Planet Pharma
Overview
Responsible for managing drug supply planning, inventory control, and distribution activities related to clinical supplies on multiple clinical programs. Works closely with CMC, Regulatory Affairs, Quality Assurance, Clinical Operations, and external partners/CMOs as needed to build strong relationships, support study project teams, and ensure timely Investigational Product (IP) for clinical trials.
Responsibilities Lead and manage end-to-end Clinical Supply Chain activities (planning, packaging and labeling, distribution, returns and destruction) for assigned clinical programs in early and late phases.
Develop and manage supply forecasts, supply plans, and timelines in collaboration with Clinical and CMC.
Manage IP inventory levels at depots and clinical sites; coordinate inventory from manufacturer to depot or clinical sites.
Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
Ensure effective management of IP based on study timing and in accordance with clinical protocols, cGMP, GCP, ICH, FDA, and other applicable regulations.
Collaborate with Clinical Operations, CMC, Regulatory Affairs, QA, and PDM to advance clinical programs and ensure supplies readiness.
Manage clinical supply and logistics and resolve issues such as shipment delays and temperature excursions; coordinate with internal Trade Compliance & Logistics team.
Demonstrate understanding of clinical study design (randomized, blinded, open label, etc.) and execution.
Manage clinical trial contracts and purchase orders including invoices and budgets for clinical supply vendors; participate in CSC budget and forecast planning.
Represent the Clinical Supply Chain function at clinical trial meetings and communicate plans and timelines to internal and external customers and partners.
Qualifications Education: BS/BA degree (Masters preferred) in life sciences or business or equivalent required.
Experience: Minimum 5–7 years in life sciences industry including Project Management, Pharmaceutical Development, Clinical Supply Management, and/or Clinical Trials Coordination; at least 3+ years in Clinical Supplies Management.
Skills: Proficient knowledge of Microsoft Excel, PowerPoint, and Project software.
Certifications: APICS certification (CPIM, CLTD, CSCP) preferred.
Note
Pay ranges between $85-103/hr based on experience. The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Details Job function: Management and Manufacturing
Employment type: Full-time
Seniority level: Not Applicable
Other job postings and salary ranges listed in the original description have been omitted to maintain a concise, focused posting.
#J-18808-Ljbffr
Responsible for managing drug supply planning, inventory control, and distribution activities related to clinical supplies on multiple clinical programs. Works closely with CMC, Regulatory Affairs, Quality Assurance, Clinical Operations, and external partners/CMOs as needed to build strong relationships, support study project teams, and ensure timely Investigational Product (IP) for clinical trials.
Responsibilities Lead and manage end-to-end Clinical Supply Chain activities (planning, packaging and labeling, distribution, returns and destruction) for assigned clinical programs in early and late phases.
Develop and manage supply forecasts, supply plans, and timelines in collaboration with Clinical and CMC.
Manage IP inventory levels at depots and clinical sites; coordinate inventory from manufacturer to depot or clinical sites.
Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
Ensure effective management of IP based on study timing and in accordance with clinical protocols, cGMP, GCP, ICH, FDA, and other applicable regulations.
Collaborate with Clinical Operations, CMC, Regulatory Affairs, QA, and PDM to advance clinical programs and ensure supplies readiness.
Manage clinical supply and logistics and resolve issues such as shipment delays and temperature excursions; coordinate with internal Trade Compliance & Logistics team.
Demonstrate understanding of clinical study design (randomized, blinded, open label, etc.) and execution.
Manage clinical trial contracts and purchase orders including invoices and budgets for clinical supply vendors; participate in CSC budget and forecast planning.
Represent the Clinical Supply Chain function at clinical trial meetings and communicate plans and timelines to internal and external customers and partners.
Qualifications Education: BS/BA degree (Masters preferred) in life sciences or business or equivalent required.
Experience: Minimum 5–7 years in life sciences industry including Project Management, Pharmaceutical Development, Clinical Supply Management, and/or Clinical Trials Coordination; at least 3+ years in Clinical Supplies Management.
Skills: Proficient knowledge of Microsoft Excel, PowerPoint, and Project software.
Certifications: APICS certification (CPIM, CLTD, CSCP) preferred.
Note
Pay ranges between $85-103/hr based on experience. The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Job Details Job function: Management and Manufacturing
Employment type: Full-time
Seniority level: Not Applicable
Other job postings and salary ranges listed in the original description have been omitted to maintain a concise, focused posting.
#J-18808-Ljbffr