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Clinical Study Contracts Specialist
1 month ago
As a Clinical Study Contracts Specialist at Pharmiweb, you will be responsible for coordinating, preparing, and executing clinical study contracts and amendments. You will work closely with clinical teams to ensure the successful execution of clinical trials.
Key Responsibilities:- Coordinate and prepare clinical study contracts and amendments
- Work closely with clinical teams to ensure successful execution of clinical trials
- Negotiate financial and legal conditions
- Track and oversee contract status at the local level
- Develop and standardize local contract templates and MSAs
- Minimum 2 years of experience in clinical study contracts at pharma or CRO environment
- Excellent communication skills in English, Dutch is an asset
- Preferred soft skills: negotiation capacity, proactivity, effective prioritization & organization, and problem-solving mindset
- Competitive salary
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
At Pharmiweb, we value diversity, inclusion, and belonging. We are committed to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know.