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Director Biorepository Jobs (NOW HIRING)

Exact Sciences

Director, Clinical Pathology

Phoenix, AZ · On-site

$79.40K - $108.20K/yr

Position Overview The Director, Clinical Pathology serves as a surgical pathology expert in the ... Biorepository, Quality Assurance, Quality Control, Service Engineering, Process Engineering ...

Vanderbilt Health

Manager, Laboratory

Nashville, TN

Direct day-to-day biorepository and laboratory operations supporting academic and commercial investigators. * Optimize workflows related to tissue procurement, processing, annotation, storage, and ...

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Director Biorepository information

What are the key skills and qualifications needed to thrive as a Director Biorepository, and why are they important?

To thrive as a Director Biorepository, you need expertise in biospecimen management, regulatory compliance, and a background in life sciences, often supported by an advanced degree such as a PhD or MSc. Familiarity with laboratory information management systems (LIMS), biobanking software, and quality assurance certifications like ISO 20387 is typically required. Strong leadership, organizational skills, and effective communication help manage teams and collaborate with researchers and stakeholders. These skills ensure the integrity, traceability, and ethical handling of biospecimens, which are crucial for supporting high-quality research and clinical outcomes.

What are the primary challenges a Director Biorepository faces in maintaining compliance with regulatory standards?

As a Director Biorepository, one of the main challenges is ensuring that all biospecimen collection, storage, and distribution practices align with evolving regulatory standards such as HIPAA, GDPR, and Good Laboratory Practice (GLP). This involves regularly updating protocols, providing training to staff, and implementing robust quality management systems. Additionally, directors must coordinate audits, manage documentation, and quickly address any non-compliance findings to maintain accreditation and partner trust.

What are Director Biorepository responsibilities?

A Director of Biorepository oversees the management and operation of biorepositories, which are facilities that store biological samples for research and clinical purposes. Their responsibilities include ensuring proper sample collection, storage, and tracking, maintaining quality control standards, and overseeing staff. They also develop and implement policies for biospecimen handling, ensure compliance with regulatory requirements, and coordinate with researchers and stakeholders to support scientific studies.

What is the difference between Director Biorepository vs Laboratory Manager?

AspectDirector BiorepositoryLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., PhD, MS) and industry-specific certificationsUsually requires a bachelor's or master's degree in a related field
Work EnvironmentOversees biorepository facilities, managing sample storage, cataloging, and complianceManages daily laboratory operations, staff, and testing procedures
Industry UsageCommonly found in biotech, pharmaceutical, and research institutionsFound across various research labs, hospitals, and clinical settings

The Director Biorepository focuses on strategic oversight of sample storage and biobanking, requiring specialized credentials and industry experience. In contrast, the Laboratory Manager handles operational management of laboratory activities, often with a broader scope of laboratory functions. Both roles are essential in research and healthcare environments but differ in scope and responsibilities.

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Director Biorepository jobs near you
Director, Translational Operations

Director, Translational Operations

Allogene Therapeutics

South San Francisco, CA • On-site, Remote

$200K - $230K/yr

Full-time

Medical

Posted 4 days ago

Job description

Job Description
About Allogene:
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
About the role:
Allogene is seeking a Director, Translational Operations to provide strategic and hands-on leadership for biospecimen operations across Allogene clinical programs. This individual will oversee internal FTEs and external vendors responsible for biospecimen collection, kitting, shipping, receipt, accessioning, storage, chain-of-custody, and sample analysis (e.g., central labs, specialty assay vendors, biorepositories, couriers, and kit providers). The ideal candidate thrives in a fast-paced and dynamic environment, can roll up their sleeves, and brings deep expertise in operationalizing translational sample workflows to enable high-quality, analyzable clinical and biomarker data.
The Director, Translational Operations will report to the Vice President of Research and Translational Science and will partner closely with Translational Sciences, Clinical Operations, Clinical Development, Biometrics/Data Management, Quality, Regulatory, and external collaborators to ensure robust, scalable, and inspection-ready sample operations that enable high-quality biomarker and translational readouts. This is a hybrid role based at our headquarters in South San Francisco, CA (US based remote may be considered as well for candidates outside of the area).
Responsibilities include, but are not limited to:
  • Own the end-to-end biospecimen operational strategy for clinical studies, ensuring feasibility, scalability, quality, and timeline alignment from protocol design through database lock and long-term storage.
  • Lead internal teams and external vendors dedicated to biospecimen workflows, including vendor selection, qualification, oversight, performance management, and issue escalation.
  • Partner cross-functionally to integrate biospecimen requirements into protocols, lab manuals, informed consent language, and operational plans.
  • Develop and maintain sample lifecycle process maps (collection, shipment, receipt, processing, storage, analysis, data transfer), including clear roles and responsibilities across Allogene and vendors.
  • Oversee kit design and distribution, site training materials, and operational guidance to enable consistent, high-quality collections across domestic and ex-US sites.
  • Establish and monitor KPIs/KQIs for biospecimen operations (e.g., collection compliance, shipment timeliness, temperature excursions, sample integrity, query/issue rates, assay turnaround time, vendor data delivery).
  • Own chain-of-custody, labeling standards, reconciliation, deviations, and CAPA processes for biospecimens, including systematic root-cause analysis and prevention.
  • Ensure inspection-ready operations consistent with applicable GxP/GCLP principles, internal procedures, and vendor quality agreements; support audits and inspections as needed.
  • Drive vendor governance (standing meetings, performance reviews, risk registers, forecast alignment, and change control), ensuring vendors deliver to SOW, quality expectations, and timelines.
  • Own and maintain budgets and forecasts for translational/biospecimen operations; partner with Finance/Procurement on contracting and invoice/PO processes as applicable.
  • Enable robust data flow and traceability by coordinating vendor deliverables (e.g., manifests, accessioning logs, LIMS exports, assay result files) and ensuring timely, high-quality transfer to Allogene systems/partners.
  • Provide cross-functional operational support to enable efficient execution of Translational Science activities across multiple programs
  • Mentor and develop team members supporting translational operations; provide guidance to assess and resolve operational project issues; contribute to staffing plans and capability building.
  • Perform other duties as assigned.

Position Requirements & Experience
  • Bachelor's degree required in life sciences, bioengineering, clinical research, or a related field; advanced degree preferred with at least 10 years of relevant industry experience in translational operations, clinical sample operations, central lab operations, clinical laboratory services, or biomarker operations, with at least 5 years in a leadership role.
  • Demonstrated expertise building and running biospecimen operational workflows across multi-site clinical trials, including collection logistics, cold-chain shipping, biorepository operations, and specialty assay vendor oversight.
  • Strong working knowledge of clinical research operations and expectations for sample handling integrity, traceability, and documentation; experience supporting early to late-stage trials preferred.
  • Proven ability to select, manage, and hold vendors accountable through SOWs, KPIs, governance, and continuous improvement.
  • Excellent organizational skills and an ability to prioritize effectively to deliver results within established timelines and budgets.
  • Strong interpersonal, written, and verbal communication skills; able to collaborate effectively across functions and with senior stakeholders.
  • Comfortable in a fast-paced environment with evolving priorities; pragmatic problem solver with high ownership and follow-through.
  • Willingness and ability to travel domestically and internationally as required.
  • Candidates must be authorized to work in the U.S.

Preferred Qualifications
  • Experience in cell therapy and/or oncology clinical trials, including complex sample handling and time-sensitive logistics.
  • Experience with global sample operations (ex-US shipping, import/export documentation, courier qualification, regional lab networks).
  • Familiarity with LIMS/data interfaces and operationalizing biomarker data transfers into clinical databases or analytics environments.
  • Experience partnering with Quality on vendor audits, quality agreements, QMS expectations, and inspection readiness.

We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected salary range for this role is $200,000 - $230,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought, designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.
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