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Fast Growing Pharmaceutical Company is looking for:

POSITION: Assistant Clinical Manager, BE Studies

SALARY: $100-115k + BONUS

LOCATION: Caldwell New Jersey Area

EXPERIENCE: Experience with Biologicals Research, Bioequivalence Studies, and adherence to GLP and GCP guidelines

RELOCATION: Relocation Assistance

The Manager is responsible for the set-up and implementation of clinical BE trials for US projects. Ensures that bioequivalence (BE) studies sponsored are conducted and data is generated, documented and reported in compliance with the study protocol, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and the applicable regulatory requirements in the country where the study is to be conducted. Provides administrative and logistical support, as required. Follows up on current guidance and regulatory requirements related to conduct of BE studies/clinical studies.


University degree in the field of Pharmaceutical Sciences, Pharmacy, Chemistry, Health and Science.

MS Degree - 8-10 Years Relevant Experience, PhD 4+ Years Relevant Experience

Ability to multi-task and manage several projects in parallel, paying attention to detail.

Ability to be proactive in identifying issues and hurdles that may handicap the effective implementation of the trial and resolve the issues in a timely fashion

Good project planning, negotiation and presentation skills.

Good project management skills

Excellent interpersonal and verbal/written communication skills.

Ability to forge cross-functional working relationships with internal teams and external partners.

Ability to resolve routine issues effectively and independently.

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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