Program Manager – Clinical Trials & Drug Product Manufacturing

Location: Only candidate located in Mexico

Remote

Position Summary

We are seeking an experienced Program Manager to lead and coordinate strategic initiatives focused on Clinical Trials and Drug Product Manufacturing within the pharmaceutical/life sciences industry. This individual will be responsible for managing cross-functional programs, driving execution, mitigating risks, and ensuring projects are delivered on time, within scope, and aligned with business objectives.

This is a remote position , and candidates must be based in Mexico .

Key Responsibilities

- Lead end-to-end program management for clinical development and drug product manufacturing initiatives.
- Coordinate cross-functional teams including Clinical Operations, Manufacturing, Quality, Regulatory Affairs, Supply Chain, CMC, and external partners.
- Develop and maintain integrated project plans, timelines, milestones, budgets, and risk management plans.
- Monitor program progress and proactively identify, communicate, and resolve risks, issues, and dependencies.
- Facilitate governance meetings, executive status updates, and stakeholder communications.
- Ensure alignment between clinical trial activities and manufacturing readiness.
- Collaborate with internal teams and external vendors/CMOs to ensure successful program execution.
- Drive continuous improvement in project management processes and best practices.
- Support strategic planning and decision-making through accurate reporting and data-driven insights.





Required Qualifications

- Bachelor's degree in Life Sciences, Pharmacy, Chemistry, Engineering, or a related discipline.
- Minimum 8 years of Program or Project Management experience , preferably leading complex cross-functional programs.
- Proven experience in Clinical Trials and Drug Product Manufacturing .
- Experience within the Life Sciences, Biotechnology, or Pharmaceutical industry .
- Strong understanding of the drug development lifecycle, including clinical development and manufacturing processes.
- Excellent stakeholder management and cross-functional leadership skills.
- Outstanding verbal and written communication skills.
- Strong organizational, planning, and problem-solving abilities.
- Ability to manage multiple priorities in a fast-paced, general environment.

Preferred Qualifications

- PMP, PgMP, or equivalent Project Management certification.
- Experience working with Contract Manufacturing Organizations (CMOs/CDMOs).
- Familiarity with GxP, GMP, ICH guidelines, and regulatory requirements.
- Experience managing global or international programs.
- Knowledge of Agile and traditional project management methodologies.

Required Skills

- Program Management
- Clinical Trials
- Drug Product Manufacturing
- Pharmaceutical Industry
- Life Sciences
- Cross-functional Leadership
- Risk Management
- Stakeholder Management
- Executive Communication
- Project Planning
- Budget & Timeline Management
- Vendor Management

Location

- Remote
- Candidates must reside in Mexico.

📌 Program Manager – Clinical Trials & Drug Product Manufacturing (México)
🏢 Luttechub
📍 México