Vice President, Compliance at Beam Therapeutics

Cambridge, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

28 Apr, 26

Salary

320000.0

Posted On

28 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Supplies Planning, Forecasting, Project Management, Regulatory Compliance, Cross-Functional Collaboration, Contract Management, Cold Chain Packaging, Labeling, Inventory Management, Clinical Trial Design, Quality Systems, Communication Skills, Problem Solving, GCP Training, Clinical Operations, Biopharmaceutical R&D

Industry

Biotechnology Research

Description

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 Vice President, Compliance is a strategic leader responsible for designing, implementing, and continuously improving the company’s Corporate Compliance Program to oversee promotional materials, field training, and HCP/patient programs. As an objective advisor, the Vice President, Compliance ensures the organization operates with integrity and in compliance with all applicable laws, regulations, and internal policies. Reporting to the Chief Legal Officer, the Vice President, Compliance partners with executive leadership, the legal and compliance function, the Audit Committee of the Board of Directors, and employees at all levels to foster a culture of ethical conduct and accountability. Beam is transitioning to a commercial stage company, and this position plays a critical role in developing a culture of compliance. Additionally, ex vivo cell therapy and in vivo gene therapy have unique commercial and operational needs that require a strategic leader to collaborate with commercial, medical, and manufacturing to build a commercial process that delivers for patients compliantly. Key Responsibilities: Responsible for Clinical Supplies Planning and Forecasting as required to meet program objectives, works with Clinical Operations and CMC to ensure timing of clinical trial investigational material needs are met. Work with cross function team Beam Team members (eg. Clinical Operations, QA and Regulatory) to create packaging strategies and label text for multiple countries/regions and provide support for regulatory filings as required. Provide technical expertise for the development of clinical study protocols and pharmacy manuals and will be required to develop dose preparation and administration strategies for complex gene editing products in early phases of development. Directly oversee and drive contract manufacturing packaging, labeling, national and international shipping/distribution operations for IMP (Investigational Medicinal Product) ensuring on time delivery to support clinical trials. Responsible for IRT requirements, user acceptance testing, and management. Outline clinical supply risks and propose mitigation plans. Independently execute the mitigation plans. Participate in business review meetings with third party drug supply vendors, as needed. Establish SOPs, protocols, and procedures for clinical trial material packaging, labeling and distribution to ensure compliance with cGxP requirements. Oversee vendor activities including procurement, labeling performance, on-time delivery, quality, improvement initiatives and issue resolution. Compile and report out execution operational metrics for the cross functional teams. Author pharmacy manual in conjunction with relevant cross functional leads. Develop drug supply training materials for investigational sites. Manage Quality Systems required documentation, including Deviations, Investigations, CAPA's, Change Controls, Label and Product Specifications, and others as required. Subject matter expert for clinical trial supply during regulatory inspections. Develop and apply Project Plans and Schedules that represent the appropriate level of detail and task independency. Ensure timely follow-up to all commitments in a project plan. Prepare supply and cost forecasts as required. Develop and manage clinical supply budget. Qualifications: BS in Pharmacy or related science. 10+ years of pharmaceutical experience with at least 7 years experience in clinical supplies managing complex projects. Prior investigational drug product experience and prior GCP training is required. Recent industry experience with clinical supplies or clinical operations is preferred. Demonstrated ability to work independently and with cross-functional teams, including Clinical Operations, CMC, Regulatory, Quality, and Finance. Demonstrated experience in managing third party contract clinical supply vendors. Demonstrated experience with global clinical supply forecasting, planning, packaging, labeling, inventory management, IVRS systems, and clinical trial designs for complex programs. Prior Cold Chain packaging, labeling, distribution experience required. IRT design and management experience required. Clinical Supplies Planning and Forecasting experience required. Prior Biopharmaceutical or pharmaceutical R&D experience preferred. Independent, self-driven, creative and capable problem-solver with solid communication skills. Experience in establishing and maintaining positive and collaborative relationships with key internal and external stakeholders. Working knowledge of ICH/GxP guidelines, FDA, MHRA, EMA, IRB/IEC and other applicable regulations/guidelines and demonstrated understanding of clinical research protocol requirements. Demonstrated proficiency with word processing, spreadsheet, database, presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint) Good organizational, communication and presentation skills, effective project and time management skills and the ability to work well under pressure. Desired: Advanced Degree in Pharmacy. Cell and Gene Therapy clinical supply experience. Direct Clinical Research Experience. 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 $210,000—$320,000 USD

Responsibilities

The Vice President, Compliance is responsible for designing and implementing the Corporate Compliance Program, overseeing promotional materials and HCP/patient programs. This role also involves collaborating with various teams to ensure compliance and ethical conduct within the organization.