Cra2/scra

THE ROLE:

- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with Good Clinical Practice
- Administer protocol and related study training to assigned sites
- Manage the progress of assigned studies by tracking regulatory submissions and approvals.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
- Collaborate and liaise with study team members for project execution support as appropriate.

**REQUIREMENTS**:

- Bachelor's Degree in scientific discipline or health care preferred.
- A minimum of 2 years' on-site monitoring experience.
- Good therapeutic and protocol knowledge as provided in company training.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Clintec, an IQVIA company, is an innovative global functional services provider with a depth of expertise in oncology and rare diseases.