Overview
Employer Industry: Clinical Research
Why consider this job opportunity
- Opportunity for career advancement and growth within the organization
- Flexible work environment, as the position can be based anywhere in the United States
- Work with a dynamic, global team dedicated to changing lives through medical science
- Engage in meaningful work that contributes to the development of new medicines
- Supportive company culture that values staff and partners
What to Expect (Job Responsibilities)
- Facilitate negotiations of site agreements and budgets to ensure alignment with the site activation plan
- Customize and prepare country- and site-specific agreements, organizing their translations
- Track the status of site agreement and budget negotiations
- Prepare executable versions of site agreements and budgets, coordinating the signature process
- File executed site agreements in the Trial Master File and update all concerned functions on the site contracting process
What is Required (Qualifications)
- College or university degree or an equivalent combination of education, training, and experience, with a minimum of 2 years' relevant experience
- Minimum 1 year of experience in the clinical research industry in the United States
- Previous experience with negotiating site budgets
- Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus
How to Stand Out (Preferred Qualifications)
- Experience working in a fast-paced environment related to clinical trials or research
- Familiarity with regulatory guidelines and compliance in clinical research
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