About the Role
We are seeking an experienced Clinical Site Contracts Specialist to join a global Clinical Research Organization (CRO), working directly with a leading sponsor on complex, high-impact clinical trials. This is a remote-based position requiring a high level of autonomy, strategic thinking, and contract negotiation expertise.
You will be responsible for drafting, reviewing, and negotiating Clinical Trial Agreements (CTAs) and budgets with clinical trial sites across the Nordic region. This role is ideal for someone who thrives in a fast-paced, global environment and can independently manage contract-related challenges before they escalate.
Key Responsibilities
- Draft, negotiate, and finalize Clinical Trial Agreements and associated budgets with clinical sites.
- Identify and proactively manage contract risks and challenges with minimal oversight.
- Collaborate with internal teams and external stakeholders to ensure timely contract execution.
- Ensure compliance with applicable laws, regulations, and sponsor requirements.
- Maintain accurate documentation and contribute to process improvements.
What We’re Looking For
- 6–7+ years of experience in clinical contracts and budgets, ideally within a CRO or pharmaceutical company.
- Proven ability to manage complex studies and work independently.
- Strong expertise in drafting and negotiating CTAs in a global clinical trial setting.
- Deep understanding of regulatory and legal frameworks related to clinical research.
- Excellent communication, problem-solving, and stakeholder management skills.
- Fluency in English; proficiency in a Nordic language is a plus.