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Director, GCP & GLP Quality Assurance – Clinical-Stage Biotech – Fully Remote
143457
Posted:
23rd
April 2024
- 190000 USD - 220000 USD
- Boston, United States
- Permanent
Director, GCP & GLP Quality Assurance – Clinical-Stage Biotech – Fully Remote
About Us
Join a dynamic and rapidly expanding clinical-stage Biotech, with an excellent cash runway and support us in our goal to commercialize our revolutionary platform and support patients globally across multiple therapeutic areas.
This is an excellent opportunity to take ownership of the GCP QA activities within our business, leading GCP and GLP oversight of studies and drive GCP QA strategy.
Why Us?
Are you an experienced GCP QA professional with a proven track record of ensuring compliance with GCP and GLP, supporting clinical development programs and managing CROS and Regulatory Authority relationships? We want to hear from you.
Role Responsibilities:
As the Director, GCP & GLP Quality Assurance, you will be responsible for:
As the Director, GCP & GLP Quality Assurance, enjoy a competitive salary, bonus, long-term incentives including stock and fully remote-work
How to Contact Us:
For more details, contact Guled Samatar at Meet - call 646 582 3675 or email guled@peoplewithchemistry.com for a confidential discussion.
About Us
Join a dynamic and rapidly expanding clinical-stage Biotech, with an excellent cash runway and support us in our goal to commercialize our revolutionary platform and support patients globally across multiple therapeutic areas.
This is an excellent opportunity to take ownership of the GCP QA activities within our business, leading GCP and GLP oversight of studies and drive GCP QA strategy.
Why Us?
- Fully Remote: Work from anywhere in the US
- Package: Competitive salary with a substantial bonus and stock options
- Career Development: Thrive in a collaborative environment fostering your professional growth
- Company Culture: Excellent staff-retention and culture make us a great workplace
Are you an experienced GCP QA professional with a proven track record of ensuring compliance with GCP and GLP, supporting clinical development programs and managing CROS and Regulatory Authority relationships? We want to hear from you.
Role Responsibilities:
As the Director, GCP & GLP Quality Assurance, you will be responsible for:
- Ensure compliance with GCP, GLP and regulatory guidelines
- Lead all aspects of Clinical QA
- Manage relationships with vendors including CROs
- Implement GCP Audit Program
- Prepare for and host Regulatory Authority inspections
- 10+ years in GCP QA
- Experience within GLP QA
- Background in Pharma / Biotech
- Life-science degree or equivalent
As the Director, GCP & GLP Quality Assurance, enjoy a competitive salary, bonus, long-term incentives including stock and fully remote-work
How to Contact Us:
For more details, contact Guled Samatar at Meet - call 646 582 3675 or email guled@peoplewithchemistry.com for a confidential discussion.
Guled Samatar
Sector Leader