Clinical Research Scientist

A client of ours in Florham Park, NJ is looking for a clinical research scientist to join their team. This individual will be responsible for managing clinical and non-clinical studies and assist with inventory management, labeling, returns and tracking shipping of clinical test materials. They will be responsible for completing detailed review of study-related documents which may include, but are not limited to, protocols, study reports, informed consent forms, and case report forms. This individual will also work closely with the scientific affairs team to develop new clinical studies and protocols. They will review, write, or revise SOPs and ensure all documentation is accurate and filed in accordance with SOPs.

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Required Skills & Experience
- 1-3+ years of experience within clinical research monitoring specific
- Knowlege of GCPs
- Experience reviewing case report forms
- Experience reviewing protocols and informed consents
- Willing to travel (clinical sites, NJ, PA, NC, FL, AZ) few times a year
- Experience within CPG or pharmaceuticals

Nice to Have Skills & Experience
- GCP certified
- Cosmetic experience

Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.