A recognized pharma company in Massachusetts is looking to add a new Clinical Trial Specialist to play a critical role in supporting clinical trial programs by ensuring proper coordination and adherence to regulations.
Responsibilities:
- Performing study feasibility assessments
- Developing and reviewing study documents and site documents
- Managing regulatory document processes
- Coordinating investigational product releases
- Managing and tracking study-specific payments
Qualifications:
- Bachelor's Degree
- Knowledge of Study Phases in Clinical Development
- Familiarity with ICH Good Clinical Practice guidelines
- Issue identification and resolution abilities
- Effective verbal and written communication skills
- Relationship-building skills with management and peers
Desired Skills:
- Master's Degree
- Previous experience in Clinical Trial Coordination
