What are the responsibilities and job description for the Associate Director, Clinical Quality Assurance position at Meet?
Associate Director, Clinical Quality – Global Biotech in Maryland
About Us
Join a leading global biotech business renowned for groundbreaking therapies that address critical unmet medical needs. We are seeking an experienced Sr. GCP Quality Professional to become an integral part of our Quality team and drive excellence in clinical quality operations.
Why Us?
- Patient-Centric: Contribute to life-changing therapies that make a real difference
- Competitive Compensation: Attractive salary, substantial bonus, stock options and benefits
- Career Growth: Thrive in an environment that prioritizes professional development and advancement
- Great Culture: Industry-leading staff retention and a collaborative, supportive workplace
Who We Are Looking For
We are looking for an experienced Clinical Quality professional with a proven track record in GCP QA audit programs, managing clinical quality systems, and overseeing vendor relationships, including CROs.
Role Responsibilities:
As the Associate Director, Clinical Quality Assurance, you will:
- Develop and implement GCP QA audit program
- Manage the Clinical Quality Management System
- Oversee vendor-conducted audits, including Site Audits
- Lead inspection-readiness activities
- Collaborate closely with Clinical Operations and cross-functional teams
Desired Skills:
- 7 years’ experience in Clinical Quality within Pharma / Biotech / CRO
- Hands-on experience conducting and overseeing GCP Quality Audits
- Experience in vendor / CRO oversight
- Degree in life-sciences (or equivalent)
What We Offer:
- Competitive salary, performance bonuses, stock options and a comprehensive benefit package
- A collaborative, growth-focused environment within a successful, global biotech
Get in Touch:
For more information, contact Guled Samatar at Meet:
- Call: 646-582-3675
- Email: guled.samatar@meetlifesciences.com
