Description
IQVIA is seeking a Clinical Research Contract Specialist to join their team.
The successful candidate will be responsible for coordinating the development of investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process.
Key responsibilities include:
- Developing contract language and budget templates as required
- Utilizing and maintaining contracting systems, tools, processes, and training materials for selected sponsors, studies, or multi-protocol programs
- Ensuring collaboration with sponsors, stakeholders, and RSU regions and countries to successfully deliver the agreed project scope
- Providing specialist legal, operational, and financial contracting support to Study Teams
- Ensuring overall contracting efficiency and adherence to project timelines and financial goals
- Reporting contracting performance metrics and out-of-scope contracting activities as required
- Working with Quality Management to ensure appropriate contract management and quality standards
- Mentoring and coaching colleagues as required
The ideal candidate will have:
- A Bachelor's Degree in a related field or 2 years of relevant sponsor or clinical research organization clinical site contracting experience
- Good negotiating and communication skills with the ability to challenge
- Experience in negotiating clinical trials agreements with sites in the Czech Republic
- Strong understanding of the regulated clinical trial environment and knowledge of the drug development process
- Good understanding of clinical trial contract management
- Fluent in English
IQVIA offers a range of benefits and opportunities for professional growth and development.