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The Opportunity
Description
We're looking for a Manager, Clinical Supply Operations , working in Pharmaceuticals and Medical Products industry in 211 Mt Airy Rd, Basking Ridge, New Jersey, 07920, United States .
Job description:

• Participates in study team meeting, align with study details and collaborates in meeting study objective. Provides supporting information to the teams, in particular RA, RACMC, Clinical ops, and GPMs.
• Designs packaging requirements; based on a general understanding of the technical aspects of packaging in order to evaluate patient kit design and potential solutions to provide patient friendly designs and support of simplified site dispensing approaches.
• Creates drug supply forecast for packaging and labeling operations. Supports patient study needs that consider enrollment rates, country logistics for shipping and importation, drug expiry, inventory re-supply strategy and the appropriate level of inventory per region.
• On-going monitoring of recruitment, drop-out rates and actual supply needs, critical to managing the study needs. Ensure continuous re-assessment of Project needs as recruitment and the study progresses
• Sourcing of comparators and matching placebo as required on a Project by Project basis.

Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20 years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Requirements:

• BS in Pharmacy or related field (MS or PharmD a plus)
• Minimum 5 years of related experience Experience in Project Management, Clinical Supply Management, and/or Pharmaceutical Development required
• Experience and skill in the processes for assimilation and destruction or returned drug supply as well as experience managing third-party contract clinical supply operations required
• Global experience required (member of a team)
• Good knowledge of cGMPs and GCPs across multiple therapeutic areas and possesses general knowledge of blinding approaches and technologies to support various clinical trial designs (randomized, double-blind, double-dummy, placebo-controlled, cross-over, etc.)
• Experienced to manage study needs and possesses the skills and ability to potentially support large phase III Programs.

What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?