Descrizione dell'offerta
Job Description Join Our Team and Shape the Future of Clinical Research! At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist, 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. In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.
Key Responsibilities:
Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials. Ensure compliance with SOPs, regulatory guidelines, and contractual obligations. Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution. Identify and elevate contractual issues to management as needed. Support the internal review, revision, and approval process of contracts before forwarding them to external parties. Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution. Maintain electronic and paper contract files, ensuring accuracy and accessibility. Assist in the continuous improvement of departmental processes and procedures. Provide regular status updates to management and study teams. Required Qualifications:
Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable. Fortrea may consider equivalent relevant experience in lieu of educational requirements. 2-4 years of experience in contract negotiation, clinical research, or a related field. Strong understanding of ICH GCP guidelines and clinical research processes. Excellent negotiation, communication, and organizational skills. Ability to work independently and manage multiple priorities in a fast-paced environment. Proficiency in Microsoft Office and contract tracking systems. What We Offer:
Competitive salary and performance-based incentives. Flexible work arrangements (remote/hybrid options). Professional growth opportunities in a collaborative and innovative environment. The opportunity to work on cutting-edge clinical research projects. The base salary range for this role is €35,000 - €51,00 gross per year, which may vary as per working schedule (full or part-time). The final offer will be determined based on objective and job-related criteria such as experience, qualifications, and scope of responsibilities, in line with our internal job classification framework and the applicable collective labour agreement (CCNL). This role may also be eligible for additional compensation, such as bonus and benefits, in accordance with company policies. At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job - it's a journey of making the exceptional possible, every day.
#J-18808-Ljbffr
Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials. Ensure compliance with SOPs, regulatory guidelines, and contractual obligations. Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution. Identify and elevate contractual issues to management as needed. Support the internal review, revision, and approval process of contracts before forwarding them to external parties. Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution. Maintain electronic and paper contract files, ensuring accuracy and accessibility. Assist in the continuous improvement of departmental processes and procedures. Provide regular status updates to management and study teams. Required Qualifications:
Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable. Fortrea may consider equivalent relevant experience in lieu of educational requirements. 2-4 years of experience in contract negotiation, clinical research, or a related field. Strong understanding of ICH GCP guidelines and clinical research processes. Excellent negotiation, communication, and organizational skills. Ability to work independently and manage multiple priorities in a fast-paced environment. Proficiency in Microsoft Office and contract tracking systems. What We Offer:
Competitive salary and performance-based incentives. Flexible work arrangements (remote/hybrid options). Professional growth opportunities in a collaborative and innovative environment. The opportunity to work on cutting-edge clinical research projects. The base salary range for this role is €35,000 - €51,00 gross per year, which may vary as per working schedule (full or part-time). The final offer will be determined based on objective and job-related criteria such as experience, qualifications, and scope of responsibilities, in line with our internal job classification framework and the applicable collective labour agreement (CCNL). This role may also be eligible for additional compensation, such as bonus and benefits, in accordance with company policies. At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job - it's a journey of making the exceptional possible, every day.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
Ricevi annunci simili
Inserisci la tua email: ti avvisiamo quando escono nuovi annunci corrispondenti.
✅ Controlla la tua email e clicca il link per confermare l'alert.
Nessun account necessario. Disiscrizione con un clic dall'email.