Job Summary
A biopharmaceutical services organization is filling a position for a Remote Clinical Regulatory Affairs Senior Consultant.
Individual must be able to fulfill the following responsibilities:
- Leads other special projects
- Participates in and/or otherwise supports development and implementation of new or updated PDR
- Completes other routine and ad hoc analysis and reporting
Applicants must meet the following qualifications:
- May require travel to client's US location
- Strong business acumen
- Experience in regulatory affairs
- Average of 10+ years' relevant clinical experience in regulatory affairs
- Bachelors Degree required
