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# 8855 English-speaking jobs in Italy

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[### Project Engineer - Wiring Devices (m/f/i)](/clickout/5515b4a6043b1f5c?ql=l&sig=16c066475f241f2f4356fc513830c66b466331d8&e=oSVToNIq-GQCwmgpL7qjHZg5I4Z9khullpIhVYPrW-_vwD8MZyDEli-zv79rP7nr3F4fdMWr6ilDg-B0uZI5iPnumzt0JhE_C8uRZfv6DDgnxMl0VH2T48nPd3LL2Ya3-naKrgBiSQkH8k7tmTnzFfIXGnSuYYIG-2unF5WyxG3vpHk3todIgJfTVF9Ej6C7Z3YenkZtfY5zvPEWnQqNQp0pAIMZaOHvTtNLy6bk-cfpIAGP9zbxDCZc8HrpBvzVZjsCXtjXGgf4M61Vw-QsvD3prqqnhdNXiy6RTWASWOXFZjx7R9sGlFSOCPxJzHInZVHkZc16ZknXNKzy2r3dYxZHzhfgiiNi4mBMP4hyxIspncFL1QD7pL_gnCYfZvCpQ_6D5MLbGmPaB-iQQ4OI81P4pBXaVaPFwcBFDjnzcFM65Kissm9Ek_6ULve912QBmo14fw_n76FFBn6s6avWv4iqrFK1xCaDcyxLnvUlZ3Xuo6wdiFznJwU_xV4eiVwySnfA8A_9La90lkFLXdwBKdsghaWLmGalkOecf5iZptnrm0524IPaiUEWd-9rQFc7tleOPbbPEstl6wMgyZK8MBpU--v3MmoWRX-CAoO0hJC6YjnqGE2Psca9eUxOxe_nlgM5yJDNF4N2hRy46EwhdCK3ASZYHE7kj8z3oIZP-DPT06Fy-uTaMfWLVtolF3bEiDV4ymIYi88b5SX9RqvfDiebh0AtP2x2p7wsIDhoRWLkAFSWd7zz53GWJkhYcC8CwUjW-0EXVux3p-3-AlewyL5zmDEjJsuZae_R2Q_lcnp6lXSQDfG-XridzmtMI5apDVzKmsWEop09I7U70Vq36wqMAt8zPJUEcfPm0GkVrGkycCi5QbzpxSAUj9CIkgNoF6wuqo2zOCsddtfOF9HcDgEc_JeTE732GEVkdNVzAm8kw6jjeBSKnNEXKthyLRBA32OUt_dTx942YF_92eXQ9Dg5bo9nQOLbIut-DqXnpSzi8QYH6tRE0DiEuYpLJr9qRvG62pJFDkBaounCT7qHlhn6lID0fxvehF-2SQkk4yxyvbaLzblL6aapfdCv7CFZJZfYFwfwVH-RPm8Dk5Se5ev6xrfBvpf1GjAC_43rjOut03Exlrt_PHnS2uMYt_g4Pz86cmKtUGf3LnZWEOmoxaE7CQzg_V85VAaVobZ9AzJbX0ZdP0CcvbAYJ91FF-ZRNkVbWIcpA_pNoUXZcop0gU3dL4bBlqWUwpbhNdXJNBf6cUptm0Zrm6CUivuxQEqj8beN5glddZ1ozx9aJAo5cG39dJ0mP6I32gthQch3jRZOPHrIQvtAPN1YANdEu1Xu8oriB2D4o4zZFu5A1gsDM-HFP5yx5dEUvc9Lh2Qw1rtDmcY0O4Kkv8a0MTMBs9JT_-dF7czvfctrqorzIscEbuHE2CDaIpobl4EmbZRauAltl6eGMOE&prev=RQ391BAA5050DFBB&p=1&pg=104)

* Italy
* UL Company
* Carugate
* November 1

Manage certification projects for wiring devices, including defining scope, schedules, and technical documentation. Support Electrical Distribution Certification, liaise with clients on UL requirements, and develop test programs. Requires an Engineering degree and four years of related experience.

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[### Senior Medical Strategy Lead, Clinical Development - Pulmonologist](/clickout/64c1381a536b25ff?ql=l&sig=82262cf9c786f3d1e49cc7dad0980ee4419bf30c&e=-qA5VTi4SBrYDiBjIlaLxgRoDZOqp_nbvK2exQ-eEsUX96gCH_KtO3-42OpGMt1SZMGpZc34Y601aMMq30unH-8MDQmRGd-U2w91GQDkuSyKHuEf62tlO5ZwpHV8fnZb_1my4E8ZmK1cEj3vt2w-i3mB6UrxIg4m8fNLcvG71S-yeaxh2Pa88J_kRk7ZnJDXMsE7ob4M4rUQnfYOL9xPt9nFIrRkZCdcChXtO3RQcrI_2v9gKdXQDF11dzHjTO8wvkOeTF7tS63ul60imAjX0gicGMI-h0ubD4LYhopSAWcSu6qoHaJ1lOyCLzHeZwH7ldavYvEYAyC9LLd1rcROJ-_OShn8FCBidh-TkRJ49BGKhUjumnvyKAQ_fD_kqMRelO-zrdBFwVqWHW68YFM0xQ_BlvuCMcJeRyo8f7BWTRk2rA5vVfyPBlMpzIkNgHQDuE_wwxoMoFPCkr38lVsmvfD-jqqXu-3Jr7EVhPc1KvUFlb6w_OwYu6tQh7V0QYG60DTY0jGQJMxoDS5q5l5H3enFeFJqyRk01XuOp82p7--6uPyXnhnOMjNYhdzDG4P1V2HiJrBHF68cNHAJtGZyIOcx-PO6RSTDkJDsAcp5QuPrG7LoGd04PTjXQKXjTbM41pCZXOcAmVdpI_0UoZZzarpNU1opspweVin4UDuhXgKiVXju8Kvm1zCC4FhdBlsyH30U8_8tfnLv-_649PlSkdnF0JtHANC-xPCoXImb4Z7rry68fxe-QDj1Zd-xry05oqsZkTrFvQMSZt4ZGeh3CFCHnDendTWKFsJeQz4mdxhp0F7Hm4Y5phEmMRWm3jsmtL32cXSSOayRVBTgAzkKRGhb05N3vQFiQFJKxFtR-8HbWHWaFnqJ_S9_sFhzeacF1ISmkC0Rcgx85VNzDAEFquBlAcZjObQCaPiK22DTVTGb5_Plk4q1CFhi7N13iG9i3AO4lm7blQp41RGh6DNp15-dP_zNKVFySn_bHxvyFJoSFA2yYT8ifjhddRhjvvrbKt63Hh-Hn2rBch2300wyQ5XFFNGaED0eJF-qSTUumBdtlY2ZfBrBQQuh2cEvOXfN7VjDFqXhNGVKU8ehIRrBWLkIdEy-aw96mf__pucHrOkY-2vUxFeRdpQRm-RGCDR8TUpg_avzCp4tP8hrdOEKKPzvTFxmczvAKCMRL3hfzzuYIuwhCj30LgkP3B4oYQSq7FjLPRD-9v0L_8F_2tHLaei67HRgU350sn4C7NZVYsMSX6gVyrhjFfstTZQl0gBRMjS7IUGXTDXiOLfMzTSKjYcrJKj0kAtT--0ibFG5eri83Ubfjx1Dt3Cc4JnNA9GIcWFMQj0O9g00uCc7MSePlY-uvTloB1A2lCxIFEMnR0TW-MtA5NO1KVSGfHQLAkMvTvcka_1qxCBHxoZttJBUJHWF6NwAmfiKt6zV7UpmP2lT-KTu42GgtSZGYOw9-7DhKvN1JWT5uA&prev=RQ391BAA5050DFBB&p=2&pg=104)

* Italy
* IQVIA
* Latina
* November 1

Senior Medical Strategy Lead provides strategic medical and scientific leadership across the R&D lifecycle and clinical trials. This role involves acting as a medical director and SME, shaping proposals, and driving clinical development strategy in Pulmonology.

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[### Senior Medical Strategy Lead, Clinical Development - Pulmonologist](/clickout/89e196c80e79271b?ql=l&sig=0e0412f880ddcb9abc6e1ce1fe41b37e2d8a1d7a&e=BW7HygnLVapBFgoOgIMr8QYKOPZLEUykGa4xhQ4qRG_r8nlBDPMFb0BEyuCZdA7llWIMaG0rRO_7ODKtTi0mFp5b2n2oj4bVTmsYsLz2NG2nYG23GwgYHjdCLxzqJRD8OJDL8OZdiHOt5CzbgervE0pCuIvqG_uDmK2cz0rciUml6nAs_KygEHJsGnMj64WTb3TEDhyobFL_4Lu1or27SJ0J3qhr1mAtYarvdcxphxV4btXOSnqwN_ebPgIh88dC5zYDHs3B8ba5f7uYd4s00ozn_mrCbE7KvzQ0Hj3g4kGYcj3a-a8kVxAechTLv-sUutA4QDc1cuPoxS3Yo-8pvCJEzVatf4DxRSHz4LJ_nqHrjkIIQNk9xaDhtuo-2cljYyVvPv00rxl0putU_Tby2WhbpkWQ5wPdjv1DCU7k0e11B9sBqsb27weCRxKcejpiEyXQyV--6sHU9XuhEs1N6TyQKThh_U4yH-mMk8UWxc4BRJJi5XWczXSIYPxnB4cXUBstn8A4ckrgtxr0Ne7lwrla3FbTiSAOJJQEv9Tz__xU8p6aJL2RFtn7YH8AVeS0xbPto3h02cy6ixMsp0vbB14ts9hAEVC4tqgHvnV-9WEC5ED0wbfiUVZndV34CncDgylImXrkwQjlW85PlYdJxrHGdKXG1Lr_vYS_90LvzFT3zBrqgPqJ5F768FWYd1y5JEmqSwRGhWUTck8z-FKgMwUI-G6oXHFJAV4g3cesPwPPdV8WUUoOvo2hbbAyTiGFK_c3O3KHxIj97IU71ulYO0KNWQ4LvMfFABrxc-pmbix9NG5tME2yOwDdL1TO39f6YMfESPobCoIvJ2Fy-8wZm91SAuoxGAQkmebYEkNo8wtwyfZiKwRYZvCZfm9RZheRjm4rJHFZ-TSWaPh5UotSdTHITg9qAOr5yM-48ZTX8xaNzhHfal7lWYf1QOPxxQOJMls7UUwtAy_xjcxXrPpXqM-hFwqIIVKDj22MBGB8GXvbkIihRwutRh1AhF9p933fQ6--Zltq1mQh0gGqw9KdCR3WC3U0CDt6ztB-gVnaGb73AOMvqpbafZLprBgMWewzRuCiCFq4VeaqzyShlK-xZzp4z62aYGlZnzmr3GvpD39vbPgVcgEcwf0mY1ncjSwuzjxkow3yXVI-RjRm_s0HUL0FaHqz-aXSfsX4itEbU7-7iNYL5gLRGz7sxYAFGGOi3gh6PD1hbKORY8-ptO_Co7nVSlR0VCiSHtiClrMShirf1B38J6cdFVPSyAF9B75zNKbrZwPEdFQgni_OYXjZ2tRiUIiZTPd_8JAr8r5zPNxo7OhZMIMTjbDXg3rVxlX1vJ8NWJbXdD_rKZEa2VXVCl-0A5bXmirQMmoDO2odygRDDsgdMelF4qtD5pBXucKD95kD1IPlHBset6L7Nefi2j1IPJyATYsaZMfcG3RJJv5Ihyiww5UxfqLVsHhGy4pcGkQ16_0KF91s6mJvIhqR2hbaE7pyw6o_y1CUcgBF&prev=RQ391BAA5050DFBB&p=3&pg=104)

* Italy
* IQVIA
* Province of Monza and Brianza
* November 1

Senior Medical Strategy Lead provides strategic medical and scientific leadership across the R&D lifecycle and clinical trials. This role involves acting as a medical director and SME, shaping proposals, and driving clinical development strategy in Pulmonology.

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[### Senior Medical Strategy Lead, Clinical Development - Pulmonologist](/clickout/0ec5e19903a00ccd?ql=l&sig=ec89a9944bde932a1db64c9a3d650a378e51ee4a&e=nviYZsnp0A2GNwdq_aTUWqKTzGE-d-zh5cOQSfyrUoFzwbIe6KtFcaY3lxbGX88_mWwRBu9MOP7gufMRzOYRBBXosMLVi3M3fhfuJ0lCfXzGdNF_ALZlKsNumVvYtfZeWlo0pD4WadscoiuYhKu6VzgyfShUgLfCojw03KtdO35lM2D3yya1WjJQJLJxApcSouAImr2yEQhLjJaFblV9rESP5fagKKyIbpg1fT4W2D-Vz6S0bfkEc2AsP_X2rt_ScZV351HgDRuFP2OkcQvflr2yqQtDh7ywHsiHaKM6L0pU37YTAdgO5_sORdcxUinTJGvQGNleDhTMYZvPpqvEkvT2rWLKpcuTKLwYZ1A6aNQgInfydwicmSse1953M26vihtRUtC-CfIJhLS-hF_IdLH95eWnLqUgoYNw1g8dPKWwfIUmtl9IYsl03VsAO7nrXkuVo-Zr-_MLQ1_CFkG0E7o_n_6jjZgkLWRtiMsFcJyh4cVlHOAInlDW44WXCPSDiSgWhNOFc01ynSrZRGy1W4M40-q_hdwg29t8lo1n5SodOY30njzcTsA3ofh3rQ6odTczcY-wPKcE7wMeWAA6haes8Mqftt-Ne6DQgRAn2CrJ6MJ8zsZbbwbah0wcK-78kVJEoFo19Zu5yWDTU5Nu0zNCmje4nmNm5xXYgMNg44dmA5pfGs5UFmtmGntxqhbCMdUN4BEvg9U1fZDDHwjCbBcjjP2GMUnUf3QLL-FErDSXsC4QUM5DR8G9vTBzOSBneOp-QNB1IGJXUqBnYGmnd5tkE4_Cyi39NBjm3kLKKwA1kkFt0VZFZNk_iWq9b8St7PG2s7eF31f9HPs1beZ7Vcq7ZevZDNV4NCIc0pU1pw33SsyR4CA8X5XwqBFacd2zEgoLDwciPSKNKRGWrxseErzC8nTHWAPndDQRTL1ciOUAMuP4P7CqSB7bpx9VfuFzRIPGZ6nYFB7OEChINnx5gKkpeGqVJqa5fswWJDw2Dr8BStijYFV6GP4K4fV3AcTAXBkH-38lQUsuLZ3pbfntgGPN_Ix4_5ImETchywwpSgcRr4N0UwnO7TvIMayjg1vwOA3Nf-ChzW5pMakMG-nwbLbjlqu_yL2oJPzIpbwPK0YJqQFkH3jdFO8y2HMlWwn6hqe-9on8wojCmxSz8FsCskB_IcTaZBTz2j5fEjWV5WVicAkTJ128Q_Es_GhYoFpEumSDdg5DPEZgQklYXXNG7vpBncDT1DFH4aX0dOKTdXvwNHrry5LilFxaNfDgB_bx-L8h7Toc7LBSn2odv4IA9OBECbu6-Z3ncsF1cOhmezpFyr0IOis9aZfEYjUXLJ8rgYJCliWPGPELnkPmAoU79FN57mKp2FrqoLn0heE1zb8K-xATsHBW7CosyZzT4O3Ge7KKVewGYE-InaR2BoIXuIkQ9msvA6aE5Pj_fLxqL8X9BtQQbesQj2xru2DIFKgWTnbfE91aCA&prev=RQ391BAA5050DFBB&p=4&pg=104)

* Italy
* IQVIA
* Varese
* November 1

Senior Medical Strategy Lead provides strategic medical and scientific leadership across the R&D lifecycle and clinical trials. This role involves acting as a medical director and SME, shaping proposals, and driving clinical development strategy in Pulmonology.

report problem

[### Senior Medical Strategy Lead, Clinical Development - Pulmonologist](/clickout/940f536e8b739cc4?ql=l&sig=6e15cfa8d1d291e83ca7058f552cf40f8ccd4696&e=FwWhUPtLw_igxtOWn78gLWei3km8mieJa7bUEbDbdHETyctoDso3XEv93KpQIw23OFPXUHuIFJMg0Z10ykl4XMzTYS-W3pSSbm6Ol0n0pQc2mBM9THBZu4YKeT6C34v5RYbXpWvjdAJI6vbzBmis5_FoT3wBkMv0eAm7dDn2Atve37bLdS14zYI8VF-xXXzwDvQc93dEFJGf8mj-yDqFL7t100VRiUdoi-t_t4o7qj-ohEet8vIJ-7LqCbSIgcLZuRw5QBj19TsHuNJLPP9fkSXiizNVX3L0lcNnA4QSLisYQr2aaCBGSGt6AWfDrkwR9RXMJJ07FeB7kGjmTZR0NdqHmSUTUwo7-IGERjvBxyvNV2_u5xzOJF5KhWgz8FV7szso3tGdemLSnN-mnw3ESTOwoEJAY6XZz7SeRWVnjvkk8DO6OFJH3lAO0_oFXEyNyIpQyp_ggEkIaeyDywtC8L_YHv5KJYduTIBB-bySEbM3EVrW551Y_9k9j1pjiNSrR4WTww8dSPUEL2s9JEOJsqMGOQqVhuQ3dxyGK1c2Dil2-vC5YP7-P_6JxO8HWok7c_TOefBkCzn-b1e7HUnmpBKugTcjAxlzSf98-ZbAOxjD8H742N2pd5LCoFpG-qcUHdTduw4633Jl38jq4wi0IUryYuBhFK5VGmwpGoeX4JiSR3O4pghTnjU8bPRKaWodiEdLZutBzIh1-vPU098e5Z2WV2Pooaoth5i4i-sRbQE6Dq-nFN8N4Dly1b0rl5QcKb1-156epmG2ieX3iK6FNng1eLFAIwIuERfa8JScc_AAg6Zz16njMoAbUKZKBkp91-ksRQuzl5V3NjYOlr1-VOQCCfUtemC3JAOvniXrGZHCvc40xT4A-PSSilgNbIOBYUe25AxrDa5_T6q2cP0SZU-mjZgnNRzVENonPvma2qxPd4mfygJyJlwPTshaZRQHfbxDgLbCRt0C5RBGInvmnMYMCMlaRmcAiKEN0wLFQklE5YmSYZI0SvLGq-ot3b3t_YiJPIQp9CG8FUHJL9TMMQZGbGu7YcylHilsd2ufaX7dDnGQO8SfBHtql197O2ofzn6F8t0Zry2Zlvhnkp19KM3J8B7lyKDx-lOHdH86G_1JVj690vSykZCcMeWUQu1nHrMAruiLkcRwhnJPPmZY1xLQ2cA2kS-ho_1SG86K8Rpsw8120f-AGAmiX1hKQVtHBqf400hwCX4RI2v9CDdyBot0u4rhhZTwzMQuS3OvT18kNlvWV-LWLrNPMir5A4QZKCtr6efE0CPkcESr_antmba2L5UKd2wfUcWX7shQczCEG3UdOyjiDeRndmOVKUR8XXc6-6P9uqJ918EL_9Kk_gAecjZnujwyPGiYd_YDWivYD4gZZiHTNouQSKhtOcRy5VKk4UCD_DVle4gJo5uJWmI2OPLbnF_xTgOjVUoexDDoSsNOdJsuACu2IBOLA1-RdNuZi4p3&prev=RQ391BAA5050DFBB&p=5&pg=104)

* Italy
* IQVIA
* Pavia
* November 1

Senior Medical Strategy Lead provides strategic medical and scientific leadership across the R&D lifecycle and clinical trials. This role involves acting as a medical director and SME, shaping proposals, and driving clinical development strategy in Pulmonology.

report problem

[### Clinical Research Associate](/clickout/5f80606d9af18e55?ql=l&sig=c9e0f01dcca7dcb12561d81cd65df92d7c48677a&e=iUoXRzfnDTonfLl_0vHuJLy82s9Nb-Yk6gpgJNmEW0Pzv73NoGgGL0_UJI6DDIm6dXXsx8Ww81pkD3VXzvEHxZmjC7v8B1emJiX2D7bGrXmR9YeESuuVZTTJg-9TqEJglYIoEj_hS5cW15qBWHMMezBLQFxxwST6awtxX-NPpWVwZQfzCAA_9sEcP04QXWyI48G2ogBRpK-iQ7HiYIqVBGY4yCvd4kbBZYzz-aVhILRcvEntsnrTmb1acEoPznQPXa6eOZHdaZv0GTIgdDizaCqHIvDLG9uPtFubhBtQTH8G4_dQtyQv7ybc2HCcL3rq6MLSwtNFlRU587yGwsFm0ZD-JKAWZUqI9y8C_c1cW2YbfpOdnou9QB_RQeg07761Q0AyUDoDs98OxIOfC2v5q_lbu-tn7lGPM5d8MPofy9KDpddUhChJ8oZI6e8A7qrdbPkI35p_Vsq8xmBp-Bl-TzoTYiGC8Ud-u54LHe01Rs39zBdNiFjBIrpoo0bWtInxyIyP2WVJZ1D1z-AuxYWp2kxFhP_Ac0n99rLUKk2kJNs456G639R1E5H29L3nIvmwPQp--mALM52PLhusVhtdM-5RoGdSyFwiRSvV3bXtN_L1tB20DXv-XNZ8tTcdSi8OcRqP4nCG9gmnOnWv-zOI7IF4QnYQsXfplxyGdEJvXpfqWWyYUelEmKkk7N6iD0YJKusAHGCgXrVl0oPsUv0cOR1DPLNBP4ElynL4gt6AUKsinLEs2L16paahKBKAJmyALHihQoYgMJZD-tNK7tJFrqyypqM878MgivXLyLob4WFScH2DlabEnGyWky-9p9_iI21SMavwm-tY72_-4movvfpGHm2lUxuKS8VEtg-PoRcBCOUio99boVvx9o5-Yg96szZf8xnBpV5_UtSI-oedWB6jSxMFfnxiMq14t6WWGCJCDGVZ-r9CAeTiOO1siIlCe-RJwn9CyQ9cWCusUyMjJGxTyixb1AGYyp6BdgZGjoGK9PkAvsZRidA8OA0z55ag16qc9l2IhEdcLaweVA0RsypHu8q_zb2FPOjW4tS3TZx50HDl3zKY3Sc1PX2KSP12yFn2cIJJ5ltw__FlTG_f3lT2rN1zWwmllB1tJyOaWf90BPgVcXkYRg1DMdy_1nNXSmKIRxCxoCbc8VEIDpXMtA7GedhmnE0z6Vpr6E9xl7NVP1nN2Z_9wd65c_mcfI4OqXTLD4QDUf9-w-2WkA0VkUFtzPdOJYfw2BwbD3syRt-bNJQqVEe60gtZ4saqcVgMqyOCXtrUAqvAHdHPFe2IYZh6zXa6WgRi7kmGiQCSwjACV-dnZNntMloi1lF6giFTGkIjak5z7vLIcu0h9EkNaH9A0JCMgSMouoe3yhKuTpkG7K0c8cu7-cVZi1E19d05hOWhorTGmmg5vamK26KXr-QMsVYr5rYQGLtizluoeZ4VVEZF_uqKKTSE2r0KWSdKV1uv3V2oL_Oxz-ntIeMQ&prev=RQ391BAA5050DFBB&p=6&pg=104)

* Italy
* IQVIA
* Rome
* 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/766306fae552d527?ql=l&sig=42a10a159f4853df9f31ec0a7c82e6c4f1eec788&e=qGN2OL92m9u7GWEVzJYQUIwYlS-QhWONUeWGs10XcoO4wOLixrnpSb9AJQaITxfL1aGg1K5cvIS-GhnSJ6trP6z3cxAZ6OwnSO21Wa3QWTCOTOVx11Pabw7ax2MB1-EoyHNpvjnnGupxLw9B0pat1dkNiYQ4BBodrwX_eWF7JlMOKYCPhx5dIfbcsmbrCVXBPwVxVmdjAlZPRdgqfnzmRsVGSjuYxxTPHFBmzdjceZ7bNzHnOdvqmF7I-zpc1lP5WdOJ6p8DzQbPC4DFjv-B0kkesDd0lXg_S7PU5RGLIkQHouSYx8-GQjYBYK7RhNwQQhJ3NFDmAGzYyFay4DjLrCYgn8-ZyJad7PTFYUNpknHcOkQVBIPW04Z9u9QQVlnxFVIociKp4Mmu5UPz9JbXXiOUr6ICJ0wubGfpyaFeUJgeY8WX14WhwxJFVGvydqw1NDkHBrvF3v0L1xdFAmtsrKQoAtz8iDsk8gqh_Yu1iu54Qq38GZgSnpCPe1VfpUtx6R0B1hgpHMTRGiesC6DG9Xf2j7RN49hwZiRixvzDqM3z2yXGqNTsesbZRLgTFPIL-qSg1xelUcqH1jomg-bsjVpe7q_Prmz4IjKmqZdzsVOavw5zwoG_q-z8R1np--FuuEfRmm-_dg3LrD9kYJmRvQrYVGkjZ9ZsyJ1THk_WG8tjJonbbIxjrBQxIfUwCkGYvwxdZen0MAus6Ssjji4JY_8jfiL1SSHrWOdj6dlXRRpXefy_QGu_xD_11q0MH61jVNwblpddFy2Ri-mOOIDgEHvKL4hbOiEUX21fyTHc5QA1ptsqHsQQHjyUi2VjJqMVV26H8DUHPRxyKxdzqcrV3-Wxu2A-RhOfhQfXzQ2EY94sZADQ1myTCV48OTDANHxw71zCXzjiyfp4vH8dJQWNuNhp1XtNnmbB3-x3GjR18_GHLk9LyPbNobne2OYuxd6le3DofQhRuyLrfQmixtazXdtU6mdzn6jLjqZ3XHXy29HbiPGp7ze7ozKzDK_6PV6HMzY-IFhQJntf3bQqlp5rdSoWgtzR9S5dbpQe4EmYNi0E5z8SunLmPPX9p0HH-u0dXDosYGPHf6Kc9RtdH5LaKV-Qk8R1PYHytl5SSfA69C5IuclyCCJoXltVoarSAMHhCeb7jp5kKZ2fDWUWfZBowEEdk_QhncUGK_2sSF-F8worGTXBaX5oBLmQWcE-l0VmzEj9m5vQLhXNOWd1xZcsNgj85ewmP1sr-91tbS5e2qE64nshR91_qmuZkEc-iULxXUOgyoer62BQNa2ZrvYgD0bxpKDEakZmuOaaqmqY6BHlJJHYS9m-KR4jxDsmq-oclrSwlcVnIrVkuE21W-Zpg-fgcaZ-tXZNgqNX0XCcaKQZz6ph2dUUe6oxEB2vNO1q5iQep_Ejw3Ed9DaiyH_EXgeP1iwhghaJzzzynCU3ycikaTGKCCHh-nVKgx-RSkKSsSjkrhQkk4WukjFc2_OntA&prev=RQ391BAA5050DFBB&p=7&pg=104)

* Italy
* IQVIA
* Turin
* 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/8086dd7f7b9f64ca?ql=l&sig=b6dee72b03cade2316d1d5a709d5a46a8c5a8c84&e=xe4zoXQfpsW7rprQwzTUW9U-dApZanL8U39odD8U3ElevumMfKLa2GuzPmyZ0EaDRIQsKlmrYk8PVdwV5fqCpldto2q3d11DXvQc8ZjQ0R1NnM6tmwC2MzIb0Pj5gKEnt20a2KqCIwQpe_lkYXHoSex47YLLNQO2r41nGAUiAT5i3VXuhAl4AhZOhMIafAfWOd2C-v5wTHOwA_fq4HQw9__HAPo1BNcFtBQQvHH17mmytPQgyVG_KYzD9_OgOg1eIw5qkr962ActgpdGVbqHsXW5TseqSI28LxaglVu9pnDFOizKd1_OFQ1xKXFdOw4pCL6HiqDYUK1EON-hezF4DTS3gjlsiifTxp1CAhEox_FobPoztZKtAVtoj42uZXVLmkDipVpAH8d4M5Vzk3cxR7rtMqy7o4jU1cywZVxocpVsMiTTXagP3TNh4datjp3N3gCTtj10-W91fSelj0nd0LwEIfCHhmu2A_n155_qAGKtjNEWvM9NIKptcMSeHIchbX36Y3jpNDuzqMn-QrVjTN3ns76F_HPGEJ73QmcWA4yge7nG4WvvwPSGnYxVrnDoLBOwPNXOUilGDwF1XD2MHk1nd_m5W0KUjVCFsblmqr4aoC52tHcZobjM3meqTRd1o7rD5mppZsX-uZKcZWiW2vKtkgJkzZiO8BRR3xsR6MBHlTZMntNVyeHKOP7duzhoyIrIdF9qJn3uGio8MhGO3DVgnrHhIk8lvfTiv6fTRbvI6xBS-EK_a4pTos0RHfADZ3wUZeQ1pyTXg6FbgafdkHZCX7lmXM1GHdPgiJi89xtLBpDcKCYoVsoL_FSkmPU5xphPF-GEMOuinQ3_xfh_RuvjkMxpdkDZW19QPNYBqqJgEM_8BccZ6XUUY--3mUgrHBLBiUrDbUB4RlTi4UTHN-5TOB0-qb0J2qzFpvHmyXHo9K9_dKUbKwm66Ob6Sg6Cz7UPbWC4B19shtH-yDJLI9ZyT0bROnsWUKOtp40CsTgAMoNWjP8d4NM5-N3KvTiDqsf2zZfblEgB6Yv6ddGtkTDcDbZCxO9NURv5VktGMHnFs3LxvmarBHcOJsLki3RYad4fhArv1FtFgKKiBnPQ5Vs3oJpFty9LKsgBwu92omnTYQRdTsVngcasoxs2T99EtjR7P-4d-4P-FE60DR0HppNEujDldhQW0RdQnUc3T3tbPOJ31QVE3LNId69h6-iI1DmGqgwsGzmKwOlEBqrqPGqgMEs_5i0u1wqfvP1ZDkUnHnBlXz2t2ZuKZL2c7WQAwIrvf56Fxa7mxoTCcatKT43brRXFXbtH-y5_Daho9sJqsPBGoyS0knjix4m1qUx4zFsmqiH9rKhXQuCY7F1zWqT5LrbBTixRilqSxzgxHV7OYkU9JIhY81CDjFNvoBbx1el201Q8mM4CZZz4A92dHchqs85lR8wKB4AI4-WYc9G0UoU-noO9OL3UYHkiDIgVzLSRPFii7ggBJDvQyO5tSYTb&prev=RQ391BAA5050DFBB&p=8&pg=104)

* Italy
* IQVIA
* Bologna
* 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/954a1f78453df8ba?ql=l&sig=caacbea5862a4ec0774ea5132137fbb503a43561&e=SQoDiAeTcN1_1-5QYEL7nH65fClL_OMpYInRQeKuioAIgVWSoGK8rEdJtGcb4aCNLXThD1m9QGy_fF395x_5sTJDrF5bmUklTTy55NPO5JFK84ewbq7BuQ0udBzbrg46Fe6DJY2KyLi1mSLlTsibq4wM391zJzL_gkIRP2YnChX5dJwsRA1-Z6QOjDL7A4GCgDeGXMckERH8KX14TsutKhx6CMplMw-5zKrT_PEZa0iJVCRlZuOeMulUz_AGTF14IAEuUlNegw44f_86-WZnaah0Dtm52k9gVGxKFFHS-SNdgLMTzavm3ix8k0gbh5FaOVrQ2VMy5lWK5P9q8vs7gu-ul1jacA_rxqsM-gpIxaWS2oaBfWPHYsWGivQgYVsq8cKY52lvdNyvBYk3NaZHWucs1x-8-3O0iC0z7h9vXkU73uuSjvId5ebUMcBc_Z31SgwjJDxuheCcjudH3uN46FtLKbjXNw8c9wa0tVHk3_n_Hkr_C3cUOf1ajvLpak4rcHcqCNzKwjlbJXJGV_5nmPSInZhSRklPx1O6A__Eo_s4ATxJrFRzS0tKMrYyQQU3h4jQkR7MZTG8IBB8hlyzZyDQRgNMs7rxKGtOwMct5uVVGKJr4MQU5EoHm92jluSHyP-z4m6NOKC4D7rV7c3-_B7ubFXzg9VJmI9UxD-yY-fMMM41HegP70fxso5WelRM9EHJPAzFZWFsE1SDNAFRoZKvQKhzRu6E8bVKLj4s3z-QCqkZkQDUHV5yePuZDagXE30Xul5LW4e0d_ZetasIXfN1dbiCk0QKCwfVq_c4DYJFAon3Rh2nkk-uzj8UlE_7erCDWaMlOxIpO5KrnZL6DOU-jY1Lxq2f9Um4J8IyHOGQR68TvSKgvprYLZ4x_19a3goKRAP1joZ9wJHC_62L4PJ4EU2g4bY-tynNqd-UOFMEKOZgKWnGHi8UXV9FkVyQyJ0okwFqJsg49C5zy6A2VqD8z3pV-MxsHJl6b5gkHcuk1zxLovC0VtZG-eC6MwlRd8r7hoFz15Ph41VOKPY_9EGoKPIJyiL8JWC_Bqdo9_IWkwPW7Ge7GGF3Vjrc1SGBuIHu9KUESu3DYYh_EU8w0Z4wVVLqcurFh-2t994LV43GwOlistB2oOO9SiXHyjrIh11xm40K3utbKJfcGH91t-CKW5ZqdzOKi6QiSikWLUo6786Vu7x1SXDCGdKx-EfjjDbYwADL4zEQPPBq3bBz9cgXV8-XgfXL7xHE29gFgz3eFIROHLqytVtJTd-MKXeOhZG4apN_9SzS2hpdGqkVgCadb1aCmIgcDPyklbaIenbJb83iHmJW0P1eTeYinLRxJMU_mIYXialdYH1Art9DR0CCnv8vLxXuaesIupr2d7wn_lFiYbeiMLJWmj0QBK78ViTATyxCv13PLNw1eJZoO5y1bAESeLHUWvQUqSehKHVby_4P_NgP4zTeWOzs4F09_fWzTIhOBNwK4_aTfAZUya_byw&prev=RQ391BAA5050DFBB&p=9&pg=104)

* Italy
* IQVIA
* Florence
* 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/86ce8bdce16b9076?ql=l&sig=635fa1286e77109feb996dd5305b40df5177a987&e=VFPimcKBCwZAnea7qkX036hKvM1bSRyrlhMwJD7uazz5hpaW_hhJz069xdryWBGBwRs15OmSNJU7K3CsyDNkurFnkIE0e2vOpbT8fbw-sjh7R69Q5ik7Rd9gt830DxTdO6EkvfIWYTrAqOsrH3u8iT5ctEvTAX_SXb5uqEPNg81DHYbw4I7x5ZHD_V_-ILByRy2PBS_t8gpN30tcZi2zmrAr56oUa_PbKRE8pn2MYX7cgph7ERpKYWlDu2q4JU-63lgfCO2N0dWbo8oSyowQA-75SGCT6ti421NCPtXQ7WFp47azhV6OAY_V1mTloRUICdeRLPX_N5XjThPBRh9Oi2IVnlT5JVOBj_j3GrLcm1j4dghzRYWACwa-IihO9IUfRYDAyct9viW37xjr_lUItsnrl3XMgkau5I_2vtkAF2lkIrC9PTL4WZDQU9ysvt56Ilxl7wjMG1rPlY8zdROPWbpQXzpaneGDQR_zth6wL1A72r6ELoI10i4zHRaB8eGBKq9n7RVs4jHfr4C0NF_MYyhrhY-syW8zeUe4jmvh0DOQKTQBPV1qUDSPS9uIiYtKKBtaoZWzsO_VDZcHMf3WrPQmrJKKRG6r5dr7zZ7_jBF7-poZbnAWflvYj3H4R8iFGx5HyKpdqBzlQAWPNutUoUw5XG5dIAZCUq4pOub7IGp9E4KAGqyrfNzoij2xPj3oMqbBlBsFu8QIGE1BMbelHtn1J_I7bEUtUxQpc9D2-4L-ZcqCLcpLOrJsqAstLjHrjjYM1EiwUxTz2obPjX5jiCIlK9XZH8yA2D1lX87WOlbja_r2MpyrN9xCkLyFLeuBIWPTtuGtz1h7xqYFJgCO3GToUu_buOATYTQSS3YqUf5EP9p68qBRYxgVm-tCG-oGvikdolwcMOQKVNXy3haOWpyXEO06rWcs6Q8dF9Fs2ulI7F9xhB3try88gjPMAEjN1UDwaQxdqxzzXDLrl2rr_AVBlpwz2ARgD6XZ14fA6iaFR23XRtZKo-XYZ3DRFp8a6DzYmxvUxO69va1J4t8pGtYjTjz_YJAR-LpvN9gUP7fsybCjLCc3cX0qex_peNM_ectPIC2xROflF2CVXQ9IBTGQzekagf95uGJq-FQ0qo_vuzYuXDiockJw_2O94mCTJS54-MDCPuBboIRC0dXk2zhorstLRBOpuz2bqP123Wa4GHUOGxirSVIXqntyVEjcN2z-oGc6PKXKKbHFd9loSt134Z7KijJ3lullZKlO56C00BBmipAARtiox848QuDd_Cvl6RbKIDNG11UdMUGMtNSehmZnWD4ULSiXX-qbBZ1ikdv1IBVEHdQuiT0JwvQUAtjQLIfUssWKSH5eLFccIBkbUNWeuDYrGJU2mQeaS5B5s2czvY_HC4PUBq2aSf7zxtxPznAejAyIcKRxwILD1tCH97lOeydxQhbmeLD-I6TslXpJP0xadlt9-v6HPzhhb7RVDM6NZAxGODq9S5ru1jw&prev=RQ391BAA5050DFBB&p=10&pg=104)

* Italy
* IQVIA
* Verona
* 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/435b2b19f8a32e91?ql=l&sig=55dcf59bdce85e882772c3e71b2a1059def65ad4&e=FePNDlsAasMcsnLL3cvmM6xy9dM3If7NTv-EezuXQP5oMN0beNDsHPeE80IdQp2b1bZ0ICVG7k4l5e3s_YakZ5kvTrIBKzAgZwhBfzky8LiF1g6Nj6uc_HDEnhqURHzM6PTtaQeJ-QtX_dYsYkXtDFyiYU5t8YRCjCdlM0qWYghOFpu7KbMOaftdW1zLRj1p80kQ73tNyYOFZaH3ZLFdB6jJ8kl-otaCqAq8bs070CnRtIeDqNGqasIoxpD98F6asiJlvwZyrKJ3YmZIc1R16gSA0DKYlXmtlrUt6crUbEJz2-FmxvcvK3GWLiAzrr13bwZ2RXQ-Y5c14b-5tBAmbLBVhTfY84vEZzpsXvMK9juil_H3oRfCZLq7XONfYPWah4mPlbzs8coHAseDmQ7OGt-n8mJu2x2cHvS6gWUMjA7uL_9p-1UhHWVrf5E-caz2jgEF3N_sE08Z8DFmOZhgC6KdYyJbsBsQR3xiCxry1ox0CbJaxejyCF_ri3TePIOCZHBaGubmoXc_9hb_bZwE9npUXbFEdmymmezQfTnAKd0afAAdhFqJUqSnPcPYu3ytp_X4UCUr2p6lRp_G0cZeXv8wyd5IZwfd7x5CdcUtZDg6LtmTjXGnuwpTj_yfdbXVN8OaYoyREB5UsB9nGQOsC024-hoTafRacmE1XY52s8wbD2m5QQqPkHq_qADOocTvbHrT536Iadr5-Awra30BYSgjUD9aFjfrn3QfHZ7B3QSJ6MXKQzEviHbGxVZisLu-KG_4Ptm_h8eAwWWUjomgojiDokBJ9Wlokb1MQmROGEUY8YoACsJbNrjZ6q8697mlwurWHqen09d_zk5dxARciUWr8CFLHiZqmxNtg7OCi9WncrOFaZkS0t-gDDjpZl-y-YZCG4jriZDGGXJoc2GgrZPs25qOXKV7V9fiNQ8GqBWcXe8Bbz5OqILQKugah_KQl2HIK9aLrPAPqbRfz9pP5EW8C6RJwJg_j-EA44pRa7RE8QscAojD3CdHhYzhiJn4xH70k9_gPMuGTv1G3VuPl9rGtCTJII5q23qi0wsYrNXSu-jwcSYsLOLuwDAbQ9cJ1vaV6TzDPPk8kddy05sntTiomuagqOUuYJvHI_c99YPj_CHLlV28w5uAIfeeJZ3iJRWtw9dSZlWyFZTQQNgfpXa-LdNqdkRh9gncwPbKxr1n0KjFHklMR14ePPDR7MfytY9XiWAH_s9u-72FVNfze4yZWAD8YrF3FvdHbbLen4FZGPK_6S12HsV2kdcEGH8X9iNvZcGcZ-niD3jq0uzyiAnuS88eHDAujWgQuyq7YM_t4vgtmbqFKdepNSmIdbSWQIbaxZnoQ-pIpqp6pLo236sGNv7OaNMWBxwz8oiPBuoONv3_YYmeobiYfle0joLUWD4H4IaCDyM7XgKBSXzet4ek09i164ox3DA4_tsWoBFg4qsk0BmWEnFWw9nPYxwy3nDTnQPbqAfm2PwZXbjinw&prev=RQ391BAA5050DFBB&p=11&pg=104)

* Italy
* IQVIA
* Padua
* 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/872a22ec4cc199d6?ql=l&sig=49a250a25d44fcb341d530ca5a65afb4e4e478c1&e=qo5wS4u0j_OXcvy88-s5Aag9PompX06UHtPdZj02dj36vSPY27mvGo6K4j6ya5AGbLG4xy5zI4VZ0xzyONqRVZW2y914GmrelKl8LJ-Ca3_U5aFj_vJ-IUlLD2aRFPP8vKPIl1lQ-Mklx_yN7ckr5QCVL9R5Q2VPG4y9t6Aw0AtQDunySmd4PkdMQGSHxwsvwSzYCcYY7eyI3TPWVYlWqS8JwKYeeELmsxHSwZnuLHEX0_9TLTIAU_Q-x2jRxn_fjn0L9srULQ3z6CYB2bSyGJUPF_RsAIDGPrY7zS498skNpThwfuiiv-CgwKy-FXNiqwEhbvAT_IYoRHHfh2URZJ01xPvBwwFwgfLK7dO4K1FoSW5cMxlBkp_Spn4N98D2usWxvLZtryQZ8PbPm-gErY86RM0Z8UhezNNRy4B9tDuBgwE_s--kyu4dm-EZ2I71HezWY9d1aFvX1b7muD_b2nJcWrmcpGy1bxxO4A1vHg_F5KROsnPgI9VjsERIWzWloPDYXPiYSfq5pvukS9NHM4J_hIio4_e9Jq-w2kwjY6-ZgUztXojrqmHXqRyESMh-7ZUA9D3-53qt45q7FLjE7ifP6DzeCvBeKkFCLS7u0wHJS5_tt8jLPDEMnkB6xjnUYdbnMFdH9zgreeGgGUaxbW8AmCytgp3rXlsZLMchAfOMJzAcUhdLaNfjR2aZZ85bF3e0p9FoPXBLkaY5urHTzRsWnv5xxvRh6EBxU1KNkogKgM3j8RdG1rp2D92hS_p_b4q8gK6kaL2zdTi5X2LZF3SGNjKr9mQ2FhvdYbLkxJFiFv0hSsAZRuBI09CddReukztwQHK53UMTVxRCHeHOt2qHTzy3Ux-14NYPoQn788ageOnqcJQtKvHJg_A9a0dK2bzt-_JxcVEKOKV0gweOoqGnJ4WWHuxAGbYV8xroW39e8aJRRtXrEx3-4iHEdh3f6oE9LC_Rx8ho2AlVbkRK9a27x7GqIQScec4gOTMCgkj5wkA4PWcIbiOi20XWd-WKdrUt_uSh1lDDEI4Snv7Jb1y3Q1NChQNY-WB-5xYj4ITj2eIAS-kWdYQqFQ1VEO8AnhqJc1pj-QVVPGFh2YWPWQK3BVgKrvDvOFK9Sa5BwMBR23tT2NOycvGu9y9RY_Qm44e3J7NOctnUjT1bqPOPImDtdX2AZjbq04F8GGUUovmXTRpDMVPmhKOhgKYplEy9YhTYG9HIU4yWJz6_Jrwl-QSCAAMgljTntJnTVZ0nap5L9D0LwnDemguhMlIly5CnnHttyr_c73wI9-d7SJKlxbBbs855W9Mc96WkU4bz4Ka-tA1OudK6fAhyr2Fu61C-O9T0_twAhnROvYHg-8FebAopB1xGw3vdAn2raCeoUwp24E0ju_ZsISOWrQ6MDSml-AesDlkH2aMCeydaKjaW3W3Y4BUYhaz77CKW3NiYk7QMoQWEr-sKwJIhjfyjPM8pK8WsZUwEq8lWYCvXBr3uHg&prev=RQ391BAA5050DFBB&p=12&pg=104)

* Italy
* IQVIA
* Genoa
* 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/efca4bc2e7589233?ql=l&sig=ab97d536065527065ac4f79def1bd72619d43866&e=aapqnPVW4Sdc1obA93ayJpnLeuO3ZeJLROCyXRv5CIlP3sEeZSQoyIAlsJJFnDoUn-Rd-hd5MQl73KS4bcQIIzF3evS40E2lNUDCONVnE8dXaQ0cRqnuTTWOU16_DPW5ROKKBeDYKVqWtYpcP01nlrMiYKnWJhIdtYmnEe84qBF4OupedtyRFzbZjvsmvsrGZYL0XaTPI3Aso0fsE98sNYu6f4TbDVWq5HeWSWYqaXB52UJf6wnh3zn05UlpabsQfs2dfWEshNhZt23Mm4XcLjZvZLOZeetO2yoZzo4TsxbuTnvjCoFdJyh-FmYA5lTR9PEE1H-2TiLH7GNC5VYInfvbELQ9N8H3aPV68pG1cbHwPGaORHdu7qbLJgCArBezF5Nee_6CIEXluUg4-zuoM00efqBO_S_xSunLeralI2P5N6n9jzE3J-_4CvBKbVYnxWMbPVCEDompaRXhU1YlQYPiRB7mHuq90k-ZYZ5PzuXSVSJMmbIn53hANrhdi2S5spDKphNxTUZpcPR28cr-PX8j5LpjhCwfusOaz9wtGyQipmzicL-fnFpQ96lX12C2rDolX_1caBJalc_wOSQiIPOkW-iABYcmDE3E0qVqJwn-kPe1oEhieQH_hi9VWAHFw8UgiAa5AbdcvPg5oO-rKM6lNkPZpKEAueD7Rube8p8oJlhXbJpPYCTO_uqe1m1Nnl5Sjm3hdWEdVohCdX9xQAwmup1ZMg4zyQwO9d8mOcfAQW_UToFhDNoB37fz4fV5MnVTs9_2n0vldufVQUQb9cBceB7yhzrSeSBCq8caeHEhqatM3nmSe5_Bm12RXuvcLAjndVQXih7XuuTFX7EK4Sx4y57_ho2rBr6otoXrpdd7DcdS_MSNr-UBBAU2vAJVIf_jI4Hi-3-H282u5OLZtPAtJygtITzu7QH0fyow9pNyyRbMHJfDiS9V-GQia5orPv3m0L7t9OLQwDuBZHVbxx1eNvcTcJ_sakremTz1_qoNtZr6WMZuPjTxaaNWEYGqerO7_IGjQX5X0r2fjerICY9b9rjklyFzuhN_khJwhG2VkJft4MDo-QX5f93ditqj7quuCgYFOncLvAb8SkZTh4XsiArYNigY8-v-lfNQtlVsMfOXE4KASmYd9uu_HLMYb4o09sRj5tKA6vLQIhn2tkHGp7gtfaODwd63vIWN3xeGjjaN2_E-GmEJj_Ku0Fwsi-UNJflxpmPF966hQf7oYmezQMANFxxJHzF09lAJCRNpXyuDUHAhd9heBwrTvGEhubm46ogA2D_LxoIjh-tPR_ieXUGzAgnrl2ddESsKTMyZTQqtxQiZN_rmGwu9z89yRLEQfFgsxOFIoBUAc0KJe6V3RuPIqOQakPI8DBiSAbNtiOBCnHVhV7Q-1BhAV1UoC-EvHu2b7hoytTgupQj-L6zxj_l4IyGmeigLm94wLNrEdRPsNIYfhRYk1EYkHPgwv9GUd1K0s04gRMnymtilsQTd&prev=RQ391BAA5050DFBB&p=13&pg=104)

* Italy
* IQVIA
* Brescia
* 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/ece073204e5290b9?ql=l&sig=1d7fb9dd713af66e194c4db96691e1b7b9ce2514&e=M9xNU4Hzym17OKJiXTK34rbx5U8RU_QUkEnqyhGj7rjFO8AtJEDuGzLfi2kblhA3ujZdsrUYsv1FIFc_5UexsW9Q8pEe6IQVA7wKVyRh-BNq8ZERtbobiQFe670Uslzi6pwc830Oz6Wd8Db-4W7giCak6RI6A5zdnMIBTSng58VPQrZ5X8ZHp1Cywtsabm9Kx5LWby0T6S6zcURBsj1AhBIPXbSIAPWYvSNZxRWG7NQ93LTke2U3iLINIYyKZm0P9FmkbkV68rnpCNgPTRmAEU5GF427BnrV4fAe-BmJve9OemJuQqpqwCXi_xlQEXxzwjqoc4jF7N10ujPSQMikmxCMKutSnZ7t2P8F-eZrDDcPFWIkLOiaUaTj-gyBd2vEc7rAs7yvaGn43iFNBVPk3zlLawH04MpGZwulpzPSg1hBkrj6Lm3O-Dz4B6FYJNbOzO0IrRvkorW1gohv59fCyTap2rIGDB6CmHwujnCTkZ1-PM3eZeMflgBJlKUyDVWLMJsr9di6OYSyQeY4VxNiZdh4dVCjTkC-dzBaU5rXx9PhK3hX6ye1m07-I52znzs_F38GJS1RJ3U_y3_9CW9B1H-DU03MXmEAdDHfebr_tRXMfMqTIPsDM48BVPlsOM9ag0gYB0zzh_1rt8zyxG-Cc__KrrBnyKiUApTUFtICVrmzt4eupwfTHAGv9yRXKkOZJKOqEGf3fehUtIfQKU7x4KOtOju0ZJSule53qnxVzQSY7YgqptvwDvJX6n4j8CD0jCEgOUt0cxm9WjPqNbv0Gh73G86Iu1sabKPXuFsgmgeTc4_1bUBk1QhbZjYuMvj6MVQP-I0Tup7yVxtXI2KO_gPhu4qPr975dw85IKpZ1cXZJc8e-jMQB0vfnaQlOg6U2fim_cGfk-fibzk3b4lMSeiOuRDux5cEw3_4BrX0IIvxKzBqdMJqD9DAMIsGjNbv_84h-spCa79dZQzh1Z6E7D_jkno5LJO6IvHPSS6uHEr_5F5Lt6G1mfA-LZOQ2Oan2BYm2PlaNp-k1EvOCJX_KE_9STEV-DlYTiLDKNSUCQy77Yzr4wiu6I_QmCXVF6E7QAfEiPZNNcRqScayiR9-ragtSNmN9wZInxTdSiWzp0TIvnt2TFRCFpv9CgsGEwPrU5ukaGQ7HgcG9VN0ZuWjLTA2U6CybokAR-pdlhP2dDvbfrPljQSLCIdiNSoleX_gkne4nwajl8OR7Xa0Ea_pEhZEIHOmplSeDJ8cu-UNKejJBF2YUA4lYCDfSShKc7fLNmHw5fbstkAcN3BP9TVMA-dNAOxxrAZf89SI3vsThFsLvEeNQepdIdabEz7py77r-glx-4p40GQeGPF1CTi1-vMzNjQjkKZmVJ5VDKxsph-_dsEG4UIEE6S53fm8osXQ_73y5eGqnzTxhDEqkf5_vtQxF8W1h8qab3cuGkJzLG12kF3gv7GYSdt3r0jhFcgnhpmg6VoKWpa4zcNWBygo8pg&prev=RQ391BAA5050DFBB&p=14&pg=104)

* Italy
* IQVIA
* Naples
* 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/ca7af69a48a29b45?ql=l&sig=dc2a4cda0e6a5b138a8da923de7d8af75ad73ba6&e=RMAbao_Xrv5HmTSUB3JpBxdwPkMr0ldrgK8jd2Hn4u73NxGMbWye1jwiMIdW6aCdDJGoVwwRtHQDSb1GjL0dgIakt9BWDEHgQiGQbbgA7nnf-5a4RiSPkmR8QfcJAUobKPr171YKGn5kd-uhShF5bEgzHdIFTUF-q92RLxIXIOJ5J_QjamOVdVjzm2sbd88A47g5iiJuEvuEhownGCMfiNlRwkLS8JoHXCMZQJ5hcQmdK3yOdMETVSWaCoswBWfiQMjaPSTho7UMxi4MnsiHLjiVS-rU10Yvk1XfOTgQ3H-5NKnF8cg-g06wRqRt-sPG12zWU3BqENkg6ew4cJeijSwy_SefMEH_Q9fwr8_n1cGEMK3KnQS6xaz3o3ucg3itIJZDJy5u7XPJX9VZkns-Le9Au19xATHO3-bH45zGWGYuCFlDaHVpBvc2zcZxcqBXQkuG-ZxwhMFZe-M6AeX04074T055kwgriHY7MvS4U7xusEqChkiIvrkpvnTuR38VZVfHz4PHv7Yfzuq9BKGjyfUciUor6rvk8JCACaLa0roU50ziiSZZOcT2Uv3ZAOn29AdNL3Sg3bRMIEmIYkQl9vaoOQVA513cPZRQYhhHBfkoGVmbwFmgWMwxtTkzlhv-k4zVPHoImLlxxHtXvP5tuOg-IaAI7mnxiARNbI4N_TO6RxFUTWJ4ozJPwHsu1WhfrpplZUH8xjq_R_qbhTPu7eqxWPKmE08GmLLsx6rnR7TQJlRGBnTra6kxAmxLUPsy5vQb3WDj_oQ6vJyZ_cCTJ980BUt9w2VDgMZ8Vk3Ah1YhVRgCC2oumeSQRa5U9IqyVhvb62oZbjRWylL2c1H6MYkVrmg54xgc96_h6XznvHfu0i90Ob_jYlyw-OlXi40hvHTviV6iUxXrMpSvhSL16PtkVf-XEVPUB-Mo2Zsorddp88jrm8Q-DZIusHGcVlXNzg5_q99ECtFEIZSKErTE0RtS-1XJ_B7zHKB7t37I8H6DumBR6Sey1A1wrv2xQWETQFmY7XhD7noMhR_6aCmiVR-frIAwEb2R36CyzXTqkLhcYAIBqSlNXOxkPS34Xx4N6fxSev_RxQzL_kDgC8T6QvgvUtfD4mq3qbEBUnJk5P3xTTkOLb9xZDqE22YsaD_8zGcsY_Mp_5qi9C51qxyAoKsFDysvcFCQiQQdYMzCxvstn3WNqHYnHF_gqwAQjGMCiVaOwSS1OD8M38Qf2gs4ax88Z890PF7rsh1jWqDh1Lib6JUdWe9I5o9nUq5WQSYoNoX3YO-k6fRVus8DmNfNLpQhHDXnMfDtMn1JZAqaaUVyQUiEh1Hg6EzJ-A63V8Co6da-75zDRHgFkT2orkVcsI-dkdqY26MlEMZTXIMMo1ixtJ55z6aoQLso9jwCwrvV4SSacLXJZodQOYnU3BA6DLJBPCjAIrkgFKIdl47kIUZpQA-1iOMhx2zHNFwXKXVN3O0q6kwfjEqOncZl0q1LvZV9&prev=RQ391BAA5050DFBB&p=15&pg=104)

* Italy
* IQVIA
* Bergamo
* 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/d2a2e22ff1bef3e3?ql=l&sig=cb34326ae954b29457dc649c2ac47aa199cfb3e0&e=quXlIzZD4sE7ZwEfibCBbbaQKFnYMOAHoFtqt5SlBu90j5MxTrwoi-0FySdfiPLENtP9mnW7OI1RUEst1PghjGdFwjjP_ANTUTPA9i3nbtoAAwuQitFukppRJo_Q1EkjkRlYpjEn_fYcUQhkIxc3RlHaV3j6z6gKWjLoqCh1hGBVNG5eBFlzIfYOvsouUBOYdVE_jnsfkgcKmNEeD6YEg3kA4higJ6juwN_Hwh4tpt6Q8wN5ErEDUXFYmIcuStvChtYZXF-ogFk58e9E0Vcr7LS5PbQ0K5X9cobP0J2mQr2UuS1PoT2JUv-1THYC4z3Kz2Ea6QVBC-mDxGcCsm4RZ7EFMhkxNA4AlPrZH2IGN9ZUEhKaR4omVoWgkWd8lqO3s8X7rDUmWORpNdH13jtFlD4hB5pcmtJ4ya8a_WYsz8cJnKtAJJcu6QUX96X5atQMgRfpa2a2FTSly2Wx4vhFimTSRvLVukCpT6rDI2QcA7HtTmVKU_ZEljzBsCtg35yA9I0aOMJ25d_qmurgaLwi2PXkmshB2f-qAMS9iNjlIAGomjwNxMHmUgjSB_QYIdW2kSu-S-q4O-nzipIkNPdq74huvCCkHXqlsFORbI_UDl7Hzd9DswdGUwgetx_Qe2wuA_UNiUyk2fGMil5eP-HVualQ407KB3LHgsxvvuxgGt7aA7YkjLKFW6FcXinIooUARMMCADceVnh83doVL8P4NJRhQhbBpQfhtadrHEte7K4BYyv_mjCRLm1EbED5aLsBkeFWX6-I6fDfcfpLvro85awCqmItAfQhOyrvNZVOp99CvohM2o4nBHKVUbVczydx9-O3duHEAAIxjD7rgi9z-_ooQJQ7nmcNW6zuc-XstLjvQlTh-KVct5w_qns6IXDIMm553BhBkHJd770bJepgbl5H05jWGpUPqrYfFJCKCp1TCGYKpfxsnRgdijau-x33mBq7WheO1FsTpc2yokYxCjD6Yn4BV064fr6TZjUNoiPV1eWKvrx_WTblm6mLdMj6j0rL92Ws1SnTNP8Xuz1emSAyXFhdS9AsHehEd2K0lvflNeXhTYQGkecqpxOIDd0CZSsKlr7R41izhH0pw99Z6PNlGVZYuR5Iq2xpUGxGWNZIg7V-gP21gXf3JayYOB5VT1ImYVc_oox2_82I_uFxN83E33MuDlTh4WgFMqO14V1qutr8R5s6VOmTa1Yb94-IoeJaV2EHJMuXq09yj-rt6RniN8GqVbZM54skswnqIL4awbpiLRW97pcDUQS3TQsvLJ9hSwq5L9HP2j-pdmLK2ay8-Zae3RAu-iD1Vm3cFAO1fVtTueSkFN2hgA_TyoEm6u57i-FBuBU1IC13y69yLlUUNhPzbXKRdsPmOzpcN3cTDIkll5F_vMpW4KxEtBRkTvzLBHKmOgxVhdor-WrR-1yVAFAFdvQ48O93SnMEzVSekFOOkDQTqAUtL5yIrBK2xDYM2O46DmRGqN51j1LcmmY&prev=RQ391BAA5050DFBB&p=16&pg=104)

* Italy
* IQVIA
* Venice
* 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/b2c7a45789e54c18?ql=l&sig=4847039717e2c7f7b96828d106d96b07bcc52296&e=s0UP7zqG1mpLrc0OWOef0Wv--I5gWhY2geVDZlsXImQmURZXoltLC5EUl4K4kxIe8GDnwu1x0E3qcTaTswHAz2-Uj3xIGuV-UTrnKWt7Y4hXcX0X4xdm1YzrymZXw4eAP7_myarxgC7EDcpdDEcjMTtqR2mY5WYugKX7u9Q3xshQrirXy91QsLCuU1yK1RPRvg-YwESFgXBQenuGSkaaWEREWGoCpM5It0Iu7F6a_YjJpzGui0ljfLq4H84EO42egkLZk1kL5kpX0w9F3MLXQaH4xPJGrUdL0-Fkolyi6jw_EZcBYHS4PWmMuaFsVOfx6y0scdh0Bjv0HbRriq-56WhRw01jXONzLfOVUYWeYIa_P1LZUEByT21TV7tyGuBOECxw5PbMxlImh6ak65s9x0xv4cweH6ErYwkyYrAJzo4E2MUa6svEQVWz7Ursonrb1uZ_9Cr0Cbe26PFOHOJbXbz-17IeHbPlDyXKJLaRMXmUWKSYQSP08Yd37_L_7d0psUoGLbemZ7hGJm2rF0F7NCqjF77WRpJWkLANceLSBVSJuxCct_-8a3c0fMKzJ89sjURAUVFnjaV7see7TarcNCpspiPg9xigieG_SCz0AleQCcwAme0FmEd5wjwEuCmiaHAWwwAcleBAz-_h6oDpmDqw2wwPyj2NXdA3Rqu9fCpkAxNo2MaxgTaJDJNVaUL-FDq4XhmbmdB2rN8fJN_j8L7e8Nms-aLgnkAhB8Z8694Tzbpa7BouzrJBSnUIhJp6ivGyyqf4pHsM9cnERwlayacOFheztNMUzpDT9aZgwg56YJuvcIk8W-W1VpoYqwCuit2BVtdmWMugxyLPWZFRrMCykyuomehWspKdrRVJeqVdsEknYP8NlNY_lUMvQThzf-So9wHFaJdr7eAYdhhig45WspCc-HNgrNaFdOYCA3qybe8oTwXLJmDMni8t6NoOzX81Whed2SyDp6htisBxgfm5dR44GfkEHPF2xeqmgGbF_rbhyT1hPcdL3j6aXKYV39p3YTB12innyeJHts5MOuC7uoCrTF9YBunHZAdaT0O5xRVzEYpCyjaYvaowQin5Ve_XIYYcfG6TpjBIgzRySqSY3WsYsueb9OHhiq99UKETnzYvCKTXjL_c9GqO-gCpGEzgoqXX3EoyREdoB74sBsgPENyKyMH22NvakNvZOWlTl77BYm_003Gck8UkOTA1zFKBwFYS1EfMkXSeN3XGSLZfBXsqJo7T9rxhH_dkZifVCWFGYRQVrF6NRxkxd4FpoFevAokIa-p9wo9ZjeBbStPrGQ6xB5EU1bLL0bQiUmV5kriNz_nRm-dZ7fpr98EaYoo4rnGK8gQ8YJaWx576xjh3aSoY-mcEB_PYEgOnJ-Dvy3kAIjiG5SIPQVQiRRmh233poKW3ifAEC6S4TrUTIhTkjaMkEYs99_kGrjBPgW7eDO7wfhdjxsWkynxw_MpWfZzm7WhJNd3Whxy39enAuLs&prev=RQ391BAA5050DFBB&p=17&pg=104)

* Italy
* IQVIA
* Modena
* 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/0c28b4238ccc1f86?ql=l&sig=d39b12a4278c2b2280203dc0f61b21665b8e2e5f&e=qD_AsQVanPcMiVR3niljQENt3gs-GfUWG6M8XqtXNJDSAgOhrS9tN118WouAR5X-mvsuOrDC_ltV9oyfoemLelN7vDonENBpWjMnFRSf34waVo88mN6zUt5gbsFds0YWuXVG-buB1VyWtWXix0Sy8uSECUmdDN6vGiVSPgTWZ2JWfzHp3LeN9IIX0gJfrBJLVtCYwU0hdT6wkZr29aUFwMZWdSePvVvfn7JJQrASvP0EMauhJN7LwDbyLdwXN6bBhwo7pGVRyHIFMe3o4USnUqE2QvWU_uEDYE7OYFgxX-8bSZ8x2G55gTbiZZcylVrOqgduORCWRz_fxux7PmFRjkqFUOzFH_ybnRlDnLbuoUxAIWlUOanfpQq28_524945pNG-8ojo_yxAJg6EtNBMm46TUG4rxUlxcoGMhAcab8hxNdx7JmVYhZNbh1xr9gtJaEnruVM24EaptDmEmt8SQLWjDgTafqvZEJChu5QqwTn_5SRLnMk0n_96SVgMDCBPs5VH7ujox3mxA2-SYgZWnT79eP4EywbXl8Uv82blJmGDxWx7zdrz6NcVNbPHfJCKZRgp_MgRgw08EbYSwNH1OO3C1RbUcMo7O9C1hmm0MKwc8vamQXDX-QDffkgRXw3Nz374YIitx7ii97OZ9-Jv9Tf2w3TPcI08OveTaLZQYQbdfnsLypVbiH9CpQgSJYvHyaJM2fOwT-CUezC_021nqITdk1B3jvn3x_0z_zz_-m7rOOinPH8AEyQNUZxuZdZZ6JflD-c_XYtu88OrSwRVdQaZ-m5OaxHMs_QhPSlIIadwtTnSeO3xeIESqHdzmMR1P8mGi-rvaMzNmd2i8dxq_yy3TOCKphh0ieaMUrZe78yO7QfJdjPTwJdx8ESA6S_qZLD7Yl67P8-tluibBRzMHBMLOzE2jZzvhoT5fQYmAiXRkZUm7CcrvDXmBGWr-VhqEWAkP2NFnvpg_J2Vdl9S2FZURnEc_WBGxXodYry5n_92N-bmdmq1vW9LJq3h0_aaSuV6HditVFS2KX1EmZPZ6XxtcTxe63Mh_Kk7_rZ8l89zJOMqb5UslNb6_3RTFri2C3RoNMtMlf0zgTLI198ZGKlQQbC85z-J1PxuBs0U1Rm4YwJC_EC5gZjbaMtzIvpUbqjDfWsQhL81JoLP60vGCajQznS9W18snnRjUB7stOQmAo3hn-oz0Usuxwbkyrj0nG5Q7Hl68lB4ZYK_-a5UqtdkEiRh9G_m_zOHQULY-EgAFwsiEo6p_bjMP8sdiiYZybLNmEvrPcH5kYSHDgFfqmaJqyUWOkRseTS2vOM0Ou5_IM3KL_o1R9xx3m409JR2pFVpTQjemGQCcmIbaWJagE86L24FEVBrHRBVyKS1THMVCcTr82Y04F-25Cb81a2CfWiyi_4ayaH8qEsO6g3sJn3L7ZwPB4oLlWlgJ-Ns8XoTAAG8ZtUJoyb4MsBWpW6U0gV2Aljib6f01vCMQ9WbLD6G&prev=RQ391BAA5050DFBB&p=18&pg=104)

* Italy
* IQVIA
* Vicenza
* 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/1ee1c004d5b59543?ql=l&sig=e7ac78ba72b2f5533590f999ae814b53f74ebd7f&e=7sbt258kAPX5eUKaRseN_6JGO0ZBh6utj5g20bos0XfZtlbRYF0l25PcYFXaGmt-N0fP7IsOTyoLClm_5MjYCpDwKq46EwahcBcN7a-jiVFG03tR9KynsKke7FGdP2TcfcmjUA-nQcoOogitnIpfGytxmLvX_N3mlksBEZaHEDAD4EAuZgaYz7IEw075nvtPe9TY6GLTsv47tY_43NtCr6r5WNDrK3M1n7TXkB6cvMaMtMlp87xVDU_VB8nZZssv_6Fh26lKTPwe3GuZmAEH8lPXFRMmdD1pdxPI0N4WrvoqKjdQaSldoSUitgK3BsTteSwZqsWDLGt5IXVd78yAYLnFuTNRPdUGdxF42P2TIUcFHqKU5LjHo7PmB65AvEqKaWsPL2GjDks0Qg6VM09icgOQMBhiliglmCf15OHYCZ5NVkMjAE66NU_5vcy8cGTPtyJEn6wkMSm-IK_WnwwXf-UajDiEyF44geqkTObKaRiSofGB7yDMp4CP8RdkJAk3i2Q_98MeU0zMQvzTITMZejkw9WjUU_14SyklwI5c2OeZx33GmZrwiKuwudvReNLRsgFfR08TaDa924P6t9RjunTmTq7CR-KajO7ft3nfaCfENSOteeN0LAaYv5xx4_FMlqTv64znamVvPk8JakAhkm5JlWR9ONZrmNzvdp2yR-hK354GFWpHT9E8e-1XD9k8b1DpcRmENj7WJTdGnbk6exytfnMXgB9ODI9DSoWldKn37aFPv1lntoEVaaQ53RWI7oX4W02RGnX60fCH4CBh2ts4YM7gKcIP8fwOPT4VJAay5mai9vHxBpQjVtVyRpeehXnrGwAq2znfh6ENkLYk67kDYb2ZQ8Tb0uQ_Jqps4LATBX0crLYaM6p-as4_hPeU1cpBLyKsFLlG8LvbJx8FyVPcLr2ZbyU-1WFDk38ElVYphhfNnCNp56P5PGGMomzch0Uok7AGK_fq6d-YED-2spOXebd14qFfSr1tg4AtHWgOznQt3dt8uAzhZdc-9L0M63p3DdVIvIUdKNvjsVcbZ4dT5v_n5wQcVHLlPsppTdnyRhqekEyLsgmP88xUIUgOyVZWbfmK8fCZeMt2SEI3oW4129nsCmyTzDVT7zueVQFH2KYsnWD77TbFKns4mmhiUr1916aZPZ8C2Mt1jvYloxbUDcdQ5VDeu7SA7zbKC82Y67pvBBvyPw9JqmglJPJ1EUGUDsxtmo1HStFSjELn3j0uuRrU_t2mDpFhpIMx3B6zK1Pr1cq0nhxar1r4CILEZvWQG8o8EaTUU1LNZQqf9cpB4WTPZWfFedQ9at8w80trjKCkKQe_wg6qmMHwI9SWMEF2la4yMxd1Dh-VR17-H42pu66TSTNE-N9VN-8V34JRnsUYXfF3cFvaRlnZmCCs_9AJk-S8RU5hGhEZ2xV7EFkyGMOivm83J72Ph_JE7QQ5T2OH0o48jzyNtQMn4BMAUvICqx9OELLatAZoBSFx8g&prev=RQ391BAA5050DFBB&p=19&pg=104)

* Italy
* IQVIA
* Parma
* 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/f9ad3002501dedaa?ql=l&sig=65686804e6144c38df313e5b42d334310dd4fe86&e=O56f5JYsx4iHO8LWpRyKOmCBGAH9MsLFTLhZqmtq3_710M5kIxEVUKFChoH3ednfA5wWH0ABBbDA6lEKDfWkET7_kWyNUxxZOK2_wJbGuwILcySaKI9X9lOALjGP_da3_Lgwt0BJtq3DjyPptTuCwW_CKGWui2p_8loJ8rcrYO-MDNFoydb2LJXuI2uV9gVWBHaUBxRfXAQPGRZ81U1oG2EBF7mliG7FK7d-tVpYOZ4WKCulQ7ODVyuTUpyDPDZVOEo_QuyVCLonzUOf_akFCz3egKzFFwYR4p7mNk9hoVYzt_altNQ-Y2oHnsxK_7qEcU3_--wENHhyE04x6Ag2GbuM-zEwjp8kaVyWlG7NNKGEw76VcTjcyg0jomemZy23wBcLSIcBfY-UvZ6ADBowxW87llfhFP0QcWuaXVl-MRpwJ4HK62dBKiOGT9FvCHcOK7pCF-JV5yOHgjM7N_P_cMcEDMZSne1cQPK7qjzW4qXKOlARN9nKwAxEfM9j0kBy6j4_eqXFAfnNkg4lnqwUgTFO6T1wKDkEUY0U3idMDWimj2ECf6XbY8NWncjYa6ayEd1vyO03h2-M24eLPuO0lMJ8VRYoEUKcfxNEegVzs1TM9_NGFsKiiPA042Njamaw-2YOIPyLMV0c6I0ra1ZABo9_Xi9hzIvWS9y6_pHENc6I5fS3TVWnO_hcwiUbzGCexYIESG90wp7dd5Madj4SZiLAp8vEg3lyvIZmS8AWOfj48-Zv8km-pyioSA_PcOx3KWStECYHs3UotzpX-wgX20_pB4i1vSabr2tSUGiRQIwrAUsROtJ21rikJ5x35dEopn1arLAgVxJIFbd5YsD-sDXlVEt0GC7RhLRR65YXYkdQZ8WFIltMYCU0L5hFjQpUrpsojjzX55NWiXEuC2s95UNPWjRVACvC3-TikdEF8htD_zE_6zU1MmwW5fR84VsW1vTxX3nnjGxWbiOB-15s-jHz6Yor7_PldRxoXSQSJzGoagrYV4Kletpz_CgpMVjTVUnn-s_zhIFXwvzu7UOSH-tHLKP335f_0i4ihI1--zblPU8udUTKuGn5hd5yeSGV6tgORoEqZs5gerjDdJPlwcyWkG8hIqg0DweXP6wxVg2_ZDDJfwUHuIhLopIqqSoDEAhE73IN8yrVGyUegBMT0AQrwCotM7vehTw6I0b1k9kKHDBVduRZtUjLHxYhzphd4ekJ468mknlSSrd816RQ7l0xgJDTod9ocq9L_EWHcfZBLoOBdoHWMvAQgLFnkXJ-PA46cZhdeC8-5AjddmdJVBdawXSOU2UducV4XM4dbBooDrD64vSTKympt6cmUtBDVc6sKHtkDGEgQQdTMlrpMaPjpbFd9q5MGsONOU-dJ_f0l4wJysbnabfG5xk13QAuOBPBm4fX1IVrX5CZG_tPlJ7FooXsbNOU7Cg6vzZUXl-KvB5oItN1Js3TdXM75dscCty4WTZDRlUzKGyoIOyWeEXO&prev=RQ391BAA5050DFBB&p=20&pg=104)

* Italy
* IQVIA
* Treviso
* 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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