University degree in a scientific discipline/life sciences.
7+ years of relevant experience in clinical/GCP quality.
3+ years of experience conducting or managing GCP vendor and investigator site audits.
Professional audit certification (e.g., ASQ CQA, RQAP-GCP) preferred.
Strong knowledge of GCP and applicable FDA, EMA, MHRA and ICH requirements.
Responsibilities
Lead and manage the qualification and ongoing quality oversight of CROs and other GCP/GCLP/GVP service providers.
Maintain a risk-based vendor qualification and oversight framework, including audits and documentation of vendor quality status.
Partner with study team members to ensure appropriate quality oversight of associated vendors.
Determine overall audit strategy/schedule for external vendors, including internal vs outsourced audits.
Support QA leadership for significant vendor quality issues, including investigations and CAPA development.
Execute program/study-level risk-based audit plans, including site and vendor audits.
Support enterprise-wide GCP inspection readiness strategies and plans.
Benefits
Opportunity to work in a dynamic clinical stage biotech environment.
Collaborative cross-functional team culture.
Focus on professional development and continuous learning.
Engagement in innovative quality management practices.
Full Job Description
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:
Lead and manage the qualification and ongoing quality oversight of CROs and other GCP/GCLP/GVP service providers supporting clinical development.
Maintain a risk-based vendor qualification and oversight framework, including qualification assessments, audits, periodic re-assessments and documentation of vendor quality status.
Partner with study team members to ensure appropriate quality oversight of associated vendors.
Determine overall audit strategy / schedule for external GCP/GCLP/GVP vendors, including which audits to conduct internally vs outsource.
Support QA leadership for significant vendor quality issues, including investigations, RCA, CAPA development/assessment, and effectiveness.
Support the development of and execute program/study-level risk-based audit plan, including investigator site, vendor and internal process audits.
Support execution of enterprise-wide GCP inspection readiness strategies and plans.
Partner cross-functionally to promote effective sponsor oversight of outsourced activities consistent with ICH E6 R3 expectations.
Serve as the Clinical QA Support for assigned studies and programs.
Provide quality review of protocols, informed consent forms, investigator brochures, CSRs, and regulatory submission documents as requested.
Contribute to the continued evolution of the Quality Management System, including oversight and trending of key quality metrics (internal and external).
Support clinical and QA SOP development efforts.
Ensure adherence to GxP requirements and SOPs.
Embody Beam's cultural values and align daily actions with departmental goals and company culture.
Qualifications:
University degree in a scientific discipline/life sciences.
Experience in a clinical stage biotech company preferred.
7+ years of relevant experience in clinical/GCP quality. Level will be commensurate with experience.
3+ years of experience conducting or managing GCP vendor and investigator site audits.
Professional audit certification (e.g., ASQ CQA, RQAP-GCP) preferred.
Direct experience qualifying and overseeing CROs and other service providers.
Strong knowledge of GCP and applicable FDA, EMA, MHRA and ICH requirements.
Demonstration ability to successfully partner cross-functionally.
Excellent interpersonal effectiveness, including exceptional communication skills.
Advanced computer skills, including experience working in Veeva.
Consistent excellent judgement and pragmatic, risk-based decision making skills.
Strong team player that has a customer service approach and is solution oriented.
Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
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 USD
About Beam Therapeutics
Beam Therapeutics is a biotechnology company focused on developing precision genetic medicines using its proprietary base editing technology. The company's platform allows for precise and efficient editing of single base pairs in DNA and RNA, which has the potential to treat a wide range of genetic diseases. Beam Therapeutics' lead product candidate, BEAM-101, is a potential treatment for sickle cell disease and beta-thalassemia. The company was founded in 2017 and is headquartered in Cambridge, Massachusetts.
