Clinical Contracts Associate

03 ott - Italia
Advanced Clinical

pbContract: /b Initial 12 months, with potential for rolling 12-month extensions /p pWe are looking for a Clinical Contracts Associate to manage the preparation, negotiation and execution of clinical trial contracts and budgets across EMEA. You will work directly with research sites and collaborate with legal, compliance and clinical teams to resolve contractual issues and keep studies moving forward. /p h3Responsibilities /h3 ul liPrepare, review and negotiate clinical site agreements, work orders, amendments and change orders. /li liAdapt study budget templates to country and site requirements, ensuring budgets reflect protocol activities and applicable policies. /li liAssess contractual risk and propose practical solutions. /li liNegotiate terms covering indemnification, intellectual property, confidentiality and compensation. /li liReview country and site changes to informed consent wording concerning injury, data privacy and compensation.



/li liManage your workload independently and provide guidance to less experienced colleagues when needed. /li /ul h3Requirements /h3 ul liAt least four years of relevant experience in clinical research, pharmaceuticals, medical devices or a clinical environment. /li liStrong hands-on experience with clinical trial contracts and site budget negotiation. /li liAbility to work independently, manage competing deadlines and handle confidential information. /li liStrong written and spoken English, with the confidence to negotiate directly with research sites. /li liGood working knowledge of Microsoft Word and Excel. /li liA degree or equivalent relevant experience. /li /ul pExperience with cardiac, vascular or neuromodulation studies would be an advantage, as would a strong understanding of clinical study protocols. /p #J-18808-Ljbffr

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