The Senior Clinical Trial Coordinator will support the clinical project team during all stages of a clinical study, carrying out day-to-day study activities, developing and implementing study procedures, and managing clinical studies. The Sr. CTC will be responsible for tracking, review, and collection of study-specific documents, managing device accountability, and ensuring data quality.
Requirements
- BA/BS or equivalent experience in scientific or healthcare disciplines
- Minimum of two (2) or more years experience in clinical research, with medical device and/or pharmaceutical trials
- Strong computer skills with proficiency with MS Windows-based applications
- Working knowledge of ICH Good Clinical Practice guidelines
- Excellent communication skills (oral and written)
- Strong organizational skills with attention to details
- Ability to build and maintain positive relationships with management and peers
- Ability to work independently and manage multiple tasks in a fast-paced environment
- Ability to work effectively on cross-functional teams
- Valid driver’s license
- Ability to travel domestically up to 10%
Benefits
- Competitive salaries
- Annual bonus
- 401(k) with company match
- Comprehensive medical, dental, vision coverage
- 24/7 Employee Assistance Program
- Free live and on-demand Wellbeing Programs
- Generous Paid Vacation and Sick Time
- Paid Parental Leave and Adoption Assistance
- 12 Paid Holidays
- On-Site Child Daycare
- Café
- Fitness Center
