Sponsor Dedicated Site Budget
Vor 14 Stunden
Zürich, Zurich, Schweiz
Fortrea
Vollzeit
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ppbJoin Our Team and Shape the Future of Clinical Research /bbr/At bFortrea /b, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Contract Specialist (
location:
Switzerland; Home-Based), you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.br/In this role, you will be part of our FSP team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications. /p h3Key Responsibilities /h3 ul liPrepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials. /li liEnsure compliance with SOPs, regulatory guidelines, and contractual obligations. /li liTrack, update, and maintain contract status in relevant systems, ensuring transparency and timely execution. /li liIdentify and escalate contractual issues to management as needed. /li liSupport the internal review, revision, and approval process of contracts before forwarding them to external parties. /li liCollaborate with clinical study teams, legal, and project management to ensure seamless contract execution. /li liMaintain electronic and paper contract files, ensuring accuracy and accessibility. /li liAssist in the continuous improvement of departmental processes and procedures. /li liProvide regular status updates to management and study teams. /li /ul h3Required Qualifications /h3 ul liBachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable. /li liFortrea may consider equivalent relevant experience in lieu of educational requirements. /li li2-4 years of experience in contract negotiation, clinical research, or a related field. /li liStrong understanding of ICH GCP guidelines and clinical research processes. /li liExcellent negotiation, communication, and organizational skills. /li liAbility to work independently and manage multiple priorities in a fast-paced environment. /li liProficiency in Microsoft Office and contract tracking systems. /li liFluent in German and in English /li /ul h3What
We Offer
/h3 ul liCompetitive salary and performance-based incentives. /li liFlexible work arrangements /li liProfessional growth opportunities in a collaborative and innovative environment. /li liThe opportunity to work on cutting-edge clinical research projects. /li /ul h3Ready to Make an Impact? /h3 pTake the next step in your career and join us in driving innovation in clinical research. /p /p
location:
Switzerland; Home-Based), you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.br/In this role, you will be part of our FSP team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications. /p h3Key Responsibilities /h3 ul liPrepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials. /li liEnsure compliance with SOPs, regulatory guidelines, and contractual obligations. /li liTrack, update, and maintain contract status in relevant systems, ensuring transparency and timely execution. /li liIdentify and escalate contractual issues to management as needed. /li liSupport the internal review, revision, and approval process of contracts before forwarding them to external parties. /li liCollaborate with clinical study teams, legal, and project management to ensure seamless contract execution. /li liMaintain electronic and paper contract files, ensuring accuracy and accessibility. /li liAssist in the continuous improvement of departmental processes and procedures. /li liProvide regular status updates to management and study teams. /li /ul h3Required Qualifications /h3 ul liBachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable. /li liFortrea may consider equivalent relevant experience in lieu of educational requirements. /li li2-4 years of experience in contract negotiation, clinical research, or a related field. /li liStrong understanding of ICH GCP guidelines and clinical research processes. /li liExcellent negotiation, communication, and organizational skills. /li liAbility to work independently and manage multiple priorities in a fast-paced environment. /li liProficiency in Microsoft Office and contract tracking systems. /li liFluent in German and in English /li /ul h3What
We Offer
/h3 ul liCompetitive salary and performance-based incentives. /li liFlexible work arrangements /li liProfessional growth opportunities in a collaborative and innovative environment. /li liThe opportunity to work on cutting-edge clinical research projects. /li /ul h3Ready to Make an Impact? /h3 pTake the next step in your career and join us in driving innovation in clinical research. /p /p