Job Summary
A clinical study company is searching for a person to fill their position for a Telecommuting GSPV Submission Specialist I.
Core Responsibilities Include:
- Filing documents according to project specific requirements
- Providing Sponsor with expedited and periodic safety report submission status updates
- Assisting with the tracking of safety submissions
Applicants must meet the following qualifications:
- Excellent communication, presentation, interpersonal skills, both written and spoken
- Nominal clinical research or equivalent combination of education and experience
- Associate/foundation degree required
- Proficiency in Microsoft Office Suite
- Good knowledge of ICH guidelines and regulations relating to Safety and Pharmacovigilance
- Strong organizational and documentation skills