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Regulatory Affairs Senior Associate Full Time

We require an experienced Regulatory Affairs Senior Associate to join our expanding team in our office located in Bedminster NJ. ...

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Project Manager (PMO)

JOB SUMMARY: For day-to-day project operations, regulatory support and administrative activities either on-site at the office or at other locations, ...

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Director of Biostatistics Contract

As a specialty pharma in the field of oncology our client is committed to creating anticancer drugs with diverse mechanisms ...

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Strategic Accounts Director Full Time

The Strategic Account Management Director is a consultative sales position focused on the life science sector including large pharmaceutical and ...

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eMed Coordinator Contract

Responsible for managing the Medical, non-promotional, material review process for our client using Pharma eMED system (Aprimo).  Working with program ...

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Clinical Data Manager Contract

Main Purpose of Job: Ensure quality and timely clinical data delivery for multiple US local Phase IVc studies outsourced to ...

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Clinical Trial Lead Contract

One of our large pharma clients is recruiting for a Clinical Trial Lead in Morristown New Jersey. A global healthcare ...

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Project Manager Contract

A top pharma company is looking for experienced project managers, you will need to be able to think outside the ...

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Publications Lead / Scientific Team Leader Full Time

Our client in who has offices in New York and New Jersey is looking for an experienced publication professional to ...

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Associate Director, Regulatory Affairs Full Time

Position Summary:      Under the leadership of the Director/Senior Director, CMC Regulatory Affairs the incumbent manages the global regulatory CMC activities except ...

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