IQVIA, a global leader in clinical research and healthcare solutions, is expanding its Contracts & Study Start-Up team. The company is currently hiring for two exciting roles:
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- Contracts Analyst
- SSO Contracting Specialist
Both roles provide an opportunity to work on high-impact projects in pharma and clinical research, ensuring compliance, efficiency, and innovation in healthcare contracting processes.
Role 1: Contracts Analyst
Key Responsibilities
- Review, draft, and manage contracts related to pharma and clinical projects.
- Collaborate with internal teams to prepare accurate proposals and agreements.
- Ensure compliance with regulatory standards and company policies.
- Support negotiations and maintain documentation for audit readiness.
- Contribute to process improvements and workflow efficiency.
Required Qualifications
- 1–2 years of experience in contracts or proposals (preferably in pharma/clinical industry).
- Educational background in B. Pharma, M. Pharma, Pharm-D, MSc, or BSc.
- Strong communication, organizational, and analytical skills.
- Ability to work effectively in a fast-paced, office-based environment.
Role 2: SSO Contracting Specialist
Key Responsibilities
- Support country SSU (Study Start-Up) strategy in collaboration with SSO Study Start-Up Managers and Team Leads.
- Coordinate, prepare, and execute clinical study contracts (PI, site, institution, MSA, local vendors, etc.) and amendments.
- Track and oversee contract status including dispatch and return of contracts.
- Negotiate financial and legal conditions; escalate issues as required.
- Act as the single point of contact for local Legal and ERC regarding patient reimbursement and related topics.
- Develop and standardize local contract templates and MSAs.
- Ensure adherence to ICH/GCP, IRB/IEC, SOP, and Health Authority regulations.
- Implement innovative and efficient contracting processes aligned with client strategy.
Required Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field (B.Pharm, M.Pharm, Pharm-D, MSc, or BSc).
- Prior experience in clinical contracts, SSU, or regulatory operations preferred.
- Strong negotiation, coordination, and stakeholder management skills.
- Knowledge of ICH/GCP and regulatory requirements.
Benefits of Joining IQVIA
- Opportunity to work with a global leader in healthcare and life sciences.
- Exposure to diverse pharma and clinical research projects.
- Career growth opportunities in contracts, regulatory, and study start-up operations.
- Collaborative, innovation-driven work culture.
How to Apply
Interested candidates can share their updated resumes directly at:
📧 foram.chheda@iqvia.com
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