Clinical Supply Chain Associate (HYBRID) - Innovative Company

Summary:

The Clinical Supply Chain Supply Associate supports programs and protocols, in tandem with program leads. This is a great opportunity to join a pharmaceutical company, and could also be a great transition for a CRC coming from a hospital setting.

Description:

• Interact with internal and external customers and suppliers in order to accomplish project objectives including packaging, labeling, shipment, inventory management, and drug return logistical activities.
• He/She manages and maintains IMP distribution and returns drug plans and manages Clinical Supply documentation associated with assigned program, in compliance with GMP and industry standards.
• The Supply Planner also monitors inventory levels and provides feedback to Program leads and their direct Manager regarding expiry and re-supply needs across inventory.
• If required participates in clinical supply group’s system enhancement initiatives, as assigned and needed.
• The clinical supply chain, supply planner, has exceptional communication skills, self-motivated, exposure and/or knowledge of software programs including Microsoft Project, Power Point, MS Project, Interactive Response Technology (IRT), and Microsoft Office.
• Willingness to learn and sense of urgency to meet patient and program needs. Experience with CGMP and/or CGCP is a plus.

Additional Skills & Qualifications:

• Work actively and align with Clinical Operation/Study team to help create forecast for assigned study and program including enrollment rate.
• Support country logistics for shipping and importation, on assigned study or program.
• Monitor regularly drug expiry, and the appropriate inventory levels across assigned clinical programs.
• Support and oversight of packaging requirements for programs and/or protocols assigned
• Monitoring of enrollment, drop-out rates and actual supply need on assigned protocols and/or programs.
• Ensure continuous re-assessment of Project needs, on assigned programs and/or protocols.
• Lead label creation and approvals process, including translations for all countries, on assigned study and/or program responsible for.
• Supports return and destruction of IMPs from sites to depots for assigned study.
• Interface with other members of the Clinical Supply Chain to provide and obtain information and to ensure on time delivery of assigned study.
• Perform inventory checks and manage inventory levels and cycle count at the vendor yearly on assigned study
• Manage temperature excursions during transportation on assigned study

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.