Senior Manager, Clinical Trial Supply & Logistics (Remote)

Parexel; Hartford (CT); Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Paid Time Off

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company Match

Pet Insurance

Job summary

Parexel is seeking a Manager, Production Services to lead the CTS&L team in a remote U.S./PA‑based capacity, with preference near Quakertown, PA. The role drives GMP‑compliant packaging, labeling, production planning, and batch documentation while partner­ing with global teams to ensure timely delivery of clinical trial materials.

You will shape the structure of a growing production services organization, provide operational leadership, and mentor a cross‑functional team to meet sponsor

Qualifications

• Bachelor’s degree and 6–10+ years in clinical trial supply chain or regulated pharma environment.
• Strong GMP knowledge and experience in packaging, labeling, and production planning.
• Proven project management, organizational, and stakeholder management skills.
• Fluent English communication.

Responsibilities

• Lead Production Services team and foster a high‑performance culture.
• Oversee clinical trial supply production workflows to stay on schedule.
• Monitor progress, manage priorities, and escalate complex supply chain issues.
• Support packaging, labeling, manufacturing support, and batch documentation.
• Ensure GMP, GDP, regulatory compliance and timely delivery.
• Collaborate with cross-functional stakeholders to ensure project success.

Skills

Leadership

Problem solving

Operational decision making

Communication skills

Cross-functional collaboration

Education

Bachelor’s degree in Life Sciences

Job description

Parexel is seeking a Manager, Production Services to lead the CTS&L team in a remote U.S./PA‑based capacity, with preference near Quakertown, PA. The role drives GMP‑compliant packaging, labeling, production planning, and batch documentation while partner­ing with global teams to ensure timely delivery of clinical trial materials.

You will shape the structure of a growing production services organization, provide operational leadership, and mentor a cross‑functional team to meet sponsor