Clinical Research Specialist

Responsible for the management of test materials, staff scheduling and study document archiving. There is a requirement to collaborate with members of the Clinic department in an effective manner to complete assigned tasks. Interpersonal skills are required in order to adequately train other employees to departmental processes and communicate with clients with regards to associated test materials.

• Test Material Management - oversees the receipt, storage & disposition of all study test materials
• Staff Scheduling - assigns weekly clinic duties in accordance with training documentation and employee availability
• Study Archiving - oversees the archiving process of study documentation for completed studies
• Equipment Maintenance - assists the Training & Technical Specialist with equipment calibration & transfer requests
• Training - trains employees on processes owned by the Clinical Research Specialist
• Other duties or tasks assigned by manager

• Bachelor's Degree or 2 years of clinical research experience
• Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
• Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies

job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.

If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.