Senior Manager / Associate Director, Clinical Quality Assurance
Required skills
- Clinical Quality Assurance
- GCP
- GCLP
- GVP
- CROs
- vendor oversight
- audits
- CAPA
- inspection readiness
- ICH E6 R3
Nice to have
- ASQ CQA
- RQAP-GCP
- Veeva
Role summary
The Senior Manager / Associate Director of Clinical Quality Assurance (CQA) will lead the qualification and ongoing quality oversight of CROs and other clinical service providers, offering clinical quality support for assigned studies. This role involves implementing risk-based vendor oversight, managing vendor quality and compliance risks, and providing GCP guidance to study teams. Responsibilities include supporting quality investigations, audits, CAPAs, and inspection readiness to ensure effective sponsor oversight and clinical trial compliance. The position requires a university degree in a scientific discipline and 7+ years of relevant experience in clinical/GCP quality, with at least 3 years in conducting or managing GCP vendor and investigator site audits.
Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
The Senior Manager / Associate Director of Clinical Quality Assurance (CQA) will provide leadership for the qualification and ongoing quality oversight of CROs and other clinical service providers while providing clinical quality support for assigned studies. This role will partner cross-functionally to implement risk-based vendor oversight, monitor and address vendor quality and compliance risks, and provide pragmatic GCP guidance to study teams. This position will also support quality investigations, audits, CAPAs, and inspection readiness activities to ensure effective sponsor oversight and sustained clinical trial compliance.
Responsibilities:
Qualifications:
The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Beam Pay Range$155,000—$225,000 USDSimilar roles
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