Jr Clinical Research Coordinator

Job Description

As the Medical - Technical Assistant (Clinical Research), you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations.

You will meet with healthy, paid panelists for hands-on consumer product efficacy and safety testing, including applying sunscreen or other products to the skin.

Are you a health care services professional ready for a challenge in a new environment?

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Sets up and conducts studies in compliance with the protocol, SOPs, applicable regulations, and GCPs.

Prepares, completes, organizes, and maintains all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study-specific documents.

Performs station and instrumentation duties on other studies as assigned, including the collection and recording of clinical information.

Reviews and provides feedback on draft protocols, recruiting materials, and draft clinical study reports.

Coordinates scheduling subjects for visits and orders checks for subject compensation.

Responds to queries from Quality Assurance and Statistics Departments.

Prepares and is accountable for all Test Material for managed studies.

Provides excellent customer service to clients and panelists and maintains positive interaction with peers and supervisors.

Completes other duties or tasks assigned by the Clinic Manager and/or Supervisor.

This job operates in a professional office and clinic environment.

This role routinely uses standard office equipment such as computers and phones and clinical bioinstrumentation.

Adheres to internal standards, policies, and procedures.

Performs other duties as assigned.