Program Manager Jobs

10,000 jobs found — updated daily

About The Position

The Associate Director, Clinical Supply Project Manager (Program CSPM) works in Global Clinical Supply (GCS) Planning, which manages the end-to-end integrated clinical supply chain across the Research & Development portfolio. Planning serves as a key interface between clinical development teams and the operational organizations responsible for clinical supply execution. The Program CSPM is the program-level GCS Planning point of contact for internal and external customers and the lead GCS spokesperson at clinical and development-related meetings. Working independently, the position designs strategic and operational plans for clinical supply activities across assigned compounds or programs. It coordinates with clinical development, regulatory, quality, and supply chain partners; establishes bulk manufacturing and drug-product release timelines; manages forecasts and bulk supply allocation; and identifies and escalates significant supply risks. The role is accountable for program clinical supply budgets and supports protocol and program cost estimates, documentation for labeling, packaging, and critical CMC activities, and collection of supply-chain metrics. The position also contributes subject-matter expertise to non-pipeline activities, mentors team members, supports staff development, and drives continuous improvement in clinical supply planning processes and systems. It contributes to departmental strategy and cross-functional projects, while applying sound judgment to unstructured problems and balancing strategic planning with tactical execution. The role emphasizes customer and patient focus, disciplined decision-making, ethics, and integrity.

Requirements

  • Bachelor’s degree in a scientific, business, or related discipline.
  • At least 8 years of experience in project management, clinical supply planning, scheduling, coordination and processing of supply-chain activities, pharmaceutical development, clinical operations, or related biopharmaceutical functions.
  • Excellent communication and interpersonal skills, including the ability to communicate effectively with cross-functional teams, senior management, external vendors, and clinical sites.
  • Strong negotiation, influencing, and relationship-building skills to support alignment and collaboration in supply planning.
  • Strong knowledge of project management principles and clinical customer relationship management.
  • Familiarity with supply-chain systems and software such as SAP or Oracle, demand-planning principles, and Microsoft Excel, PowerPoint, and Word.
  • Strong analytical and problem-solving skills, including the ability to analyze complex data, identify trends, and make data-driven decisions to optimize supply-chain processes.
  • Ability to thrive in a fast-paced, dynamic environment and adapt quickly to changing business needs and priorities.
  • Strong attention to detail and organizational skills, including the ability to manage complex supply-chain activities, multitask, prioritize, and meet tight deadlines.
  • Proactive approach to identifying process inefficiencies, developing solutions, and driving continuous improvement.
  • Proven record in project or portfolio management.

Nice To Haves

  • Master’s degree or MBA preferred.
  • Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP) is highly desirable.
  • Proficiency with supply-chain management systems and software, including ERP systems such as SAP, demand-planning tools, and inventory-management systems.
  • Familiarity with data analytics and visualization software.
  • Familiarity with GMP requirements, quality procedures, and Standard Operating Procedure (SOP) execution.

Responsibilities

  • Represent GCS Planning as the lead program representative and primary GCS point of contact for internal and external customers; serve as the lead GCS spokesperson at clinical and development-related meetings.
  • Design strategic and operational plans for clinical supply activities across assigned compounds and programs.
  • Coordinate with clinical development, regulatory, quality, and supply-chain partner organizations to negotiate timelines, strategies, and other clinical supply topics.
  • Establish timelines for bulk manufacturing needs and drug-product release across assigned programs.
  • Use SAP to establish a consolidated, visible forecast for products used within assigned programs, including bulk drug product.
  • Oversee bulk drug supply management and ensure appropriate allocation across studies within assigned programs.
  • Identify significant risks in clinical bulk supply activities and lead escalation and subsequent management of clinical supply issues with GCS Leadership.
  • Manage the clinical supply budget for assigned programs and support protocol and program cost estimates requested by Product Development Teams.
  • Author clinical supply documentation supporting labeling and packaging activities, as well as supply-chain documentation supporting critical CMC activities.
  • Support collection of clinical supply-chain metrics and participate in critical non-pipeline activities as a subject-matter expert.
  • Mentor new team members and support staff development as needed.
  • Solve unstructured problems, make informed decisions considering technical and business risks, and influence portfolio decisions using facts and data.
  • Balance strategy with tactical execution and maintain ownership and accountability for assigned work.
  • Drive continuous improvement to enhance the efficiency, accuracy, and effectiveness of clinical supply planning processes and systems.
  • Stay current on industry trends, regulations, and best practices related to clinical supply planning and incorporate them into team operations.
  • Contribute to departmental strategy and participate in cross-functional projects to advance continuous improvement and efficiency efforts.
  • Focus on customers and patients, make rapid and disciplined decisions, and demonstrate ethics and integrity.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Other insurance benefits for employees and family
  • Retirement benefits, including 401(k)
  • Paid holidays
  • Vacation
  • Compassionate days
  • Sick days
  • Annual bonus eligibility
  • Long-term incentive eligibility, if applicable

Career Resources

Build a Resume for Program Manager

The resume builder that gets results.

  • Get clear feedback so you look as qualified as you are
  • Align your resume with the job to get further in the process, faster
  • Take the guesswork out of resume writing

Explore Related Job Searches

© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service