Vaxcyte

Senior Manager, Clinical Supply

Vaxcyte$158K — $185K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Supply Chain, or Logistics; advanced degrees are a plus.
  • 9+ years' experience in Clinical Supply Management.
  • Experience with Blinded personnel and clinical supplies.
  • Prior involvement in vaccine trials is highly desired.
  • Familiarity with Veeva Vault is a strong plus.
  • Knowledge of global regulatory labelling requirements for clinical trials.
  • Experience in Cold Chain packaging and logistics.

Responsibilities

  • Determine vaccine and comparator demand based on trial specifics.
  • Translate demand plans into actionable supply plans.
  • Collaborate with stakeholders to develop detailed packaging run projects.
  • Conduct scenario planning for protocol designs and supply risks.
  • Manage execution of packaging plans and address any issues.
  • Oversee Clinically Labelled Drug Product label text development and approvals.
  • Monitor trial execution and adjust supply plans to ensure continuity.

Benefits

  • Comprehensive benefits package.
  • Equity component included.
  • Hybrid work arrangement with minimum 2-3 days onsite.
Full Job Description
Summary:

Vaxcyte is seeking a Sr. Manager, Clinical Supply, to lead clinical demand and supply planning, along with the planning and execution of clinical packaging runs. This role will be instrumental to ensure that our trials have sufficient vaccine and comparator supply to start as planned and continue to completion without any interruptions.
Essential Functions:
  • Determine vaccine & comparator demand based on protocol, # of sites, shelf life, & risk.
  • Translate demand plan into a supply plan (#, timing volume of packaging runs).
  • Work closely with clinical secondary packaging sites, central and sub-depots and key stakeholders in Clinical Operations, Regulatory, Quality, Supply Chain, & Process Development to develop detailed project plan for each packaging run.
  • Scenario planning based on potential different protocol designs or supply chain risks.
  • Develop detailed project plan for each packaging run.
  • Manage execution of packaging plan, and resolve / escalate issues as needed.
  • Manage Clinically Labelled Drug Product label text/proof development, and Approval following regulatory guidelines, and in Veeva.
  • Batch records pre-, and post-production review, and approval in Veeva.
  • Collaborate with QA on central depot document management in Veeva.
  • Partner with Clinical on IRT selection, implementation, and UAT.
  • Manage cold-chain logistics for Clinically Labelled Drug Product.
  • Inventory management for depots, and clinical sites.
  • Monitor trial execution vs plan and drug shelf life and make adjustments to supply plan as needed to maintain supply continuity.
  • Maintain Clinical supply dashboard and metrics.
  • Maintain Batch Genealogy database.
  • Resolve temperature excursions in storage depots, during shipping, and at clinical sites.
  • Perform inventory reconciliation at end of trial.
  • Ensure excess packaged inventory at end of trial is disposed of in a compliant manner.
Requirements:

Bachelor's degree in Life Sciences, Supply Chain, or Logistics; advanced degrees are a plus. 9+ years' experience working in Clinical Supply Management. Other combinations of education and/or experience may be considered.
  • Experience working with Blinded personnel and clinical supplies.
  • Experience with vaccine trials highly desired.
  • Experience with Veeva Vault highly desired.
  • Experience with global regulatory labelling requirements for clinical trials.
  • Working knowledge of current GMP.
  • Experience with Cold Chain packaging, and logistics.
  • Experience with Reverse Distribution, Accountability, and Destruction.
  • Experience leading Cross-Functional teams.
  • Good verbal and written communication skills.

Reports to: Director, Clinical Supplies

Location: San Carlos, CA

Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy):

Hybrid (minimum of 2-3 days per week onsite)

Compensation:

The compensation package will be competitive and includes comprehensive benefits and an equity component.

Salary Range: $158,000 - $185,000 (SF Bay Area). Salary ranges for non-California locations may vary.

About Vaxcyte

Vaxcyte is a clinical-stage biotechnology company developing a new generation of vaccines to address some of the most important and deadly infectious diseases worldwide. The company's cell-free protein synthesis platform, comprising the XpressCFTM platform, is capable of rapidly generating protein antigens that can be used in vaccines to protect against bacterial and viral pathogens. Vaxcyte's lead vaccine candidate, VAX-24, is a preclinical, 24-valent pneumococcal conjugate vaccine (PCV) being developed for the prevention of pneumococcal disease. The company is also developing VAX-XP, a PCV with expanded serotype coverage, as well as vaccines for Group A Streptococcus, Group B Streptococcus, and Lyme disease.
Learn more about Vaxcyte
Size
89 employees
Market Cap
$3.6 billion
Industry
Founded
2013
NASDAQ

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