Clinical Supply Chain Associate job in Cambridge, USA

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Supply Chain, Procurement/Purchasing, Planning

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a Clinical Supply Chain Associate with a leading pharmaceutical company in Cambridge, MA. Successful candidates will hold experience in logistics, inventory, and clinical supplies.

Job Responsibilities:

Support programs and protocols, in tandem with program leads; packaging, labeling, shipment and drug return logistical activities by interacting with internal and external customers and suppliers in order to accomplish project objectives.
Manage and maintain IMP distribution and returns drug plans and manage Clinical Supplies Documentation associated with assigned program, to maintain GMP.
Monitor inventory levels and provides feedback to {Program leads and their direct Clinical Supply Manager regarding expiry and re-supply. If required participates in Clinical Supplies group developmental initiatives, as assigned and needed.
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 re-supply for assigned clinical programs.
Support packaging requirements for programs and/or protocols assigned.
Monitor 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.
Drive label creation and approvals process, including translations for all countries, on assigned study and/or program responsible for.
Support 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.

Skills and Requirements:

Must have exceptional communication skills, exposure and/or knowledge of programs including Microsoft Project, Power Point, MS Project, 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.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Nadine Rucci at (+1) 215-531-5281 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#LI-ND2

#Commercial