Offer summary
Qualifications:
BA/BS in Communications or related field, Minimum 2 years experience in biotechnology, pharmaceutical, or CRO, Knowledge of clinical practice and regulations, Fluency in English; Spanish or French is a plus, Experience as study coordinator or managing patient advocacy groups.
Key responsabilities:
- Develop recruitment strategy in collaboration with Patient Recruitment Team
- Train project teams on recruitment strategies
- Monitor subject enrollment and suggest improvements
- Collaborate with regulatory teams for material approval
- Ensure project documentation is filed appropriately