Description
We are seeking experienced CRA 2s to lead and support our Full Service Outsourcing team. The role involves utilizing clinical judgement to provide high-standard care for participants in clinical trials, responding to emergency situations, and ensuring compliance with regulatory requirements.
Responsibilities
- Conduct routine monitoring and close-out of clinical sites
- Maintain study files and ensure proper materials and instructions for study staff
- Verify informed consent procedures and protocol requirements
- Ensure data integrity and monitor for missing or implausible data
- Manage registry and undertake feasibility work
- Complete Serious Adverse Event (SAE) reporting and follow-up
- Perform CRF review and query generation
- Assist with training of new employees
- Coordinate clinical projects as Local Project Coordinator
Requirements
- University or college degree, or certification in a related allied health profession
- 6 months-2 years of Clinical Monitoring experience
- Ability to work in a fast-paced, changing environment with strong teamwork and people skills
- Comfortable with technology-based data collection
What do you get?
- Comprehensive benefits, including medical, dental, vision, life, and disability insurance
- 401(K) and paid time off (PTO)
- Employee recognition awards and multiple ERG's
- Target pay range: $105-125K