Highmark Health

Clinical Research Coordinator - Full Time - Day Shift - AGH

Pittsburgh PA, 15212, 320 E N Ave · Full-time

Sponsorship not specifiedDetected 5 days ago

ComplianceAccessibilityHIPAAClinical TrialsClinical ResearchResearch

About the role

This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources.
Maintains compliance with all regulatory bodies associated with human subject research.

Collects, maintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies. (15%)
Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies. (15%)

Associate's degree, RN, or equivalent research experience.
1-3 years' related experience.
Bachelor's Degree.
Driver's license may be required depending on facility requirements.
It may not contain a comprehensive inventory of all duties, responsibilities, and qualifications required of employees to do this job.
As a component of job responsibilities, employees may have access to covered information, cardholder data, or other confidential customer information that must be protected at all times.
Performs other duties as assigned or required. (10%)
Completes required follow-up and active patient monitoring per study protocol. (30%)
Current research-related certification from accredited program such as The Association of Clinical Research Professional (ACRP), e.g. Certified Clinical Research Coordinator (CCRC), ACRP Certified Professional (ACRP-CP) or The Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professionals (CCRP).

Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study. (30%)
Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent.

For accommodation requests, please contact HR Services Online at HRServices@highmarkhealth.org

aintains, and stores all relevant clinical data, case report forms, and regulatory binders in accordance with the study sponsor and all regulatory bodies

This listing is sourced directly from Highmark Health's careers page and normalized into a canonical job model.