Senior Site Contracts Associate, IQVIA Biotech
$62,800–$157,100 year
On-siteDurham, North Carolina, United States
Job Summary
Develop global contracting strategies and coordinate investigator grants, estimates, and proposal text for selected sponsors and multi-protocol programs. Draft contract and payment language, maintain contracting systems and training materials, and collaborate with sponsors, stakeholders, and regional units to deliver project scope while ensuring compliance. Provide specialist legal, operational, and financial support to study teams to facilitate clinical trial initiation and maintenance, review core scientific and administrative documentation, and contribute contracting intelligence. Ensure adherence to project timelines, financial goals, and quality standards by reporting performance metrics and working with Quality Management. Mentor colleagues on training materials and deliverables.
Required Qualifications
- Bachelor's Degree Related field
- 3-5-year relevant sponsor or clinical research organization clinical site contracting experience
- demonstrable global and/or regional experience acting as a contract negotiator
- Equivalent combination of education, training and experience
- Good negotiating and communication skills with ability to challenge
- Strong legal, financial and/or technical writing skills
- Strong understanding of regulated clinical trial environment
- knowledge of drug development process
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Knowledge of applicable regulatory requirements, SOPs and company's Corporate Standards
- Good understanding of clinical trial contract management
- Ability to develop and suggest alternate contracting language, terms, and financial options
- sponsor facing experience
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