Description
At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading sponsor's team while benefiting from the global expertise, career development and support of IQVIA.
As an Associate Clinical Operations Manager, you will play a critical role in accelerating clinical trial start-up by leading the negotiation, preparation and execution of site agreements and associated legal documents.
Responsibilities
- Negotiate clinical trial contracts with research sites, ensuring agreements are completed on time and meet quality and compliance requirements.
- Manage contract changes and additional agreements while balancing business needs and regulatory requirements.
- Support contract planning and study start-up activities for assigned sponsors, studies, and programs.
- Help develop investigator grants, site budgets, contracting plans, and proposal documents.
- Prepare and negotiate contract terms, payment schedules, and budget templates based on project and sponsor needs.
- Work closely with sponsors, stakeholders, and regional study start-up teams to achieve project goals and timelines.
- Provide contract-related guidance and support to study teams on operational and financial matters.
- Gather and share contract and market information to support study planning and decision-making.
- Monitor contract activities to ensure timelines, milestones, and financial goals are met.
Qualifications:
- Bachelor’s degree or equivalent.
- 3-5 years of experience in clinical research contract management or a similar role.
- Familiarity with clinical trial processes, regulatory requirements, and contract lifecycle management.
- Strong analytical, organisational, and communication skills.
The potential base pay range for this role, when annualized, is €41,000.00 - €61,400.00.