Principal Scientist managing analytical projects for Hikma Pharmaceuticals focusing on compliance and validation in pharmaceutical development. Overseeing technical projects and mentoring team members.
About the role
- Laboratory Research Assistant conducting data collection for clinical device trials at UHS locations in New York. Responsible for maintaining data integrity and compliance with research protocols.
Responsibilities
- Collect data for clinical device trials and specimen procurements
- Prepare and maintain regulatory forms and records
- Ensure quality and integrity of clinical data through eCRF database and on-site source verification
- Participate in site sponsor visits, trainings, and inspections
- Contribute to the development of workflow procedures
- Maintain trial data files in compliance with protocol requirements
Requirements
- High school diploma and at least 1 year of experience working in health care
- Associate degree in scientific discipline or health care field preferred
- Direct experience working with patients in a healthcare setting preferred
- Knowledge of basic medical terminology and clinical skills
- Proficient with Microsoft Office, general computer systems, and ability to learn other applications as needed
- Excellent written and verbal communication skills
- Good customer service skills
- High level of organization, ability to multitask, ability to work as a team and independently
Benefits
- This position is not eligible for benefits.
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