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Director/Senior Director, Apheresis Operations
Beam Therapeutics Cambridge, MA
$136k-172k (estimate)
Full Time | Durable Manufacturing 1 Month Ago
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Beam Therapeutics is Hiring a Director/Senior Director, Apheresis Operations Near Cambridge, MA

Company Overview

Beam Therapeutics is 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.

Position Overview:

Beam is seeking a highly talented and motivated (Senior) Director, Apheresis Operations for ex vivo therapeutics. This role will create and build a new Apheresis Operations function within Patient Supply. This will foster close communication with cross function Beam Team members such as Medical, Clinical Operations, Product Development, Manufacturing, and Quality Assurance. 

Responsibilities:

  • Build new Apheresis Operations function that is focused on delivering excellent patient and stakeholder experience for clinical trials as it relates to the collection of patient cells.
  • Partner with clinical, quality, patient supply teams to build a robust collection network to support internal portfolios including:
    • Site selection, technical assessments training and onsite support.
    • Communicate and implement changes which affect apheresis site operations while aligning with regulatory authorities as required.
  • Serve as a key member of the clinical development team and optimize study documents (eg. protocol and cell handling manuals) to increase cell collection.
  • Provide apheresis expertise to support various internal activities such as regulatory submissions, protocol development and other quality processes.
  • Create and conduct Apheresis and Cell therapy lab on-boarding, assessments, training, and collection support and other areas as needed. Assist in the implementation of ISBT-128 ST-018, as needed.
  • Build metrics program that will drive data collection and analysis in support of optimizing collection procedures, efficiency, and quality.
  • Actively engage in the identification, sharing, and adaptation of best practices cross-functionally and between clinical trial sites.
  • Work closely with the Patient Supply, Supply Chain, Manufacturing, Quality, and Clinical functions to ensure the Chain of Identity of patient cell collection through the patient treatment pathway.
  • Identify and champion industry working group initiatives that will improve the overall Cell and Gene Therapy Industry and the treatment experience of our patients.
  • Coach, develop and mentor a high-performing team with a vision of setting industry-leading standards.

Qualifications

  • Bachelor's degree or the combination off education and business experience required.
    • Advanced degree preferred (e.g., MBA, RN, MPH, etc.)
    • Minimum 10 years (15 years) of healthcare or related experience, including significant experience within the biotech industry (especially with cell and gene therapy products).
  • Strong preference for experience within Sickle Cell Disease and autologous cell & gene therapy.
  • Strong direct apheresis experience within the last 5 years.
  • Qualification in Apheresis (QIA) certification preferred
  • Ability to work independently with very limited supervision
  • Ability to navigate and be successful in a fast-paced, highly matrixed work environment.
  • Detail-oriented, able to assess and assimilate data and communicate objectively
  • Experience in conducting clinical trials and working with clinical research teams
  • Good knowledge of GCPs, GMPs, AABB, FACT/JACIE, FDA, EMEA, MHRA, regulations
  • Effective teaching, training, planning, and problem-solving abilities
  • Willingness to travel domestically (~10-25% of time)
  • Strong team player that has patient focused approach and is solution oriented.
  • Excellent listening, communication and interpersonal skills foster team spirit.
  • Excellent people management skills with multicultural background and a strong track record of developing people/talent and organizational capability.
  • A passion for addressing the critical unmet medical needs of patients.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Durable Manufacturing

SALARY

$136k-172k (estimate)

POST DATE

03/09/2024

EXPIRATION DATE

05/08/2024

WEBSITE

beamtx.com

HEADQUARTERS

CAMBRIDGE, MA

SIZE

200 - 500

FOUNDED

2017

CEO

JOHN EVANS

REVENUE

<$5M

INDUSTRY

Durable Manufacturing

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