Description
Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, standard operating procedures (SOPs), and project requirements at the regional or country level.
You will prepare and manage site documentation, review and negotiate site documents and contracts with sites and sponsors, maintain and report on site performance metrics, serve as the primary point of contact for investigative sites, track completion of appropriate documents for sites, ensure contracts are fully executed, and establish project timelines.
Key responsibilities:
- Act as Single Point of Contact (SPOC) for feasibility, site activation, and some maintenance activities in assigned studies
- Prepare site documents, reviewing for completeness and accuracy
- Inform team members of completion of regulatory, contractual, and other documents for individual sites
- Distribute completed documents to sites and internal project team members
- Update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information
- Review, track, and follow up on the progress, approval, and execution of required documents
Requirements:
- Bachelor's degree in Life Sciences or a related field
- 1-3 years of experience in clinical research or a related field
- 3 years of experience in a healthcare environment
We offer a range of health and wellness benefits, and the potential base pay range for this role is $61,400.00 - $102,400.00 per year.