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Project Manager - Clinical Packaging
Job in
Newark, Essex County, New Jersey, 07175, USA
Listed on 2026-02-12
Listing for:
Verbatim Pharma
Full Time
position Listed on 2026-02-12
Job specializations:
-
Manufacturing / Production
Packaging Engineer
Job Description & How to Apply Below
Position Overview: We are seeking a highly motivated Clinical Project Manager with extensive experience in clinical packaging and supply chain management to join our team.
The ideal candidate will have a minimum of four years of experience in the clinical packaging industry, including at least one year of proven success as a Project Manager. This position will be instrumental in managing the successful execution of clinical trial packaging projects, from initiation to completion, ensuring all project requirements, timelines, and quality standards are met.
Key Responsibilities:
- Client & Internal Liaison:
Act as the main point of contact for clients, coordinating with internal departments to ensure project requirements are met throughout the clinical trial lifecycle. - Project Management:
Lead clinical packaging projects from initiation through completion, managing timelines, deliverables, and change orders. - Packaging Design & Execution:
Develop and oversee packaging specifications, including kit layout, labelling, and component selection, aligned with study protocols. - Documentation & Compliance:
Ensure accurate preparation and approval of packaging documentation, labels, and regulatory materials, in compliance with GMP/GDP standards. - Material Sourcing & Inventory Control:
Manage sourcing of packaging materials, monitor inventory levels, and coordinate product destruction at the end of the study. - Stakeholder Communication & Audits:
Facilitate regular client updates, meetings, and audits, ensuring clear communication and adherence to quality standards.
Qualifications:
- Bachelor’s degree in a related field or equivalent work experience.
- A minimum of 4 years of experience in the clinical packaging environment, with at least 1 year in a project management role.
- In-depth knowledge of clinical trial materials and packaging requirements, including GMP and GDP.
- Strong communication, organizational, and interpersonal skills.
- Attention to detail with a high level of accuracy in all aspects of the job.
- Ability to manage multiple projects simultaneously and meet tight deadlines.
- Proficient in project management software and Microsoft Office Suite.
- Strong problem-solving abilities and the capacity to navigate complex project requirements.
If this role sounds of interest, please contact Amelia at Verbatim Pharma by emailing or submit your application today!
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