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# 8854 English-speaking jobs in Italy

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[### Clinical Research Associate](/clickout/f3573b8893e02352?ql=l&sig=9582c1068c1116cbbd9e624923651116c79db8ee&e=LDnkd9IjjdGG_bHuETMSz4B8ytGOTTW1eFrRKz4PDQURXUtRBKY9e0wHywLkPvaeiSw5qxQjGOsmgJy8T725NV9ZxAezA7Q-mRXhEldURwqqLjlQQ0B55dT4TVAkS60G74vhSrQ7EANjXyxmr8LgVJY7YXNaxoM1i5KNK3F9SHEDuyag-cNvqajHQKIKpyAQhHBLKq5xoGg8J00ozfjdpxj4_ax6ATjsLGBc84krYaN6fX1MFtiRyFLU6UqZtvyYNof3OuL1mlNgBie71yTVRZKx6YeoxmslnNhSU9JrNqjlpuBOYBMU1GomwBQoT4mXEQ6wFm5LhHCFB1-KraY00XSfnxr3X94y3pLMLkm6wljV5NeNHjxizKfq4HpVYvd20wXaETwee0p3oArP-UC-yQRrrn0VWDpZH9dOwG3ONS9rYRjH2k19Lg9LlxTdGwXILCO-7NWJ0e94Heb5gndOJM-CAyPB76_ErZiJ0h60931pSdgyoFP2zR-3B4KYsVVn-9IT-wtE7SNOi2IQRCy49pbeNalc4UKFJJ8AWTzhAZI-z2satA-9KzweGwzN8bFY1JrlIQAXvTuzm7StaGiwnhXsiJNXWcjWYvpqFyo52lm_gYqwHrCc9skOLpT2DEby3PMa73lUG6u0lWHMRskfN8WHU0xERpJUwCAvwdu-KkgtOUt5d90BfIE9WSBBsGKptQaatuW6aQhdrLsw5LZzQ6IJJYpCv976LBEmYFvv8yQQSCevvPkTaUlg_1cVrcKu9FjMt4Qa91Z9oWwMX7XrahxLrdUxL5EIjKP37t5jkSAdoqgu0Mg_hTFBeeE9kxr0x9Jn2OgX4ZNxXVJwy-fNIu30gm07wafVu1EF6EwIGttkzYklzO4deVxL23rERLHblTKx8LS44sBntUHozw6TJuETfLZaUbqOInK4as8RE4fV76sUyz6xXVLgh6zcWTWaqz2dbf7x7GhZo9UgGIxBnaay3utsBV1u6kdxyVZXo6wRGprKULlSlv9CAdJ2wYXTurSqB9LLBC0ii8mGgbWcgtJvvjLuqQ5IgQ6Jl8fML1Ze4kJLLCYafmX6hGQ7_m6k5GD4znNrYDazUBIufHA1FnzA1nw5RJmz4y9Y_V6KS7NHcZpvjOg4nJXiDQp7rS-8Gl-ElOJuch6gTjeMJr4TngC_fYH02YGfqU5rosDzuuf_hoUhllnc07e9iFOtICZ6mGF--TaNvxqln_LG9vnpFHeuPeVyTxZjGiPlnBipB4hJwZ0Dc_GtiuLyCpKQP-OZ2RPAjLnfXFkM23w7HRr7ccSE8UPXvdPWMKT8qyVystUmlijX-l8H-Mwx4rROex6HKFWmDELaTaYfKIiR0Mqck1a66at9mYb2FfuboAztrUBdysP0bXe3z2ATv3k1iWIm3lcZ4EdUv9RAWNERew5gN7PVPPWuyS1RMotkGNyeg6hFS9xdLp9rjXiBhmYro1qXT3aIB8baTM2DcxqDwjnNLjbHFu4sKJEk&prev=RQ126CCE79F5F2ED&p=1&pg=105)

* Italy
* IQVIA
* Reggio Emilia
* 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/576d957cc201c38a?ql=l&sig=e87c7d84d9ac1c1185e727e9ec60e5c5101c3960&e=8uiNVOPJZ4p25xKrO32VSEDErPwmAgUC6xgU2SFnIaTiE-EshK1xxEgxUtqrrVUArwM_nPFupfgbVjoVrBXtb5Keva6bInbA6kA-C5Ya-REcAeQTcj9Dr807InQIXsuEdR-4JjnoXjV9kCADAyhZYDL4ARQEstF-PECTXnThgmYYlMVZ5vFWIYQEt-KV5lUwriyyfm1CdAvhn-QaPIsk8xZopQEqijCPISfkZ24FfRy_AgAcebBaZDXxtuA-H93rUM2XhFI-Sp9TPStPr5ATzQomPqEUZv2LZ7-2H_iWBeFcVOwLcTCoYsXQzoCb_ppzKBNGKHP5T83EuRpXwDNl5m1ueiTTh3CbhTU49hg7UAF4gxmrDD971ZltY7zUQ5SXBZdxBfDeZ9nT9PkAEeU0ij8hzkoCdbeJl0IKy8AnvE5zGROPmQC8rkGJJUbuYkTr9-M2bffOQwZi84lbdBqevnTneQp5XUG0QD6Vce0sBj9wUSR7yL5cAqqMbIgd9K0a05oEXkwI46CoSdmxEAfVwkrV_D9KX-MnwnCmZgsdf-hmFvA0VzM0LS3CnaauvJGtYOmqNdp9-3YZ6-Qwgmxab3Iqq803TOd93z-8TOAiZkg1C2VJrWXHdEQMRxx55grsfYMvIRxXKhkPb3im6FoQvyY5Q3eszmsUttGKTAvWN9X3ExykgUw1kza-W4isf9YfiFQpuFSf-pVBLq3a3q_l3LZUSUTAoUUnvgtSO50lxn2w-mGNx3ivNpmwv2_TngDw-4njWHXc64MOhzzc1gJZVy6QIOGiamDV-aLyzLpGtCpUdB7rgdnG5-9CEA4dJwJ3M_yvQxrUtSpj3QWNy1-kr37RKHJTefY_CWDeELAIbx5b23_w2NQ85_3lKseLrrkJnp6iR-GNYrx608_HXFC30EgKoF9Lk5M2MHOStJJcTgZiuSPWMi2bfg449UlJ3H__1FajZX-RIf2uw92BzFqKXKQVca4YlxSO8k41LN3X3LpVuFDCzRbGA3MK4dFNW2HeZvam6FQIJfDwyMqIiz_1wkzhjU0yhM37yQ6nYgwyY6PzQzNE66jkFpSb_XpvRJwIhvRasFiuP7RHpmJOE1d5iX6eSJum72APmgGMRPKrR9RC9Ldjm6AesOZdH_b_fV4ZqQwY1JXx28o4H56hxC3r4BoIbH0y9u2SivpUZtg_j9l7t-saZuUzno3tAGOKGON9F2O11iSrcTwvZ3AhM3A2Kn0_ht2UPsCOxUdmqMyA1h9f2e02FtCF2oGGlozqAaSEKFyMQVkMZQC7kyKbG1YfgKtyubxVqio3RS4cuLnyRcT9gIIjmidE4YhsubDl4rj2K3QuHJBo6H3hJ--3pV59ML4653O9pzv7kqBYXb4MIUTr1VZLq0iuTM91fXHwX3BiWb-4eA6d4bVRxgDwI2dy4pB2ijk9ZIsLhxJGPgt7i1gp_GUQsqo_K7d9RROly3Wgki6JyB_mdLfa06j988DU&prev=RQ126CCE79F5F2ED&p=2&pg=105)

* Italy
* IQVIA
* Bari
* 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/f239956dbe519c68?ql=l&sig=b62c854de9ec1b4f9109bd9709a48d7adab2c153&e=_I0BpH6k-GnzMpN8M0IpxuVCjmn_NKmoCwaWbmnIvFujWx8eyKK_mrIhnZOjFbgS8zl1FLl66wpeZUCjECmOZLpkGAfuUxKEyJcVUYjXj_k1ZArIqUaKZoC2hBijPjr8PmeU2dwPefxiqHv6sVwKk_Y_oJRkxUYzyewlqzuWZpKXPss0JmnVxRA-Xvx1ntGJTtzxakKMLBqEBQTczDofE2GBptHObTE-FoE9He_MFIrx1badywPKxsD0r5vOZZDBFXnyk_dacAT0434qa5mIa9mvsmF1X0KDrM-QKw2pl4ARDXWiLdUX1A6T9oMruzym2tNJ9vAKHpIUxg6bm3rs6xuF071MIEcOz_61KtTcgdDjVn4PhhogwUP4qt1sM1phHgUUtkeBYFI1oWvOfUKZoqcUia7540BHkLCFZtpmW1HR7xvvJ5k1KqGr_iCgUz2RSFv-XmFn39UQMI00ZMCWGLxG005QYLea_ZCZTRuDLo5I6WtroFr03NR-77YfrohqBt-s-csRJyzTSxo89SpO7gH0g9IorQt9glY3Zx2A620_oZMdHl0bLohatTBdClqBCIwov3NMdYwGiSptCEWSaUBlKP6CfNqSbhLXrElEO3ESd6IlFWXSQkruVd8GwnJ8WVCyxbWwut7L8uD1RB5kpVvwDek0xU_3XneHIX569NR7BxsomvIAA1WxfA8jX-ledgKMWu5l0NyDYPk4HGs9-xPTFeJpDA2FVy33Pv3FIY-8vdR8aqs6MvAshIOUJwDWJczbFaDCVwGhDuJUPxKfrM4Js49w7EuDhYPLT1ESYSOQj5Smqz2dGuG7mGKF0HwnFylqqKpnffwUxyoenG_z2O6stnCALG0wTgosNJr5sO6LML1DZ2QImn8hiqBEMxWPhOJylHdVX_qTNsYcWLyuweJD5CNSxdbIYchJ3WeMvyGhHX8BfOc5yE1kyFAnI20H48Yyj63UvS2d-Nqiz49lfpeF3NozDLizZsJc0bmHy5CmWIQsOKUI_bWuyV7_fppw2weC7xCEE4Ua-iKbv5jceMMEtXKWpZIBjP3EjNSKSvL68hvjEp0TCyxHkUar7UBJXGKgvu180egCStJzhAyZROmhYS2aVJsNDLsdl5XeIGJj-YtXVm_ZMW4GOSqmvKhZCGvJXOmkrHdTNDrI-_wrh7dc6eE5Z2EXU6ennA2eWa-L3yRXS5rdO1w-reFa4ive6dFtYmlnla4iH57_ixgySgiFNVloxEg61batKtXusVLZgzroDZsEB-EfuerLLxOsS5niB0HxsJQP4FnhkEs9QrERFCez1zETL6GeCYG-6V669LmWw0tcSefAkQeiwzGieDDtXpwr4m8umAFuL-2NFm5PlVOKB7wyICna2b71E3jWCbSEVRKyV1e8bLZoSe1IAxfL72i4S1uYSGu8L-lvTb4R5TOkLAFXjnNQ-bdI7uqqKM2T9uh40gPU098banFNN3GCHWGm8Be1EOGTy-0VYQ&prev=RQ126CCE79F5F2ED&p=3&pg=105)

* Italy
* IQVIA
* Udine
* 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/ee67a3fb96b875ad?ql=l&sig=1a0e9677402e35050fb491b286f8be1b76e18ac7&e=mHEhi592tZgY-tlgDXyn23lNxQEirHEzEppLsMZrQge3GDFAnp3KzTSzgKWY0JWpB_d2WsfB7EnkvXQZGyMn1_eCY7bSzrrWdgZ39JGCyJOb9a60ZQBtwC1j-I-UB69jiELvkSrPNUKWBYv2ZUqNLmTw7iJ_IOoXnAobchmYogdJxBwzbv_GeqCM_h8mgixviDOf3XAcIiv51YGkwYhPLJQzys2RUiPvQupZRckJSTYxHjNnjUGm7EJH48Uy8sLJmZYeQAXqjN_Nt_Vn3EeyHpCin1KTMxheoJitpZNUEp8WrTvwtGiIBCOowPet8L8-xDNJEmjL72Fdu-9VjZIZx-dIW9A-x4auwNo8Gdx0pzfvmg79IRguYay7YCjSPxaxd-sEu1l2FZFVLKrt47KB07s_og9VKg-75WlrgqjNSEwz4yr2ZO0n-qYj50jcq_qk9MC80gjVLTI6_IzpnCKvTMMcrZzMEhZKSNbPFMb3E8ONx7IqYsWoS5tcBggG55209gshddaTMcEL_EXS11DUd011jLlbyVYBGTNKarsk5orTaN_mSDdo4PfG-3ERET_cSEXImijoVAoYsPtA1CVGXxJn5JSouz0E0Wdu2K9tiq6sq_xZvbg5CVRY3g_F0vW2YxTYkLguekeISLBP78H_qTMBJPaIMGq5pfY0tEEnkqCDvBwqzmmx3wUtb5QRWizI_aTYTKQuVaDOZL4zylvUF8KcEKOlTglSD6f_5QVrPaUWhto_mGGxubeIbKZS0BR986onvm5xtAXNqfEXuuJrkL0thEyq5NKYeNYu6d4LqKzsd4PBB8ORVSF08W0kfloIPatLVIlEMfBcCaY-pv-nJa1E4HgQF7eDKaMdvPGoIZ_Uqfk1BytM56Um8uOuDy28xJq191BAUeGStXBRXMm_bVtXhPIRK70MW-kM6du--yCO1ZYBbx8jnBZw6nRV6LBcbg1BaZqXxXC-DjzHM5HpDd4MHP1g9TTIfy8Wm39A2TJzZQ83qIi7v5dceRg9TVu9CLHH2yihWimTuWAVI-s01QW-1EF3LOR5So9eY2pqbTgqh5_FmZufND4Kv4PNlWf98sVmvmlHwAgGQ9gCQ_1dSXEGsYcn9lKlgXCaOdfOkswdRjhkQq1_-hy88IzX4XIYcLVJlWC7nVHx9sjgwkfsWq9Sl-LBkpZEKRqxWKnboABDdFVKGxtqK-0GBTVfDedpZF1z9y6Dscs5rKjUyWnFGvxTdXjnjBBOT-DS878KD-TFbJxcZJ3qb9QFP5n7n5p83ZApJ5I8ZmlGkuWmH2Hd-Yizefa5i5FW_sBZLekwa9ot63KJjJM598XBDMkbfEOfUXuOBrmajQ7wYNi7hMBiixlXbm9UoKAHMybg1dEIlwCn6VI8bOMBTpyhIHhIwVvy6z9EgnH25ZvDO9rYZHBE1vAEShXpxrbKGmBC9oTTwFN6mTSKvkhk9QjB2y4nzuAkfUcKP2HASZkbX54xoz5D1A&prev=RQ126CCE79F5F2ED&p=4&pg=105)

* Italy
* IQVIA
* Monza
* 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/669a7dc5b45b143d?ql=l&sig=d654abcb2ac0cf369b61bd78ba2b7ca9e7d72475&e=HD-rTUgp4KGTsDYFkRWv6Jj9rMmim-0D6qaBQvhZ17GOxP3Wl7dbBFL05UIvloUtZP1jvW_hrczYBvbha2Zczvx9jKhgSG_WXyb3X6UyIsH6eK--qTzEWejvJPezzaIdSNnJ5dyU5DryVawG_P_NVqG5iAwK6TAZl1iPe06sjEuOtFMf7RcBL_RAjz3zO0HFuwK86ctmJvofI7xeFx1j1eHk8H3_qqOp3qncYnTu1MhsOaB2rkeBrXodPpCslTCWlsRbMTnDWjlczdXV5mvzSQMMQ2ges9hxOErJgJXvQHEfLur6nsTauiYXdTHKW0QqYnC0XpcyBbh7PulRzyEljLyHBeGFtfpELgF_2XvFmMI0yZVOpjyzJyy4V8T67bMEL3k15OB3Cgm-7CFzmjp1xVMiktjG1zFI9uazAR3tLUykc79a4JTm7-MmuEyeMAzeZHbfinza01C1RrXXHVicyeTQmi6VRd42CQpYVaGKH4tEkyIrkc-3BpyEntU2DR4ZwpxyHXR4ic8cDAFeReadCxe260Gbo0B1_8FQwbKfmaJ1k_bzhvu9F30B0lU8CvTXaIb9DR9q7pfU-mr3WMDbv0OghaGAdYhXhirix_Bxk7uOW3EK6ewKtfhqsV_1tkoMkC2DekUgY3tHDAMJBOSD6MEQ6cAa0-dnvkts29u_iyGMqQmvDE2Rw0xplahwozoqKp9LGCJ3-Jky9KYFbTfZwtfMm20ej1pNSo2hPbYQB1t9y9clVVKxCVY_JybOBk2n814CyymhI5IIzOTWa9lfQ-Kr2wXk65WPPDGLAZUy86hwXW7m-VGvWrn1wBpJXDA00sPfox7qb9lEujkknF7_npShOHJM3_LAb-k_LzOZHYGUP4HkgB9kpWnf447XrmijXzAYNJudA0ZEFYJrzi_TYPHyWSU1tQnQKRJGuVhSpoF8rATwA3v90aDuYxdr1dva8eRD0yw7_NC32pmFm1Mb7g4CAVHzOlaQaFmZ0Gf6yhse_X70uvctRFhkDZJh4T8Jxhb_pjwLC8C_XpTo5EoFsIkSxGy5ZL_6nItHhiV5rn4cy_i04XufcoycDeRxDLwmJo-zB7rQ7cpftbdbaqA_VHmwHyE2nVi6Oms_0SfpKMqiAJVta6ptWKo3YO13GF3ZYIyPx4JyLF3hGanuIE5rHj3LYvarkd6pyruz2esWCmnjYUaANLCVCDczOE8Eqwio_tL2avZZCJQtXEo1DJXTZcwp2gk68BkutrBisXgn-thwKFcRtUqcezq0mMevrZKXpKQURFcXvDi_ZYVeJjBAeGOL_KzfdFvp6tERNiA1v2BLLBonMsYPmZ0iaDYw_gtb107SfabMqt-KCLjhx-wBc1K314Mkiv2z_l7Xsd6Bp77-gPx_XZGldKUDZDiJ8ac4xHGeHnmP5u95SGH_mZ8FAHaitvkHKHZxw1OzNB2eLoRTMVAMHDRdChgVbd-7We5QDLogZcR8KdqGLKWy0Z3ShVnr&prev=RQ126CCE79F5F2ED&p=5&pg=105)

* Italy
* IQVIA
* Bolzano
* 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/82ee42d7f16c4105?ql=l&sig=4ea0bed601495c0a8bb628df09add5d43281b861&e=t83SOpWL-_2ANb6HqXWTXsy-iE41TgXzjoubhA3KLe34kUkNq1VVLoVero9UpTb4PH_NmsFIYVsU_GG4PqFXZibqtr5DsHYvGklA3UkXhFPaTZgokVnDWJSzZGQEiNure1tFqaPuCP-W8sIOJM13C9NoiM1ngtL4auFhWVvuCtgnfr36dWv2aG37qXg_OzUoxdNwNcQLc2uYBkYx97reIDocz8e8GWwsh56TRJiFY7bxcVplR8tUfidyfMu9bbwBnHDRezsjq6mRATIZv7bNUf2DNtMZAXYjUCp-f7WFkjfaFzwoo0JIYRV2wgrpGKjL72YQZb1I_iSnTcaVpH-98KEXN8d5cMfzxkP8tOE56FdYG2b62u8TH2IWn6vGRHz-mUUHh4mdNg6_qyinyEgwezyb8pOOmrEACgtV5wkZ2w7lCCN-6uLTn4MzqYerndxJVgBgKA7IjItkxKdTlGMM1edh_EwgvxsmXzC943QXI30HsaLKM6u0xh7Xomw1FCs037e3boqBgwkGMDtoPG4nfn5DQlvvj7W7gzF5oNfr5-lJuZdUzbnfFDBZO1PZMTgME7-1e2iFTKfBCazGRXoRxWeTpDOaJ2jwL9WNcik9WnQSh0L1d_RcCJo7i0lnz3Pnmi0o_WXiluYBarCQWn1-Q0xWbvQl0E6oamIyAJFFlBTaUilbAQ8-89P8M5H3ekkW9K3EVPU3ABWxQOaqLhrMZoZV5PPTDYQVci_-p9QPNrgOrglriDUM9zz1UZx8hTFRxG9OxHuhaAnh1NBX8Ywpiu-X7we78nSxSRgNMiZHtu4x6hm5EHO4NRGJL_pXsaJtNz53MsapKJ3uVsMk-s1ZAAfPyfA5WaVYmce8mowBOtsYDDvDBUCrqwOmZjYcUaSIfZBTRGhGHxWakwLHeuKppijTtB5vE5Vs0RpthQ5B3H1uw7iwsXhV_EOEkA15hY5KSEcUH6pDau79P1lIFQTuSXTtBR9k8grIYdle9gALU8BmZHvFnLX91detD6MM1kprBaMG399sMFTuH4-tU23q0t6puQ549zq2M-GfcU7DlSuETtwMf7IfoMHCdJGs_CSEo4SiWu74iSmNjlaQlKts9P6PNmfPIwVMx2rj973igeqbny0gHPYedrkRbZG1I6bPfqSkD44EclP_UwOS07H5c1qeMvwBEJQIYYpxLTknrKXpRO6J4Cc9qKEk27sIPPQN6H1KvdTwLBuE_ktWnKI0yCuTds0SP-2CyfSg_W_07fWFttaf2M2IczKrhDkfKRxQlDeTSUPqtxTaOTRL_0_Lc11zxd_Uo0bcGd6pACy8mRSH81F3P4FHTufTpPzAL_eSQ2C6bgFqqsh21i6rBWWy4t2NdXrjdCtiFy3NqGSv5_uO6CAcyZec93jSR-I74ia_zKM8H8f0XgEg-E9-QIcKTCulcKORFz0n6juFtwgTQ9G5L1wYQ3NTbFkzZjsKRqrS5MbKzuVcRLSrJGM4vzqVVEQE&prev=RQ126CCE79F5F2ED&p=6&pg=105)

* Italy
* IQVIA
* Catania
* 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/bcb56da0df885847?ql=l&sig=d8cf817ceecc7e681440b797719cafb4a00aeca3&e=ou3deJD6cjYwIFZt-dgLB4XCC8jrwUHuix_t4BlIEsyzvQN4JENxbxWMqd6XirPYHMEUlAwqn0BCobs6BoEqv9_9GDNIWYwp8-xvQj-fdRLD6zw-E7RUV2Ixhp8cqVgXds-uCMTwxhGV6UrlKoNc0n85d6ap9SBWpJweHcuCR28zvA_qwgU9I3c-3XvFNqL1NZcArsuuDjyNUhd9N_RJMmoyIcOEJMAhjnrBm7Y0VJ5EJ9V3YrQ8zBQa7BrtcvbJh8G31L4PNLdsCIcOG2-_eAt368iqleRkDrsqgdnrNdDpToWX51s6vtKFmF5ITHFbaqc9xlBw_jJQ-1w9KqU51N2rK0QnO7EAe9vvxUKw5Faei4bDkhWT8vUjftPJPuY_2muMEzh_wTUDObsMb5J_P546Jv76aW5mYVgcY7Txq1Ay8Bu2s8KWog8T9jVj8MKWmiWN8FxiwJRzMWpyP1oO5Yr_ExIXm6NLiRHEg_ouoNNSALYzG6-kxkkJNZJmAybEd-M1GwtVv2-P45fLzWQquowNl3forSitXulQG4fcrmCK-Ovep0X1PeklPABK6nIN4PnlLu7tSf435U3QvBN1mF_jY86Jb28ipy3ZeA3xrVdwAyIh-3WxrVZBxQGzyAIJe2HqWJU-MEQ4_vd7sySUai9vcov1Nv44IZlNyGWy_WWzDtvCMJm-frYKZU3kkbHE92T179YT2zIlJjUEX8AjaOnq74xLFx6o-M-twIIqFXRp5Od_jsiSNzRjctxX1SOcmsxbyG38G8HHK3pSKB8JOIkqft-tOVomGkbv7eDANleFvjrUnrsXhmgPvfwIXLeDMSDEUryvFZbxB3uaFknxIz0p0SDz319FT8JYc2XjsCSt7zyqnvCDVjzqYTBI8EX9J9HI86t37_zqg8DXVSodHdzU0_ZMHEulGqu6rh6AiEqWotRzQuKOgENvxvw5tV3941RHMERonjIyZ1XHnG51ciT_Ai2r5a1PFSpPcUoibNZnYpoOsOVwiJc27RIOFF1-CATiiOp1iCuXkYrLVJknlXD2rY6e9ibagVeLdypXIemhgAzC4iqLGjuVOr8of5IN57vMXus3pHFsBo6IkU7zA_gu-o3iurFwWpK3-SPQ-VsKNDVri4OQ9okkeYoTmMu7b8GFlxr9TfdVWohaj5jhlh_w2Z8mptUHOHaDYXv1SJUGZUWvLKT-BhZAOv94KNxYXEe_tsEPSBXE4yjy9TlWB3bDn493V-r0iXxkJoFp7fGX30P0KbOmrifxGVYicviTwO77kt6EvrylnAy_2_rrGWh7iotU2DO-pl6XVxvOJOE70Yoo5mPHXxWzkbnmxrgp9DqeSPz0B2pc6bNkCVRiLZLZ3hP5pO0qa126e0WRpLdd2MLQxYYPId3TrFQBCyM9I-v-NO1DqMpz3eQyQRw86vJ4MCxf_YRRFBo0SvON2-3vRp5yuZEdIeaMzb73oiTq8EJ4VDakhw6sOD8RuyP88dc&prev=RQ126CCE79F5F2ED&p=7&pg=105)

* Italy
* IQVIA
* Trento
* 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/1f6ca4d3db65dca7?ql=l&sig=be521b28aa727e26b86c5a11b06d062752d4e0f8&e=cFkLAn7KDQ4hpTBQQMjWISNnPNpYmOaNxuguMpcKpc1LlxwsXLUSaJVD7ZGxgUYWKO8fm6DMqR0sGXV9zWRWbFo7fso91o290V4qx2QuSVF4XTKFeokF-oVEP1i9lnKqpcoKoCufevXUSwaJsgjnrOtDgJ_5pL6RF1KCZ23X05fblj09Fymdz5sKdpMI9dWhXJK_W8ig-q9S4Xx3jUlKi4IgG5CzNPDC3xLPpoROltkWuIJH8BPwXJB3UxFE8rxBp4lIZI66NX-mJAfjxxwFc4S5zMg8Fw0aWYeOzk2C8tAPLOomlmwyK_XowvFpXscMZAl3oDBagcj1K2QBTYNbW266Bdxh24HVUHVAa_3b462TMmB7bDHHnorU67iw2dNJc3BJf08RH-mQd-noozivl05RCufYWk7JKougc8TEOLDyKCXWuqXKZ0yH3udABowzzVIqyQt8Omd0y77M3Jn2kwoE6u0SOPqzOyXud3r5-Qo2775901mDjEHpCRIr03Ua5NnfPuYHtemvYcl5L0DnskT6rlla2rp2JPLl6za_KDV77DvixG22gT3CfN-XxlkPMywLaQlJnmHtdZBkzc0hTI4qFVFRUXr1ZeugpL6_TIDQbeklJpHkWlnBIob9wYruUKyEKiShcAjWLe1vemJhhW9orcT3gX7X_8q0X9BSyN4kXu-emLy6xgBjsNpyWl7y30YXimW-70oJDvLwBci9w3zI2esvwUu3hdMpYwXDa5n3s2DQq_mocwaEJANeEnDdycSa0anszJIlGHBWfOSNGlsLGfU-PPVvxHfpgxBuPwrrlVLpjfx7ycpZqBPwDnUt8xpzrG4WxVsrkIVVyRFIXgADDRJuc6MeMchu-1Jp2naK-xh4KKj_wVWOVjymrPZyZUdeRQ92H5f1AI_8kuhrWewXo8_lW8G_7_PDTwwayMP-XSwvMqHxCXf-WJIYInOuV6pH1JmXxzHL5VysK4jo2EXNDqGNVXYTyKsXO7etWzv_2NpFsk8PMCBJOoTr0MEMxEY3q-OznD11G6ZCkozf6mhzHNdACuaaRH_N7WArvJsSH2NbmtwWMvEtIKZN5SuCy-KZyGL6NY14JojHrOwj7t9jsW9Iq9w5-MlNyV-dSMStDBnSyiEswKpe_clpM7tlEbNDuKHvolwzmdwg9GZ-T-cOqqc0PMXa7b-QWSyepHypdkK4HqxvuL3Gdr81lqp31CobHeNPjLSo8XliIkfhIBJDwpZMJ_2iN2zdxnIRYXbWNxBnkFFs7sepkMY6VsEmqv0awAKQ-SJNdu7W65qhIZag3vt82Rel8j3RQXsM6wC-5GPg1P9E5GHqae-8i5DsUWzLpsgTzIMocVVmUqigvn0w1rOD5shAgpeIAPc-SlulVoLBpiAvESCMrbRpfNkpJU0ti_qAmmXb9ygDoQw8iqXhqQlfzL1hPyXWZTOoHalZLnz3isfjLsLFHd0QGbdnfCdfAHTE5YmWQI3cSHG9HSQ&prev=RQ126CCE79F5F2ED&p=8&pg=105)

* Italy
* IQVIA
* Mantua
* 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/8bbfa54e7856e97f?ql=l&sig=bd6ce1319a3fae373432ad46a74f428d696edf29&e=iyUMHrJOUwLriumDeI9xAdZ7clbBaKQBqg2AQrmDbYR5PvN-nL5QRX6ErZuZ3lKYa28nNq5PPkKNM-rVd9OWceRHZ9N3SvqGudtK1SOB2e8IuWNOBhJMEy9ljmqFe8uTI_z04qy7ymeciaa1O-uWjD534f2moVJoxbEFnZ_73a9VVtIUqOV-gBizG8CiJjryrAjR6Vo43lPiAEBAzWNpLNPcNJceYM1DpVN9BGa3ExZba_i81PWF6p8tZI9nf4R2pXYGrZAfsdKCZIsQCJ5rbVMrWGdUhuyMXvHqP9TXBdgwWHoK9oFM7auXFviWVYwPUFpRQl8PGIYs4OE2ZMt_EADQPLytMXKhiO3enS--MvkJQnJnevHdlS42bpPOqAUMLitq52HnGIdrk2r-7mGO9IBPj4dvMLKVpM4jMC8x-KIfjTnAlRvzWVBDl7Tmpvinn1mqNEToXdCXSlNVZJX3Fuyg4pUZEKwGlvrNlvig28AcjQ118HGQdooTgQTjNDjgjiGl_yfFHm2u1mUcGyxHxrernga0eHSeyckSkodXUOlSloSJ7_YolQUi8ex8dBW1xinoEncRF5Ak_ypyUIHdVmRvsx6cC2sljTF8woZtWwo5Qks7YWgvY_GeEYm-WbS4yfajUUULdIV_EHsBhDlIf0MSjQybxfIaJJCUAMu3q9Rk7BjRPnRof177Z_2MOLxrJKLGXmQ_2GWC0Nztm1ZLmFeVGi3YMZ5NSXkzI9JESJMGug6U65_0IXSa3F3J3Jzo5VDZdhE7cd-Rz8egwks35Z4rsnPVnLDeMjQBfAZmpUqYpYXJdqY9eFf8wxz0az8hXsRWfXdr7TOPGu40tBnowN_REevnmbpzzGdWX5ncep3b_6ujRcOOlFvhHkJdqjm7VVlQ1o0-pRGYQR4B6wT401ZvPcnIAYB0Y2zOuPmIoyHvsWfFdZgyy_rTrr9mCU3WBsZGZtwU4FzRps8fCWIgBiDIdqPNLGSZ-1IWEh2msYVEcfYg2rARjDSmCHPGsdSwHtjxmDzaLnMXD8xj_8rVSaQ2DBMp6o6Aj9cpP255hrTxPnRKpjywSv8kgneqoEuSc645b7TazgignczR1qjxL-raGsMYYahwhqPoazyVMUZCdcUxE38lnVLErNHuei9v0wVuSQWflff2pqrZKC5ta3HFUPyEAqlOQrulHKyBhU76svAPh3PdhVIY5MDI1_owqyGF15_ZvmP4uZbtYXnizQJswyu3ecjzUB_ubkExCBAczsRhZbeOkweZvyLupnONrRrmYw9EgkR2MsES5IF223f3a0wRh9ivxZlClAGbb5bLp7yRRb--8YpNRtfY17vyl49C9-f6TwF_BBRb6SYXPghaThYlV7rDConX9yvnXBFkDm09NluFoZ0dhzE6vzZbeepgCjBu_8FjDUZCsHL-J4-vXC-y_K1eeTd-K7IzgLJeeM7GIYVU-vFnltJ93MyD-cVc4qTxCAWlCHlJd5Eq2P1Y&prev=RQ126CCE79F5F2ED&p=9&pg=105)

* Italy
* IQVIA
* Ravenna
* 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/21d84269c3521353?ql=l&sig=42dfaaae65b72117280ed1890a3f62a4850adb63&e=OzNntbGNFqODyGLvZ1H0XR2Z2gyli1bzaccGD96gYp7odgT9hwA6NSHFVCz3WZJtb_--O-7MVEQXye2ERDzBeCmtJgw2X8kKKuSQ2wc6T482nrTMjnxM3TMO0KL8Io3oknc8nA_5UHeXivTL6rYf7uP9RQrR7qaSK4cS8dddRjnv5VyoIZtVyfdh8RbJqFlZoCRkh7ErfJq4y0ZwpEGHAw0ChNBKnR7H2pTM7g52IzH7Df4xT_NcneI_m01PzCqk1IbNhHiIz-pzzfz8TcgbhWCw8HXzHpykSh7JLnlqXle6qVxUBAPy_rV6Fd3-CORNMrnI999Q75E1d0I-sPy0E_SQ-BquFcFuZTBc9CdYnGxat2c3MTXL142swOmqPhocxublKYTkkDx24qKCfFH5B_n3Zyy9tQzNvg0FbI5UBmc4mFhDDvKh0JhHQbePadu2d1N-yLj558AsSx4nycUxUmkK0AT3F2h1Iwln2nFZWDyblONzf3Ffg3ub_pMLY6PdqO41UGzhSEVvGkzqmFKOchLO2_TH46sPWQ-PpxvskJRQ92wzBpX0_xA9OXMptdp9EFMb_UrZWe6gjrqQg5fpUfrxFaGvW98fLphtr87KNhKfy5BO0hqtkJ3neJ_wPptHcCOVhpG5f3nDcO1mk84Bp5nkgPIJcrm2MFrgyYafqy23OQV1KZQhOHiG2MVrOL6KGRj-l6zr-HsbGVvdVs65z2U1siVh64SSbyC1yhs1OwOtfXJoZdJaldJ2r2xSzPGiy1jR5DJdIAktb_sPa0Dy2vq2GQzKkL2TK4YRd5tLuH6QMTCWHowAsGncAxZw9YfnkeB9GEtgpniCaMWWvRtjLOmVa-gks2i3ZGmRlkLgr4z3_frrKA5l30qqymVNNEsCuOPgDZQ88Gi9MIt5mJ44-59m2wjD8e6RlCGnsGg2tefAJljL0f7VBZsb9sfvk-P_7DB4sCL7rgRl2fbjRGvMpUjZz5-HgkoDLfx-3oHJcy6I2psFdXvX6mKwT0zmijfXKH12eUz4-CqrliNrgF1ZMSb4gE6rSaZBvpSmPh-beIhj207s2Cd0zNn9-E1sgoSEgmSigKdIcqULD4Icl2KzN6Okk8LglfCxitndm02yVB6Wje0fmJO5IflJuI2i0NzhC0atZBoI48aixV93jiGjQedRwxEne7T7U-FMFBkW-zOPAI-uUTa_aijJ7L8ijEVqDgp-hO0otVfIYoUK3tWOM8qJ67sGM-33boq8Xwlu4v4IwIJP5P329L_mX6QfKPcqyjBiZPQP4BSMTiCepyBtHUU2vg9w9EE_dECq5eyTFZsSm23SiV7uLwITuiX87CZGXUtVKkRJOEEx7XLAwRrrHc1kzViTGeBDPCJr9Ag_X1KOI-wgD1ayWemaJTFDH8uATaCmFRTm9wodwTae0Kb6vUyaHjSJCA_yKtXx2HLwmcsqwaVWozGTRwzbSK6kumHsfVlexBwnFc7CIMHCveeg&prev=RQ126CCE79F5F2ED&p=10&pg=105)

* Italy
* IQVIA
* Como
* 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/15ee28f32aa40b97?ql=l&sig=fd33e1e82dadf07ce62c3b2d8b80462e9739dc32&e=8Kfnyzg2Tg_cpxoqCx91YIiCXtyfJQrZi-c6wCf7vLKPR4k4cbyayaeS-lnNWTlJ9U2npkm_tmZziNk7i0Fb-VE5CtqlJoAtoW4lyapO6-eBHlkn1Gtk0YRLW_k1p3YTPWEmte9jq-JsvtC3B6TYWX3clq_mJmKoi9es9sSYA6oiXqTRyKqJE9dS7OoLTvC97-0Wc8mzcZ-xyMN6jNA0EKbb31G2usgghjYSSSr7iU6-F4oBAvWUg-Ql8I97TSyAYkmzooFDeIbN8eH4EMlKOA-FCztfvYgLdGfYIPbU3skFV3N4TkTDJMnjcFnq2fMVFfnFtISkUZsm93m4B25j-Z9TgAAz3n8wjCkAcu-A1-kZu7hND3NQZD-_60T6wgSuIRmSdPRLxxuUCo2UIKezA0VVSuxMxgVknx4EyJOhmUNO3758vwge27vnCNgpgCPBD_MNgHP7g-0oG1sn_zzjsOjPKh2cghQuHM-dQQ_vTJRoI-OACPwrXPTgPiDgYwu9Mr_3fPL_gh4p9naO6YXZ65Th94HeElxIRD8LQa_eRJ-t2HF0TQY1Sq7i_pqUXx7GKUFlLz3GZLlijfWyOzjtfxldY91mSkWUFaIKMMDwUkpRnk0x6jaLuBEWWSlQm3Dr3UP37AsBfe0wYvT6amGBbo7OD-sAij3h_ecISo6VP73xDZw_CAMpqVTkxgexC2tSyrw35P3JaG-2TbB3DKd-N4u-NHRL1Xf7SF9VlxOBly3MYjpSR06hOIRqSYcxfnScRjBI5DNl2-MURe2AFqwmidEs3gL9O4GhcDapN1yp1dpI6eImdVNMDp1IOTzJM3rOlHnF3xWiePb-qeJqd2hon9FrM3zrvagrN6WYu_AYeRj1rARLRCc8p0Pia8L8tA2Jo3rs1IzlZ7IYsgO4t4sDUWW5UnvjluGVZpeNUqLim1IL9RuIJWRjvD3qBwGXJaPimNEK6ZqTnrXw9ABJnaCOXq5AuvVGK1RPIgJ7XJLnNpyz_XsqSIeow5ZMVAVWH6gc3O8qj7pU0I7zeZXOUUZiniyq2mEpPugrUWTyLh07fwEY3iOVJ-nx8McVmr2CpV1bFU_iYnDcEyILRgIPtLFCyFsH7O8IlZHIcDwLjFFqn3BeSMj1nI_s_jgkMuRXKeGQ-GNofBMGtdTFnUAR0cbkYOknQiQP9rZisFrgBKKrZ5z9Wzaezyuf5Jaqsjde5W-xrxWf94-PZDuMzzvSYQAMaNHX1VyurL-ZMXYNZ5_IXHWEsiW74RRCnc9z-eYWjRtVOtLaSXRJGxfBVdNc9M0xQTKPzYJWecq-hjW7RtbYzUD4kfCL3KYPKbiq_axpNWjSuAfz39xmhVYMA8cq9J1yFmsbpdVujJnK2EkCnHBoNXp0cJhnL73f2ZUdGhbSO5FqlFAaVbnV5ON6sUQrSY90WYcUes2qr-OuUBac-IGWR1HFJPPgfpXnRTpfxyY1XXWjZpkTMqfeOCbMY43tEvgTPjI&prev=RQ126CCE79F5F2ED&p=11&pg=105)

* Italy
* IQVIA
* Novara
* 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/074ab6030b5a182a?ql=l&sig=60d1f81ab9aa5512329e710ef5a4cd3f2c2c8276&e=C2sUkCZnq-NoaTl7bVu6gUVH19WBWV-0pS8UnYuIB3fn-sWVPtHpoNxW9MWpdKDOAjjdPmdSEFEv9PZxWIoXg-S8Lt2Z1BNV62KYjv3YlsgiBCOAez-XPvJZ4YO6XLeKWk6LsBMt8RMF_AEToZ3Zu1L-fLMZa5-CNbKvQeAW7SvMLnCyt7srzgikTebGYgsV74HzRaDdw7wQN0qFOKDhfVI71tRvHthy6Mm4ayyNEr4GN5UHHq8-UojjXz_TSskUHhdudg_6hROpVbsl_nR1aW84Yji6TKIAGB7paSh_fgANAERZHfLtzsacoqycJdyKdfhgX3HqNjTZQUNKiMsSY6r9yg5jn13jcP3H6ZjhPT-OMdP3r-ErRU3giXzTv9MiQDnKR0BhrrnJURiSd4NmX670_lVvvVNkGqp8SUpnB0ZPDFdauIdNJp0zl6chQJhSiurHJNsFqOm8U3zaqAFDNVeK3tpMNcM_i4RDxH-rDgsba048nqnU7HyJRVdUINCiFpruZgWWQaP_qSdfFCFX06OKGtSRBzg4GV73vLCiVwMw28GGoqIcNRlLCmlau5Bx2MA9pxv1AJkJkkvO8y4p1ninxxRSBhL2UQvdzBhUs9MoZLBe0juH9eHq8DmaxVADKsACuEyki5lYTnNAipUemrFLfEBAQny-2GD2OSuNTgLJe393K1EUJrsBlq1PcYNEirgpOc3pVznk9xMtCePEVK8XcS_CbLK5-SubbDm7VeBMNT3rj1gHhDiyS9kvRzXMAl8L3UT6ZSEe818Lqod706l3fTygImUG912qyhnH-QHP8sEPfL2HnC7PhV5jqk-IJBLSCCcavLbybYWFV8WM8HViWJvV7XR0TbkPiBAoduOy-WcLmwFX50vrfof7UQ4lgyZBmLPiZicuyLqQR8Fp8a80KmoyPW76HFK9iw6P3ZzmDsCGJMCd5HewGTg0NoZ6vivBGqZMVfn0khpiMFQzaUZZvc65LPdlgA5Xxqm3ADfkkDgYxcPr_oCWDO0rwEGPtp4CzlYEPBlkqafq_jvnPuSUEYf8Up9RJXExhbuvzYADtouuyTIeJkh2SaQ_bSGlAcR_rMAFf23qqoe4pf0UhD9Vif8S82RTMZuFiZWGUbSekJaQzavBEmTRyAI1dW0knQGH_7F4uG4KJBcR2L4wRBVhkzD2miEuBJ3y0oD1dw7BB7yz7ONOE9ATeBoSutJpqUTX_EdG7m11ZKVMG3kB7IgVuHimbWqSM8fpQJq1fBeAByQ4gx6O-D0-Jr0jmjl8EtxYZOMvfxb2yjrVRAm9VySOT62PZKD_ABtblPYwusSeviN9Zs2xF54ZWdGLDjvYrIVmz0av2izN1kgBsV76y3sUiswGdL7pwbhV9SP0x0BsfjxMgG8vX79baoa1znhBdsU1Wi6_2QQyL1wYL6AejGvIIw0WEnKjoX7uF_He1wHoT3TLVqW8NxH3b_XVhvOM_ntGEN9ItBEZbMVYUzxBow&prev=RQ126CCE79F5F2ED&p=12&pg=105)

* Italy
* IQVIA
* Cuneo
* 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/008bf355fbbd5b57?ql=l&sig=077c37643ce3c703d630cce03852bfff00ed09e8&e=beZXIX7IO39iuo40frYE5tZ2fqrak1_XMUPJyg-eMjS7HtLebP5AXLwjRHuZcCSg14izMiaUoOKMelbiCUHklOhS7DmRANRiEketa9851qmwWePTL1psIqjKxCnor_NqzUAiwQurLf8HF4A4loVm16u_g3GOZDTJHLYIgy3ElBD0VScNb6yqWsLZaIF0GgC06LfRFHKHjQTwifW7gitxi45xrK9fcei_TjnI-iKQXPBulzJa7wNzm3FnbFm3YuBBFFQMCoyIWoBqsECrzH287xUds9xja5_g4OKrw7iq0-i8vuJvfavxawp0C43bAxQILHcgI3evWJQa-UXtBxyhNzE_4cRRH1qKdYslU0NyeDv08ZNpGcS61GX1RgYa006PutVje1HcKjahNcE8vJDzsSGo4_4WpfCo3F6OxSYR9C9A28oXuYPYcDbrhKZFuDg9tI_VVB34NVbofo8ux4as0e9p7040WGzzumXgtwq7N3lIxj3iAA9DTP1qtIzYJJAIpN76jWkM7cv1hsD3g1qtSlJP0VVRY0HT1X-nTrU_uOXefCZfbMHYIy2O5QT0ZvINvInWEnzBj-qNGakG94Ng45KOvMgmRTvXIOHuT3OpkNw8OfRxdKPCcj_LkMiartxC0PV9Gt9NMe9AQ3-NZeth59Fw6X24q4emJzDCYxdWULDPqfrP9P5pitPUyYQb8QNqxs97JYCaVRgsAXY-Hn3YxVtcRuyR39fJza-su2Iqr-uvgbFDl98OTLcxGLKDRMldYdo6P5bd6eA6Wjw1SqGTTRMiCM8iyAZdmLm6cL4O90D4L6ohI8q0ZRCu7TeRuV0e2sjj-3kOGJ11WdXA9GHyNguxRkMRNRNpS99dOL_LuergRBPUgmDW5qwtOgA_NF_MvXkeqkt-CDRlt5Ly07SM3pdABV3wxHsmPQkO21sREso1sGy_F0xpZIZE2ItU1-otTzmJ7-BVvaXLdDOHhZuWuZbHHv1i1MeCDs-uVv0sweWxUaVVxrohNm1pPJKcL_JUUc6x3_NpLjEy5r7gKv5zU26zNQmwnOZeA27vwtnkAOH7rSab6jhChqnpUydiqBsjeccBC-IRtsTyfgV5puuZ5jCIq1QHv-Rss_uvFM4xNBF-VnFW6ipmf8o5hCVGLn0ScaALHlFU5eApk3G3QhJq4OcrBngT6nWHDHoxc-5fdTfErE_nI5RHwFXIKucQi-bMxAtQfpzUIdAtiILSEdW_N8IytzNrV_11Pz1uLLI9C8unZ1JXWQu1Ncc6nDA2bSf5cACcQRsIYYnbQYGbjmSBu5_sWTbXNLs8rDJPpaw0z8hsvh_HPSwrgk1MhFu7jWgETapXBnVpJiMQrpYXyDQaW5aOPphwRhf8d2iWYff4tjI68330HqeVxOFuah1zjTB6oVU5w-bD0Zn0J8AAgHgVaL5PD0-z36380O2mb88E_uzqDv2PxYYg-meEtTUWiFHXjVKNt5lm4Wor3i9Z7WXBMs4H&prev=RQ126CCE79F5F2ED&p=13&pg=105)

* Italy
* IQVIA
* Trieste
* 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/aceac5e03943d8e3?ql=l&sig=d6a4e8d5f7696a9ad80abc776007d1bcec44b584&e=IQsBLfiIOQj4Rzg3hQOntyTWFW4dwSvNaLPcaevb1pNuaLR2Ii_d7VF-tQ1LtVIbR-tNkACTPLRjPdCX0ieHGVaZmeORLxSDhs2PGRK2anLag_FX6iXuJTBxct81ugmnS2OsxD_Xp_3dX71zPagv2z5MgRsibjZKVMk_ikJ0PQO6BsMerEhKphPV-DodvrJy3I5i4aoKpDiI_83uW1N0bgLUs-Ohn398xDpdkPRucUvx2JFcv3pqEYQxfMztj9MccIuMnV5bORo5sqIkOSX2dl3FgLYeym0xR8NLl3lHAof7pxJwr_d1o-_yhfyBVTdtSyZSWHXPal5HHTq0NYTXYPgLFyEd_JfmDO0Lc75mM70fPCNBy8DLGoSr96gu4jCVzKh9ZCxYm4uTCnAVnSIEx2wQiPReQuoOYw914RATWvdi-ie4T5xMIyJcM31QLr04lrfzi_dAeOvPrXramQhjoz5ueBTrjlh6L4czcNxarnGVW9fsIq1az9nrMOwlEJmMdsw3j5P5csVxnnxjQL9BKzBm1S8UJngMlCYMyyAMc2uygh7ncwxu0hIrswri0FEKJ0EWm-ba08jXtFNA6X3VCEEpo63sNLwX42dvpJWKWmZkS4cMaWHPUMZ2HRqlBXaUMT2-_6YFS222MpYQ7wPqfpEK3-7a-yCPjyUaSLhdZSH2B-9IhUpplDAF8mIsFCJ9iKM2EOe_0ZIhwm_crWccAqVuFCLr52OeGnoPt2_oI4Mkf8FyePukCP1QwiQvEhzFfEhNSJX5NMmRRXLXLRoNtpn7Y0kbaKMRa-HdBcIqKcYscNbDssV0Mc7lpUqeUK9wb3RXl7WPSc6S48FQz6U4Je4PLNkUvkMSV91VHhJc_UxhZ-ALwgDNQY_C7w9v-t_T40w9CD9z9Df1vXzW7szzPMqgGVyk9lRsANfSGHa4tmowfOOsJyvye4j_v4uTE36bZd8Gvehw8XM2-EWqnFzkiaPagWW2pN8ktyHdbK2UJQJUCHy5b6T7beyk2cX0nN8Wl2vFYC_Irxixa4dQrcDzScILnHsH3Pf8eqVZAqC2atUCiYsNYjdC2b8vWLFxw4NWiJ1aryPVTu4JaRsx0YfHT0BLAvj3rIoiUr5y2u_e2u4qj_WJLXEi-zkuKzhlXEZ31Jj7xpOXaW5SwMYAZtehmxuGOSY9FlYW-XzAS4BcIs03TTu4Mo2snrVfPo2qiqxaH6ESwCbPa4pKB0-9m1H7xyiD_7r2DJIV1c0uVZUNWpF5oO35iF7k21eAeuTA2Q6XRdW5wrs1GOPW5indPzTcXdPUrJCl4ACkmw-Nrhyr2gGXRe4S9TIDV3YOxrQibYaC4h2_K2WIUZ054iNuLkuHL-pEgvHWrDhHVk7qLCP1Ep3rVGlpZCDLXEtgpx0HVk27jjNeau43qLUFqn07H-AVZZY9rRAYmH84Ml4r0TkaM9Dd80XhzoDSX9VrpI9nxRiL-Z2IJTvr9aTXwQgNU6FtbjA&prev=RQ126CCE79F5F2ED&p=14&pg=105)

* Italy
* IQVIA
* Rimini
* 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/5e968a29be7af97f?ql=l&sig=bfdc84a4e2e3db268729589c5c5d4164a90eba98&e=-4aR9nWxF_zfliEPo95ryBfPmm04PWgsxq7-Swuy0UoTHNIju9xHRvfq45D30QXiTAyjbWVM9YUTT7_gZgVUQrK5hGVMc2hcRmoJ_C0snSv1hxlPpXZAbY6Z1VZeOweJBftrZfPqIuTbwpItzNgSQT5-0Nuw1AWCpJX8LfehnXjTpBeRJmwr0nctU-JEbf-yS9HC2ylKpRgCh5qQ4mg8Ig78cytQkoFLmhnV2R6WTyCjyVKSI-eMuO2qDEmwSpvqYNzAnISWG_7tkZLUyRDyrgeX_LCw9seu8Dlf84cg7q3hEwKtqcOgI-YbyPOHhHXeQb4oMvIUSQAlkP2RmWttWVYBTgZkK5Uv3iaw3_o9S2XZoBAd3xDHGeu4efEZ2nFQBARiXyqC7OB_QZLF1D4U2_gdrAY0_Zq1bmsixJiLgXt44P01vEMnYRLwa7r0E8hOqYoko4kNyQwbVwNKsiRXEIhU0JNdSni0ZlBmYrtzBjrSDr64Sk6x8wzG0RWdDmLXQV4uHPNPmV8uTzVLj0mOCZxEIBzcjamiENfmCMW4Cqf2F0PjeM-xbJ4KBWAAgLHpOQO0o86vy0Y14CNFx0X2tBWFz6LPjgLyEG2nlZ9ZuxOnyYtNrys4OWzZqnjL2WNXS4WLgiRnzo-5j3IONPkgVSV1FZvlaqS1GKsD1IIcAvO-W7fbOe_bxJvCiP2oxa3C-1JKN8y2UScVGDRjdmUpq66oW1RPpuckOjDq73SNVDujUA6-CWs5G4Dt_Folrq_3KFp3DYfZ0YtV1CBWVDHHqbMQQAvMq4VcS31VmjgJbh-0AXM4-ZXlSvsxSXOvxibuGlP-dJnb1vRqwJGQhih2KJUr0poIjvyHcjq3Sx3xudmPQt8dSevc7ILIJZvNTGlWc0tppyJqACtW3X2lO_AmXdA-TXT1uhtdhDDx6zIk3S2tnZEUP_xLmtdEUzFbgR_EQCgjvXdVks2lKkbgUrkrcmSBzbOxlDIfxsfSN1u5hs4PO0Gwl-l9fqeFujoo3SIBLfirX8OFeGSF_wwi-5m45SFY_E9Pp3dBzPG9wbf0WxSdTbMbv5goUwdEPjtKXDVnDLWgNrwR_cgOmtNknp7768MV7RaKdE3gi-P0GXbnVAs_JMf_Ev22NNwkyRLH4cfYtkVB9DUx0cfrmmqRrhaG11ra07252b16GXf-_y01ZUnVmYeav_2cFVy9QEmzD7_a3DRQtxN4FILRtUA4GfJqiga2tI9SIX0-wlSB8e7RAqtwhNf3l_odCEfoLRqFAdNNbjaxo-wlcVGojESxXbNKQVTi4DUzsBescmrsuMzDYbscIseq2q12gPGyHaArA4-XzWrjf5JKh666TxjPSkm3q4kInL83p-lLUfLBlxvY0PJ9cLOWAv6Cn4DhYZ8oBMWSe_RVuu6vHcIHeH3l76wZckN-Kh9Rm5I3Q8U_SILJVTod4QG8brwyutS1V1_QEXKSTXWuudPorfMEiueluR1NoHk&prev=RQ126CCE79F5F2ED&p=15&pg=105)

* Italy
* IQVIA
* Ancona
* 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/2390402adc1017f1?ql=l&sig=509f2d62e20dba67295a7821d3125333bfa0778a&e=ig-Vj39QZHAX1vA7ZhHqNfw5vkC5xushBAA_Sop-nMW6zNPR1KPI_jKDI08x8Xa_vMhKHoqSnFkKAL8rjW84J_jZwP1YZmirOkScCYmYWuKUSiZElWTZ9K2c2kUn-QI33ObA5zUDswh1OCU1M7pRYe7HHDvo-rxcjvAU9qHmo36LgjcFSWX1V5qy1yyqr8ZjPfAvqodEtLrKZ1H-Qd945asF7STkNB1-uKXsmLn4dMeMfL8abwO74I9YzCyN2wNtGXwoaxYsJkD91AvC7Bh24BMTul4oNj_SoBg8Cx5kh24P818T2JbgCETYx-mqiSRZ1aJC7oQq3VnN03jGQzfX5IsFdusk1Je2CRSQurcGA-p6XnwLNJVsuggcCKT7sUdE_n-SDyydNcx1X6D028KxRAB_c_6bZd8fQ63krrhUGBlB81vw5iX0uE62d3FX5Gi1tqVFFHy-OCeePVNBQl-dmkQaRtuzSlGnbgjvjW8Drn8h7bQIIl1JV435sF9UX1wvNXTyKArIQB9F9xyrrtiET6WKyFs5ODq6ytSb7dZHTYFVDgu9Q1EsX2kw1x4KasMUvTwHZ1hN63NaukdgdR3UUjh19_Q2JFDjL9zqnetTMhE-5l0rb7lNoI1vRKSrWdHvszrOqIh35fHY0A-ymxHH-6PaNrb4y2tIWxweESiG6X7_6wTDKBM03GsDeP6Ks5bSOEkUoRxZ1Vym9tpLUs7qF7xtxKZf8wZkUK6K45ZRhEXAp5H_PfwkiZuDe2In3ipb5LorV6Pvklw_CLJVPHKfj6s5zf4fqxOmeWJBF8yI3wj9TgPyLcB6K35zBR9PQyfydHiCgTOHu8YqLVLL8pfbfLTwYFUoQfuqhn28AbA4QuwqHNo9ecU86NzWJjrbR-ryEg4qoBW01CwxvTBN0cwa8OrqtjoVmFJqoz_sRr6aG_wguL6r3HQW3IXd5wLweYK2pkwijYLpAYNhr08E4YC5i826v1u1L6Pw9105fi3YNKCiWWK8ppfMApjS35T3by9PrXBRlwy0_OFRgjOrXCuucTa5Tu5n0vdz7JRrKd-VyAN-77eilDIyKKayd83h125OWx8gQsBp6NRQOFiEKHf6mHuy_LWIcI3imrFVV8AcO2weKZ2l9dvrBL3QQ1Ugb4uFXPR5lnS7wwL9nevnC7idYKTZi96U5RDr7UHr5LZt9_fvvdfDl4XfmTxKs6TArGLecPePGN5bVB-jilaNFeX3sWVN3C7i7y8cXP4dVwU9NkPpwRI6MbUcj2wkAEsfl6tJBBWVdeYdgb2ynYCojj3yEsF9LKR6WSxWVWukjlZWKcrpQrwl9AP7uykRWDmW684LxEcJNCi3eEe-FNObDvp4DpL7TUOF_D3ct8-Cp8IP2bTUBkcUjVEA_GRrdBXh42KvTPq2oqRwFXiPfB94CFITXR-KIqYnjF7n2h3MiBOkcG7_yjDUmnii14eK49DqKyk5Or7AdyAt-u2xw75L-RknzkEg&prev=RQ126CCE79F5F2ED&p=16&pg=105)

* Italy
* IQVIA
* Piacenza
* 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/7c4c5a54290bafab?ql=l&sig=539ba56d79f2e91a24b61670154657a68269cee3&e=4zxTquU2rbpdp_IedmLtX6D-1ok1w71h-LRFjoJRKAmjPIJp_3NLIJzDMFBXcZSVxf618PXmeU-VjGa_J8c0z_LBa_1OQ1fuHnNsTL6MPEI0foiVhQjjEv1-7bJOvoWOOzrDnjGXtyTC3m3Lvksjvs_z9dWEO_YSMQZWM72HTdkPfV23VXtmI1GbQEornSAYG-dxT2TTLirFn2zbPhKVPq3qg61ERbPxt-NTaxxxDw_evt4QIHFJgulAZ9mWogSecA1KJwIkIW7dS08ZVYuOuXoN3WdfYYi6rFSVbQgyU1sGL4pTNyBtGSvionwDWZKnYbzaD5l_i1rXXoJpnO8p6vd-kGEZHaR0uumzwTKZmPBu2AYhOcib8ToSsg39Ae8BlBir-mMpMCRBdxG7xN3d3kF81iI1Tf9_v2Sv3RBR5LRQPMjORijsLRJze01KC0zXuB38NdFb9oKt3NS0oLEHnwGifQnbNZWUOBRxYXc18_cey8A-0Cex3ICz2_yxNKyQzRnewzNsDkKuEwz6227-NAv1CNEQWbBnYWtpJurEX9qL_ujKobZGypTOyb1p7BXQ4r91H0uM_FF6dmdEJyvSvxrOBjdfEvPL5p4xreOCY_5tBhxb4X4EhYFxWCbcKHXr_XL12LsKnX9k2qiLoRxZ8rfNS7Na-iPo_xnzSh6grc8FhllBryPNwgOVH6Le380Bf-W7IDv40FWXxUn_MyVRM0V3WhuDM4vJnSd-q9Y1G6vBnnph6aEiUrq8AkgZzNkcxOmdLSnF32974-pdW_yUBsVKvQg0-PebKIE98HjToF7n5YL-VFPZQR709R81_Dqe_Ho5G4L408yveqAoEs3hOhcjKW8rdKohdAC4zIRnZG3M8e21I5UUl2tEk3-Y0yYsD3Q9m2tOOXqZqq7GyYPN54uZUbRnM_N5ys2ctG_dpm_nOp4pkViiq7t052U3crPCLWhJkm8VcjqaSAJgbSgn-oefAOB5GMNzv35Edc29vZ9pk2Pl_laXlxvor2otKnrh4uAGPmd3K_tphBbcUqJxKgdNIXTOmNLYwegvroTHvG2JPJZfMwHwWYduH-w3SltYXQoATGrCnYoI9Eao_nvrP-0TmoLYdt_iKA0tR29aaj3LDiW8ycBE7vu3LnovdrTaafDyyenSjbAHxEn-5by33fERX8qofFTMNDNonGsOpFDDFnQ4VFKC_0BIiW3L55MvunN4QWedGNo33drZKdrB2QQywu2OtSarSJR-_Bqr4YLo4A8GiJURVxu6mW5hVEk3-5LvAxz_YZQ6tCsE3h8SqUQcHS6MaqYeF69yIycQuMPpGC1RGjqkl5yJQ7daZw4Uxi9fXjOs5zr0NYDTiZENJzOx0xrEuXAPut6HBwcbGWsnWhQOc2gEp_2If4jRKstG9L75APcQDa6hsYPE1gsmgHQS1iZlcnpocYWEsAQjCj6PlE9Y515yW2wGHYogRC18xgemghEbg2f6x918XAyiVZ4&prev=RQ126CCE79F5F2ED&p=17&pg=105)

* Italy
* IQVIA
* Ferrara
* 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/81e343a1e4262b44?ql=l&sig=880a21ab194129d61fe7a11c4e0b874016fdbc4e&e=jMHuaNFeoooNP5QRM9If-I9rgI3Em5yZ4thBPPWERS-ZhmmiksUf9OG9Gf5oZhTZ01sgrqrSvjaUmElITvEZ3GpuV-VEck34JgzB-JBanhA0viEfqYQzwQ4NvryJNe_Lvs6yBnOC3IjDdzk0x_efsi_vbAofWwnYJcJTfbzlG3zNnmv1kV5Av5o2lr2YSlNx0sfTt89FSRrRK9W-rU_4JQlgiiJfXTtu5bYl7vcsXFGQhTbggGf1ldJNwzxT_mhbyfGspGMslKjsI8Orwo-06zt-_4DZHC-qdIh7eHiYkCowk_PMhMFYMjtTGX8Gd_74AQsLQApm8D8WGkgXnIuOBgOIjl-XOCWnDU4XPUdF7QSd_Imz1aOzIrgHc28KKm4vmEb05P25zZy-xMbO3bjqNlmQ2L4GoclNUY0_chv2QfSQbJWnq725aRtmIfczv0ANjGpcgYHbJR7bXj5XcajleCs7RyEJAqrAKK6KxmpjSJNMzh_9pqzUvVf2qugMXaD87vE858Ve-C2sT7aZazJj5EYS7oa76elnPP8LRLSPXCgY9JK0gqRo5PRhyPUetl3PK-VHS4EcjjWjJy2CKUUMTuGTQPjUrOTTWEb7AHi8_USiXwkdOS6DjrgnoMluSkNwk44XszqBFNdnZyQnVgEvgt77-PtD4ISfZGNiAVsSNt3FSxPxW2wazi65z5jGFPULzIpwpVuVWYuXCJTpsGBj-HVIOYa4aGZ063zU6ebarfn87Gz9K0_ZaAn4ACQFGyuosE0Eolhp0X5sgmFVTxwRECLEKtK-ERqGrR4d44N_8VGbvg-6m5ps4Zizsnei_2FasP8vjN5tUaTPlKKCD-Nousa60ES0wTMpxSM05XyYLQ3Yy2jmHzDlsVni_YSuzzUidv8sk38kYK2O8u7uLuN9jqw8BKa7CfzAodHl3zd4nvwzgdFgNWmY2MMgalCfJ0gweArvvwkn3BFxyO6Qb5e0WeO9wwvvOeRdoVekRlHHol-q1qDVsww_S2LVyC9TF634yJ_QARIZ1oChE_uircl6f05ysOq7nAG992G4BVVsF51j9bCw3Ex08cHPBrOv6Q-2kYurNspwO9klPULhyAdWrKOxkWXlU_DRdSXohyIrkAiOAXL2bWIUSmMJLsbWYqvkosAbwgdwZXWGo3Q2l63dNG9d2ebM-1RNmzljkYqHgu73__QXKCukUjX4VGwjYOq6SRtLGA5gwneIcMTrkXr3IC9ERA2d4OCz6bNNFq5YI08gdWExsax-QZBuyGxkm39M9EiK5QxXfHkOCd8u5tPHG-njO3gzbIdT6-KXdGl8QHBtpZxvnX0RWg0ZRn1FAt1RwztRYkFzq0g6Wbxi66BLbwkxILvUsvpHiqTk4jYjmdhxl1vfEOe7pTLvsn9th1zKcUT8inHL_OgOXwt5rDGwqRtWYWJoiF5vh1_Xclk3PHlqPwioNZuq7Vvit1bGDOtg7wruQYgsyrAltSmnJuCHpuM&prev=RQ126CCE79F5F2ED&p=18&pg=105)

* Italy
* IQVIA
* Cremona
* 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/a7e525639f5de021?ql=l&sig=269ce1eef6e1777125cd4fcdbd7016080a0809eb&e=jzN7Rm10rtk3iqJJJRtYmD6jF1k5WR7eSdGWPgbAA4bFDp1Lal1ruHLWFmWMiA6WLXXOXaoosKHrSnqu6uxOEbgFRyp6SzolG5T04SQZRbSt1W7ER94ckFp-W7-XViM6lZyN9mWZuhKO5MNXB4tjNdvZBiDjD6ll3RBnQDzoKT6Oj1GkkaiLSbp3E0v6vAXoqzMKeWFPN7IBV9GwkxoENAU7jTm6wwcOXPPAtvrfmqgwGmYR7CfEAjCzFZTwj4ZqFd9ehKnWHIVOHY7kvUuhE-zrgcALMKlEw3HqQS2Yoe2sfwKNAzrts7u71at_7_r5Z1-8OcpRtP6TuLF4096WBozPp2-0wDSUI3OLrx5YcL_MQP9XdPEHlMosDHjhG4xqOaTP6u4f5nBeTxzH2yS20sjwcwOy02lDSDQ-_QJk8Vw1cR0kI2aebaaA6Z4rlNPKEtErIYIhUz1C2JsxN8aJfexNUJq0B6U0uurjB6eks2xCD4Hq-LwCT_1RqiabCN90J5R2bO2E6bgBWafawT_Hxt0d9wlnW55stEtEwLunuLGxKweuN_eOa9warklbtzqTYygrOuNhlD8lRumq1xnDYANWemoNCTsw8Fx8IgwnuaclnBt_ACuKp1MPAupVvrOQEVfgBUYe0aganyYxkz_St3UrBFW_FkfEagOg8xEzHC_qCj8uGBahs7JX1nHXRyPD_m6AcGTio_NZ4ORl2SArxeTx321ELvXMsr56XkCSLHar4_FDQzNF5g-QorF5xgy5jmk7b3o0muO9Sj5lsfGPfibW4oxe1P4EY0ICtR5rNOE-fyuCXGk-MUxCXfvzukooPByE__mttW_SBLNTrzmhyRT9GnNuNyKVTKOt1yiNWzMCAauLtybuD2cciYuEzHS_NCE9IfZX6lNNzPZpQcHKlqgoaVx3EADXe478j7Pxviue3lHFhxq1izXMJUdnp4Jb79kxsHahHnxxwp_xOCCl4EiozwQdFJidCcdEM3JcI1NuImAmcfgNakgRkjLZ6kfjOqYXYl6-zvOl1WNPFDHNWN-dausUNmsVTUrbg7E9JraM_JlkIHotlp_rSnBl2kwExPRNm6SZjunkpd7bK9xjrWoeI8ZG0g67Drgve29Ap26qesG9dyv4pEs85lRehSjm6rZyd7gs6XF7MMpHNrK6eEgVRyQz-GoieIEXvnlcVj6j3YDyUbhooJhIc3Jua-RBhtNucg_aJsRNedYktvw-Su0QXPvOFh1LLs_Xtj96pGhNvBb3k7AgKbaGOy3g9AxYBN80FF-ydRTvUiHDAOSf_dmX_KCapFKd1StE0li1Z_noagXZIZCx5cPVjAPmmk3l-oCa1PEOnHUvu8yAyZw99EIdC0EfNahtjCIDRdrAkAG6b9WJdqagtHHFl4N4durhXR7tWV7ytVTyFR9VRh7jCelBIfDfbN6g95_zPOh3PwVEW-VRS2UFhwoJ9pf8RCNw3Xx7nK79r4JLpsbrAIcByOzOt7c&prev=RQ126CCE79F5F2ED&p=19&pg=105)

* Italy
* IQVIA
* Pordenone
* 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/d191f74022569ae4?ql=l&sig=e26f71fb3094477f78998f1d854cf6cbb30c3783&e=XiZKlKcPu_oMDVWJvE75v6iULboo-GCQdgEXb1Au7uzYFIn71YIg4DUHyCyjNRhHIsMPJQ-PnPI-2vaVY7_FnV6s5XOF2BPPRXNP31QuO0eIpRDJIZfv2LRcVv969Qs4iShqd3czwDcoCO-e_q_FRHXsbfmATYJw9-1AY_BYCY7b0LzztEkbusVqiFHN-aRPoHb9YOqmObZqoKRfvunrAZxWfKiRdET2AEgKTiZJlnfu_Ms8-X-1ye9qrF7LipM6WKmnH8TJkNX8ooi_envss55X7WuPzIDRgPFJr_3ONjRqLyCUlHLEPcPwiIHVxdeDaT_cR8_ICP_7-W08b_DqSSbwdUxxV5Xd1bHqDK9CNXTLjixiTl3wuPBHR7jRdP4VPsz1M9B1iMMEmKE5EofEsuSIQnH0RNFvUX3QLUF45hmlaig_GQza5jS25JjutgNid0woCoasxJgmrNcvwn53lMZlT-YFI1wBSBJTsp4mL_cVZOEfYm_0q3F8_GjGvM1mQeYPqRvlzxnNNSdG0owq50Ep-ubbtpUriNlEHBfGAVPXS7HESigsxl2eQqULoE2I_TuL7k9DdupM4oGOz4bxgKY3RX4fVFU0tndk-Gz7lYQpJRWVyO1uTbPrgaPMuroPLjmerPJEB__CfcDqJEWc2ESGs30jmXZS8K30jrFcXecM40TGxhmxrqNBt11etwHg6eYeTQTgit2W6sYgK3wWBB-7IS5HL4LNKNXXH52fQBM9VThhC4dNMKpiR64R80dGM0pUDs-pqIJXtJpX6WNso0D37eh_eiwUIS_SHKgWBj3E7SH1Pwyz6m2X_ocJQg03gZBp9Yl7_rU3CdL4jPtPYolcl-rD8zelnGgrRRO8OkgzdddItiXuVE-mvSU-a4-ePpkq-Bn4FFwDEQpTAyy8euLT7bUeaHyJpxGejEaB5G1kn3mj_djtOPnk2lmsZVlpFjvTjgFRFEV9gPfVjanRULUlekHLZPbI_yUFjapaW37G9RhZTPCOgcrjhVTx69evGxwjXRddKggEe-LYu3YKO6dKuPH5Eep87fyGUSGuT2OJyZuTD3712IOK8VmIVLXgOKQg1fm8keNkY5hCu_n3BLiURPBEsKMDsCogSeY46H3lPxZgfGHGtiWRbCaY1e51ZeWzgHmIepIOnPc2Vs4EcsN9ymFzlcmd4X0Rkziy2uEsqrmlCy8Bns0qDRsi3byoyulN56FmE6QpEgVUNU99St6c-M0dUQCw88aV5pMAW0HO1kS1JECNyIPWVoq01A5iDaxer3s2Yi-M8fM-u3nKZrJIRbutTb0jRgxxRT3ve4MwdXtOLBLcsmSQJSJv2bpPpKPE4VpglfYxFc8jdduhPSsN0TaWqvQ09FeEVHLBmxUPWDwCXso_vIsAKoEuo0oXwcgtMQwt3oTkZf_oMPY1kmzIKyy4sCAylBGP43WXdTDNsWfGGuYSxQBeUWsdHwu-Z8NhcM67rAilyDgmtbjh4i0&prev=RQ126CCE79F5F2ED&p=20&pg=105)

* Italy
* IQVIA
* Arezzo
* 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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