Senior Manager/Associate Director, Clinical GCP Quality

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 that includes a suite of gene editing and delivery technologies and is in the process of building 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 potential 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

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Position Overvie

w:
Beam is seeking a highly talented and motivated Senior Manager / Associate Director – Clinical GCP Quality to join our growing Quality team. The Senior Manager / Associate Director – Clinical GCP Quality will be responsible for quality aspects of Beam’s clinical studies and overall Good Clinical Practice (GCP) as the company grows and continues to evolve from a research and discovery (R&D) company to a broader organization moving products though the clinical pipeline to commercial launch and growth. Reporting to the Senior Director – Clinical GCP Quality, this position will be a key member of Beam’s Quality organization, as well as clinical study team(s) working with Clinical Development functional-area leads to ensure appropriate levels of clinical compliance and quality. Additionally, this position may assist Non-clinical Development (NCD) and Clinical Bioanalytics & Translational Sciences (CBTS) colleagues with qualification activities of third-party laboratori

es.
Responsibilit

• ies:
  Assist the Senior Director – Clinical GCP Quality in helping to define and drive the clinical compliance and quality vision and mindset within the com
• pany.Continue to improve/refine Beam’s risk based GCP compliance program as the company moves from developmental to commercial (i.e., R&D, clinical research pipeline, commercial launch, gro
• wth).Ensure appropriate quality systems are in place to qualify clinical and non-clinical suppliers, which may include laboratories conducting regulated activities (clinical and non-clinical), clinical sites, and clinical study-related documents as they relate to GCP compli
• ance.Oversee clinical compliance and quality within the context of a clinical study tea
• m(s).Oversee quality aspects related to clinical study start-up, execution, and close-out by providing leadership, guidance, and direction to staff consistent with
• GCP.Ensure appropriate escalation of significant issues that may impact patient safety, the reliability of clinical study results, product quality and/or supply, regulatory compliance, and/or company brand i
• mage.Partner with Sr. Director on strategy for managing multiple suppliers including full service
• CROs.May assist NCD and CBTS with qualification/requalification activities (questionnaires, audits, quality technical agreements, e
• tc.).May provide GxP auditing activities, including audit preparation, execution, report preparation, and follow-up to any findings/observations, including corrective and preventive actions (CA
• PAs).May assist in preparation for health authority inspections at Beam, suppliers, and/or clinical s

ites.
Qualifica

• tions:
  University degree in scientific discipline/life sciences OR equivalent experience in biotech or pharmaceutical i
• ndustry10 years of relevant experience in quality, 5 in a GCP environment with at least three years of demonstrated experience working with multi-disciplinary functional areas. Level will be commensurate with expe
• rience.Knowledge and experience in a GLP environment is pre
• ferred.Solid knowledge of global regulatory requirements/standards for the pharmaceutical, biotech, or vaccine industry (experience in cell and/or gene therapies, a
• plus).Positive ap
• proach.Excellent interpersonal effectiveness and written/verbal listening/communication
• skills.Excellent computer skills (quality and document management systems, clinical study-related systems (e.g., electronic data capture, interactive response technology, clinical trial management, etc.), and Microsoft products and services (e.g., Excel, PowerPoint, Visio, Word,
• etc.).Highly attentive to details and able to work well as part of
• a team.Demonstrates consistent quality, judgment, accuracy, speed, and crea
• tivity.Takes initiative in making improvement suggestions to promote operational
• goals.Applies quality concepts and company policies/standards to resolve issues of moderate complexity in an effective
• manner.Facilitates designing processes with quality built in from the beg
• inning.Identifies and uses good judgment to handle out-of-compliance sce
• narios.Ability to work indepen