLzo2mz9SjEFe7sDvzUbhYzZg6gAeUQFqL9nQjmJ2elQbcB7VDhor35_WxAbH8OXeuXM9LEDbV-tf37h9JgbJVTibmwJbMEeMaOgUlI9_bVPVSpJyp41Z1656UrV2LdnXnz1Ys4r1mrkG7N89-SOWCzBDF-e_7THmtqpOSCG9gM8_fnhWdoIj3FKZVDGZF_ONWmPbm50I7JQ0mghX8yF7j41SLVfIUmdOzVwqK9QVYvactMmOObTe4l97_EoY103Cwdb7_-Qvb0DELyTd3ecXqRiyzSB_jpnH9TOdpPSzT_T6nAxZwEYOX2x8XoTsJ0DH-9nKPgdF6PbfSDHVmHTb7IztPbK6jbs_upBDDpvNUlNn_BYfzx3XNqVZ1n8ecEev22R7siQkpsxtqVPDKBDAo1xuPeoyQ4Jq5Sgb3qbakiJCu8V13PvPDmFETr9BLUxX5mGSAr3OVzkxil1sEGuS-mNW442GzKe4HwcZO_PzOiQLZ3_hnteTZtnhgwPcDFHQh1aXlCkqf8sU6q-rxBs0Gr8kinayj14p-ni8yiuzu0BcMDilpAnmPivyItEoIsM8uHdpoRfy2y1eqydg7H8sfyARXr_xH1lK_3gqmyuFgDH4o5dNHMv2FCxITz3_WTXdBCJGjJ24kurEmz-VMyIrq5mxcY6iI2EH7N2EoHUCkTFJm_sNymhNPKT4rGRzah0ny1-3Hqm5pJ02rWm5IQpK76ruvcUY6lBck7ywSQnoTGq02sV3isLg_PRW8IIjzKHM5wzRVDyFi2ItA7CDTYvvgEANtLGS5fURFwyaXTMAr-08WmRdv0o3PHeVpzw1fLnGFCmt8RxYwwCUVasHJGZn2c1joLZcOJedk9Bei5sTxwSvY-9ddVAA_obRN9-yMOixeY0q9dePgcgQN3S5ET0gV-rXbMLiu89WKKze3gEs3JT5pkJktAqeITgAGs8b-8-uQEe1IBGFcz39mHIYNzfJ-BN_7EEmY5bHvIS3d2s7VLXs1kK0BD9_P9C9PMYFO5MlLDx4W00PE6K8gxPyn8CNIOYzNRdWD_bQQ1uTPoQjT-zvQSki9UkmfVEEHh8L5PQBHL3WVhJ3hDViwpYTYrDlRfgh5_NQxwvyCRBGBjfsky1EwD7tOXHPTeA0ZCpk45z-0NOjCumprsmuu5NaQb3r_yY&prev=RQ6C3FDE4821551D&p=16&pg=106)

* 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=rchD82TDzVApi5_PYBcIIwJGFm5S1nmW4N7BywCTSymlXAFpt8r4KbJArP184_vWR80COV-2BnKJH74ueXnLHPsgN7553-xW1wBPqAS5U-9BUBEXmB0AumZXYclHRhx7hHA-7AWYeHDIRj3IzptFLr28vLDj2wk3freCnqglDgX77r8vduuUuojRFWW8XtxPO-EyT9gs1VsXMj-Uco-AYGUxVOfHHhrH2TEQa5W6EPZaGWvg4U9OLJtXzRxzWypXx9pDO6AkKc2Oj4NFuhOSF7DdbRP9xunGs8V7EgOXxHccPQtGE_xSnWak3tUfqOsA8C2_ZWAJdBepjn6w-WJHv9OEzkCyo0Rb3rNt5ZHI7m0KejRYlhjryfumWDO_fkdDPKmS6qWJtEp-t7aABFxMdbuXzncnreTpU4hCvon51cMFhnLaD0dzhwv6t7fa5a8QR0_WBIOU4xy4aGS1KdjGEiehTMrd6nNW7qPRDAUbNLTclo7LXgFxOhB9M4FS43yoLvH4tONVf1LGJZkKIrlZLKTM3YZMQ8VF-xCvHFwkayKQebp_lybUf3IW4BEob8BxJsFtdX799WPpqo0bhGWHpECB7ttu4YLAhhvjSD2t3_DtvM3JnH6ITtvewipB1IMcGMX1Oo87sAjYElmb947aSazv_RLatUGhfYrXUMDC9AwJAn_LH26j2bA8wNISpj9kthZPVHbvyrL2L06C7_PhPihcgcNPXfGdoEODOMB66B3qm-09muxbqAFxEofkV6-RiZFQ5lt8fRxdOwqhJfPowaKviVBqQTECyh0NsGzpMy04_vFd7uWv5IrNYPVGIRdohm5hp8QOdF3eNbBqYvOoeGWx50vo3jknAvOKqDgvlZGnb1alPeMD78eCIzpiaq0RIJ7frHxnGeaMvei5iDG9UiV4Qk9JX7sX6wO6-5sVFzVnr4m1EyK9eKIzv0YMvvmhY0EMk-LVMyWrGX3FfsQJ5u8BrhBh6kLj_cywQ14Vj6UurQK_O5_OAPW5srTUrNuGSiA7adOxWMF_qsmugk3BooqnkNJ0aVQpeI_fGJFwsqHhGSS-pYq6M85lAioiATScdB7cGFNZSaQOry-GurOCmAgOj29GimZQgUWxVOGyEQ13OkG6PrBec4JWIq0d57CWSS3LQVI-mg2Y2_BgKtKJx-ZYecVC9oB8Sd6fWYGApOnmxhi_uP9--f0T1zaa9QTcI_dyBVZf0uspRxILh1lJOE4euDlDRej7amSI5o5sZUIDXYXMckV4oOQV3eNjpcUNi4MhupK-KR6XwZ1JDPTpvH3cB3avkkmpZnabEe9SGtRWvl_MVxSRfdJciTESt3whmd9wt8M0YW1zNjvNlHNo0tZ0SLiQNQhV3rOK4oOF9VquItnoCGNvKx0JMDeCZH5tDIcA2C57NE7KY-re9sbHNTIzg_f4iikBcyGJRi6ZaM47bgIlvwCnTahfXh2WSwNZEy6nJiL09IS586l7pveJUA&prev=RQ6C3FDE4821551D&p=17&pg=106)

* 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=2qyYK_oMCsaMOF9F_Lyu5JBVlr-5qLr4dA_3uRb8IivEa_B1AMM01r8idpvUDjgOmMwFFScQX6cPfHA47kr1dWXraBH4IFQ6W2vWa9SL_hI-du7tD4l8kisOc2344RdTvtGy462-0503nP7VJ_4pLcDEUu64uOpbefAjMaCZZnHvOpR8R31B8aj59mfhWGUSAUUmFx0wwmPD3cuQa-FwcudvrMJzCZJKPFk2pxuQ-p2iBPy3rhCEN4X0Uhr8hfm5ZNafRiTm65uFdoBRPB_rofVSNmGHg4Ca-psk2c0Mi-UyDJzWnzn0SsXK08k00P1FZjzn1ULZ22IGwnGCm3m5YxvWL-7i594LC0Kd9KWZj2Q5lTOCkne7ZgUeApKmGTnXrMghC_oXkYgnAtaaGqPKLzK87LUQrBGHNmIsV67gDu2iMk1t1oInAhVMQAmbSHzeB_fBOmyucsZ3M-byLUfx2JqxeVUvAb3xslzqpQNfXW05Q7Iqw-40UpmxHpU8Czk-iEVwI7tZbPOG4Aubkx1eCpFld4bPBT9Xv3FSQi-huDDLnBFNg8QAnyn6jB40w99hndh2kjKlG2CcyMG97ZLa3HegPn7j4_f5z4zGIwg5guyN7vCIHjkcJXSuLF0Ut__4RhlB6NRSpg_PfVsOrsp_HE-DLhO2thnBkEo4eBHyR9stYETHo76SkeD7tmXVwp_ctgBgLcN6XhcmNo5PNqru_LCE027D2-74oPpndfdv1crcnnYVCw3oxuoGmHcvIWi3L8Zbc8RwODp9GrYg3JdOK-OosFI9bZuQm_rPR9Nh5HBc1mOw62NkpJOM5Ykg77PQ-jBIccSzjcVG1kMYdi_3C7pxjH9SYyW6Vw2IwSPmdxk2CNBwpvTzQGIwu1A0IHWbsFKmwEjhC5EzAAnFb4Epd2_kpd-KChbKsMk6lCpKkExwb3O4JPkEnRqNvQvdwg3z65lH8e_5TsdOUJP0WYCeVMcCEjrRZVyzXet3jISID6-MgNZPHR5q5JEf0Lsj456mnK7WMCbR_9MxNBrojR9Yzkj-gDD6KEbg67m6oon9T1WFx4mFWHi4ACO3IIZrmbIFN1C1apRypqB8vSWa0faQ05_aOyaI4hUFmkZ7C8m51FJHEqM5R-eH6cRypPNGfkiKux23HDaw4VIpBc2jhS5eiMAiXK04KAcy2H6SdnSa8AZ4lcbnynYICSQ_YFfDUm6avcZji6yrKApYzvuxe0mEavIYsDW6H3y7dMR1azddKhnMT1yjAhQoDItiyA7PuCTRwynRhvpGid3KUtGEbjMxTBsTXSpGhSMgSie6X-61MWrYlW3yZ1jHP6lekH28fSEvLpXFn5j0NX-mTRrqZhvO3IN-VvthywJG9Twc5VlZcDgtr9FEle2XKG0YTfiKB-GbRE8MqgCkclSaJifpI745pN5ODSq14wDZdWBY3AVwqfCwOQi8WM6xgPN_zLDNNDD-Rf3hlPXyew1Fj8sgzGivT5c&prev=RQ6C3FDE4821551D&p=18&pg=106)

* 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=bUZ-9gCCctgP3MSfe8MKsT-tMf82YoSZSlucWYztXs4O0RQSUvGpSyRRTyHRxS2noVxW6f0aWl-Yot4oA_v9jNgVA1UP-eIj-bBmwOgl2wpTQHm6sWjzsw4QjXsCfwMMgkmu3r4j47csOCNdy59Aqbm_flG5B3ZDvrm6NcqU1FceIfwnb5kUsJa7wAN5AANEy8YvXI0Jt7mFfRaORqCu_r_TpYbxoAmU-qewAqkRcbRFqGZ4PvWbAMIUk5ndQxlFGPAGFzXcFgB4IWCHhNoEW1aOYvO6n5DxGstVn0N-CiBAX1rC2yOvyXbe0dplq5QZuIIubZSqG87GuEyaneV2kBkjdwoyqOvsIxkWi5avJY19qAsko4i1o5jER-SqtuniuMa703GMVLJTCmgfW4xlLjZD9lcKPMdaj2S-ljjOpg5oD-wXCnL9TRWOeSreL_iJrATElunu-86saJGnM5pPAry2sk0hoTn_gdJJpPbnw6yGdgoVpvqeiGIVOjkaKQ_x5U0koLrZqaWZXcma_zDBp0ZvC2U-Cy3wQ-fcPZdO20XI7JNADycqg8EOqIl_loSLQyy7RHBeYdO5Rs5hQLDFvFSXyNPeUUtRybaj6jrICDnrTuJu9HkAI2HmwyQRySVAshK_OiCwzZpSTsB3x9728dT8UdkRj7OhsoS97rhMBCduunYsrzYykGlTVsMBMgZzUJfXFCvt_eCycK_n7MC_V-sVvK0BJSLKtdUaw-CTTbLVCMePXa9p_X38xZNTlOQ_c5O9p-NYqEx1j04zLdFd0DG65VQMcv0OCNKZ1xgshnxeutTfYJ5-oFyTfhe-vvLiRNeU4p0h5wW67JC-CbF1yZWlNuGR_r2NsO0UrJ6krJvpL4hq6z10AZQxqThn-J6v5teZpAgCmr5Pd-putAX7Mt1EbO6d_QUiZ0PFPFUV_8lNw_zY1MgM4T21XyjTd0isVR_MS_T78_AYR8d4hI-OGqYXmadAYIurEC8OWjZpwGVi79lV-L3866OOKi7v4rEE-A49Uiu9lLXPi03wwyielIDVuG5ppDFxRPabruD8gNrXtA_LAhxgb7VyHqOMuUk1QQ_Jf7IiR1jbbZ3amtTngepfNqYxBtwzKnT4uUoHTInRTPje1mK0zzhmk7ja6x8OPoD077k6jc95QWz8p3UIXUA5DeuqR4JkYmbkZ8OvCn1GDhJ3yb0M290PMkBqZ3TI7Fr9RqeWlPY_E9z6qcLO840kHTYv_hdsbJmGSLMQ7X6llgldYbp4KwfX2HjanvkCEA6AJUZvjzRT5o9UAA5DM060E3jQdS4dJlZ37FgWsSp6Zm5DA2_p4kzevnQzT5WuI84slJWRxXLQdnzfJOpYRpKuoHpl1uRlB6xhUP5W3zigZQETPgg6GyAOnOLDGjhKyx15uNYNMIBArNqiNyYnP7AA6qILOt1y8plPxmSdOKRBqxT0hTCo9pUv5PMxntSIitqpDy6kJ8XcZUvQ7Feq&prev=RQ6C3FDE4821551D&p=19&pg=106)

* 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=lUj5jAW29PBMflV4UMSffJMZQsIfYW4x6Zw3sTtMfgW97xAtcE92UOeuJ9CGzWOpi0xU3RWSCWUD7hSCmrrai-sjBgm_vFJ1D4UWwoMTrCKDt8g-OHPu8TBjgm9DgGenx-juP4ARJ8u0izQQ5h-qiEApIuXG8rlIZ-NEdOOuMzz0A1qIk_CUUDtydXk74Rp-T6TAOxO3ipiq1jOQSa-eS43IiAfQmwGlIgh3Fy9c-UFTQfSh7l34SW7yla1OzDlr9kdjy_vg9mHZIfaWPKF06qz6SfQCB2_21Pp8o-nMQTvsnyXcb7mJt7J04pfN7_M7DceQNb7JF5PEdcPmcM5SUT-Ooc6xevWrS9bLBfPx_afTdNxgtF9pGL9TUzaYkuz0mep6eK7JVWs31ZHYCQiNCBrSqjRPQ9GIItvK65JRvOJf1rSC5Hz9n3uNDv8HbpxkVOMtiN2T2z5q6DDxA9PLCpTcya_EUDNtV3aGBieWRxmvucQdOGDe9HUUQCd0U5KLL-wmQG-QxmLC7CRq_fGFpVQhmhSNVSZWoGe8Z6UKhNzhVjZpKTdlG0YflQryy7QfiicznJgFkhWSwYV1qjiht6VBTdtEewlH2ooC1kwn9XRX9q_RGHmbZGfHJUc_XtdJHRsmN4YUcLe2_JDQz_-jZf9Vq82_kgiOtWyGYn_ZsKwcX5hYfC-QXmdXk9Emc0JGUJUWcaLy2dFfHVrUxzK1yXDa2PHCIIHQEIFlleE7Qg7LC4bVV0LBgUaLyJLmbpldlSZxIR__AUTaqhKzRsmK8F_8bVybVrJQlJ0tBX8s1uM67vw4IlC9nDa2SYEK1j13wRkVEMHkwvX5i7cglHr1GdWQZ7coy_hIZ6UO-4XmRvUs0fsDmaKd4Xtcfe5ETbhv43AcC7XpPQfzdIg6563Wr6vKU1Kw8sCIg1YYHgPPqcvf2NbIWBXO232V1ZxnE4vZtu43DMYCAuqwYA5asa1pFAYMH5q6G2DOIyUJhgnCgqw-ItRf-GFt1suCQ3_AeU8b_PLiUuubu65Qwxy4YlS1OAN1FOt9u-09k_MXgOEpS3w4lMfToEhVq43OULscrmwyRPoOJHcrkviLske5fHTN8cdOfX3117Et_20Jnl5bjtTVxBmJ0NoR2on1lt-hvqUCt9Z3D9i75TOCHnwprYildDgBPOGXAvQeDestvw1KSmhLUZBETFjSHX7R0TIgOlbgGsAcBkkDnl8HHk7f-t50nrTNUUdj74NMQLQwCh3JTUJ3SRX3iHq6rnZlq1Smtm8S20VmFIbDlYZKdmHcaG_KANaRMeQhXFzwSkx1rFeSwRpZqML8Ximo8hmAhlfrhL4e39Hta97BO9XNKliMGLqyukL04ioOhMCLjCLZqVIbPbaomxH_DPOSOZi-YzS1c5oFvvaIltFtJwl5lgJHkAJpieJE_-EX31oXfg9rgOBpr963HYm3gesbH04Tp3bMxrD6rmhiqDsOTQB6Uo641MVlRqs&prev=RQ6C3FDE4821551D&p=20&pg=106)

* 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

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