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Principal Site Contracts Associate
ParexelPrincipal Site Contracts Associate handling site agreements and managing contractual processes in clinical development. Engaging with clinical trial sites and ensuring compliance with local regulations and guidelines.
About the role
Key responsibilities & impact- Draft, review and negotiate site agreements including clinical study agreements, service agreements, and team member agreements
- Provide context to comments received from sites based on legal and business framework
- Manage the contract execution process
- Develop and maintain positive relationships with clinical trial sites
- Track and report on the statuses of site contracting activities
Requirements
What you’ll need- 8+ years of experience in site contracting or a related field within the CRO industry
- Strong negotiation and organizational skills
- Proficient in Microsoft Office Products specifically, Excel, Word, and PowerPoint
- Ability to mentor and motivate junior staff
- Fluent in written and spoken English; command of additional languages is beneficial
Benefits
Comp & perks- Health insurance
- Retirement plans
- Professional development
- Paid time off
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Site Agreement DraftingClinical Study Agreement ReviewService Agreement NegotiationContract Execution ManagementStatus Tracking and Reporting
Soft Skills
Relationship ManagementMotivational Skills