TScan Therapeutics

Clinical Supply Chain Manager

TScan Therapeutics$130K — $140K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in operations, life sciences, or health-related field.
  • 8+ years in pharmaceutical/biotechnology industry focusing on clinical supply chain.
  • In-depth knowledge of GxP and FDA regulations related to clinical trials.
  • Strong communication skills for cross-functional collaboration.
  • Ability to diplomatically engage with senior management and vendors.
  • Skilled at prioritizing tasks in a dynamic environment.
  • Experience with electronic chain of custody systems (e.g., TrakCel).

Responsibilities

  • Develop and implement global clinical supply chain strategies for various clinical programs.
  • Collaborate with Clinical Operations to align drug delivery with dosing timelines.
  • Ensure accuracy of dosing information and approve shipping documentation.
  • Track shipments and resolve issues to meet delivery timelines and quality standards.
  • Monitor and manage drug product inventory levels while developing inventory trackers.
  • Support compliance by drafting and approving text for leukopaks and product labels.
  • Maintain audit-ready documentation and ensure all activities comply with GxP and FDA regulations.
  • Facilitate communication between internal teams and external stakeholders for clinical supply activities.
  • Manage the return and destruction process of drug products at trial sites.
  • Train clinical sites on clinical supply chain protocols.
  • Drive process improvements for efficiency and compliance in supply chain activities.

Benefits

  • Collaborative and vibrant company culture.
  • Opportunity to work in a fast-paced environment.
  • Exposure to oncology and cell therapy sectors.
  • Engagement with cross-functional teams and external vendors.
  • Eligibility for annual bonus and equity awards.
Full Job Description
Position Summary:

We are looking for a Sr. Manager, Clinical Supply Chain to oversee end-to-end supply chain activities to support our clinical studies. Reporting to the Sr. Director, Clinical Operations, the ideal candidate should have relevant experience in managing clinical supply chain activities for oncology or cell therapy products, and enjoy fast-paced, collaborative, and vibrant culture. A team player with a sense of urgency will thrive in this role.

Responsibilities:

  • Develop and execute global clinical supply chain strategies across multiple clinical programs.
  • Work closely with Clinical Operations to understand dosing timelines and place drug product orders to ensure timely delivery to clinical sites.
  • Ensure accuracy of drug product dosing information and approve final chain of custody and dosing documents.
  • Track shipments to clinical sites and triage issues during delivery ensuring adherence to timelines and quality standards.
  • Monitor drug product inventory levels and develop inventory trackers.
  • Support development and approval of text for leukopaks and drug product labels ensuring adherence to regulatory requirements.
  • Manage documentation related to temperature excursions during delivery and storage of drug product.
  • Maintain audit-ready documentation for all clinical supply chain activities and ensure compliance with GxP and relevant FDA regulations.
  • Develop and track budgets for all supply chain activities.
  • Facilitate communication and collaboration with internal teams (Clinical Operations, Regulatory, QC, QA, etc.) and external stakeholders (vendors, consultants) to ensure timely execution of clinical supply activities.
  • Manage interactions with clinical trial sites regarding the return and destruction of drug products.
  • Train clinical sites on clinical supply chain procedures.
  • Manage activities related to the electronic chain of custody system by managing the external vendor, managing updates to the system, conducting UAT, developing training material and training sites.
  • Drive process improvements and implement best practices to enhance efficiency, compliance, and scalability.


Requirements:

  • BS/BA or equivalent in operations, life sciences, or a health-related field.
  • Minimum of 8 years of experience in the pharmaceutical/biotechnology industry, with a focus on clinical supply chain, clinical trial material management, or related areas.
  • Strong understanding of GxP and FDA regulations governing clinical trials.
  • Excellent written and verbal communication skills, with the ability to collaborate effectively with cross-functional teams.
  • Strong interpersonal skills, with the ability to diplomatically interact with senior management, external vendors, and clinical trial sites.
  • Ability to prioritize tasks in a fast-paced, dynamic environment and manage multiple competing deadlines.
  • Familiarity with electronic chain of custody systems (e.g. TrakCel).


Pay Range: $130,000-$140,000

Pay Transparency

TScan Therapeutics' pay ranges are established based on external market data from third-party compensation surveys and our internal benchmarking. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Individual compensation within this range is commensurate with a candidate's specific qualifications, including education, overall experience, relevant experience, and specific skills. We strive to ensure that compensation is competitive, equitable, and aligned with the value each TScanner brings to the role.

Recruitment & Staffing Agencies

TScan Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics' internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of TScan Therapeutics, and TScan Therapeutics will not owe any referral or other fees with respect thereto.

About TScan Therapeutics

TScan Therapeutics is a biotechnology company that develops T-cell receptor therapies for the treatment of cancer. The company's platform uses a proprietary technology to identify and target cancer cells with high specificity. TScan's lead product candidate, TSC-100, is currently in Phase 1 clinical trials for the treatment of solid tumors. The company was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about TScan Therapeutics
Size
50 employees
Market Cap
$37.5 million
Industry
NASDAQ

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