Description
Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, 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 documents, ensure contracts are fully executed, and establish project timelines.
Key responsibilities include:
- Serving as a Single Point of Contact (SPOC) for feasibility, site activation, and maintenance activities in assigned studies
- Reviewing documents for completeness, consistency, and accuracy
- Preparing site documents and distributing them to sites and internal project team members
- Updating and maintaining internal systems, databases, tracking tools, timelines, and project plans
- Reviewing, tracking, and following up on the progress of required documents
You will require:
- A Bachelor's Degree in Life Sciences or a related field
- 1-3 years of clinical research or other relevant experience, or equivalent combination of education, training, and experience
- 3 years of experience in a healthcare environment or equivalent combination of education, training, and experience
Benefits include a range of health and welfare options, and the potential base pay range for this role is $49,200.00 - $123,000.00 per year.