Description
Clinical Supply Specialist Job Description
- Assist in the maintenance and coordination of full drug reconciliation process including review and approval of drug reconciliation records across clinical studies working directly with functional representatives (Clinical, Quality Assurance, etc.) as needed.
- Assist in supply planning and forecasting.
- Interpret protocol information to assist in developing packaging/labeling design and distribution strategy.
- Assist with coordinating the origination, proofing, and translation of clinical study labels as required.
- Manage Temperature excursions affecting clinical trial material.
- Assist in the review of IP documents, electronic document archiving, and quality control.
- Track drug supply at the CMO and clinical sites and maintain current inventory records for IP through the life of the trial to avoid supply issues.
- Track retest updating of clinical trial material.
- Develop templates and SOPs that assist in the management of IP processes.
- Assist Clinical Supplies team with special projects and study-related activities as assigned.
- Manage and assist in Clinical Supply meetings.
- Maintain close communication with internal study teams to ensure study timelines are met and maintain a strong working relationship with Quality Assurance for timely review and approval of study documents.
This is a contract position with a duration of 12 Month(s).
Work Site
This is a hybrid position requiring some days on-site in Princeton, New Jersey and some days remote.
About Actalent
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.
Diversity, Equity & Inclusion
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 actalentaccommodation@ (%20actalentaccommodation@) for other accommodation options.
Compensation Information:
$0.0 / - $0.0 /
Starting At: 0.0
Up To: 0.0
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