Clinical Research Coordinator

Summary:

For all clinical research studies assigned, the Clinical Research Coordinator (CRC) is responsible for coordinating clinical research studies in a compliant and efficient manner. Under the direction of the Principal Investigator (PI), the CRC will collaborate with all members of the clinical research team to ensure all research initiatives are being met.

Responsibilities:

Management of all duties required for clinical trials from initiation to close-out. Complete research activities including recruitment, screening, enrollment, and supporting patient research participants Keep the Principal Investigator (PI) and leadership informed regarding study operations and progress. Actively identify problems or trends in their development; notify and involve appropriate resources for problem‐solving; recommend procedural modifications or operational improvements and direct implementation and evaluation activities Understanding and adherence to all IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols. Perform phlebotomy and blood specimen collection, processing, and shipment in accordance with study protocols and laboratory procedures. Study activities including coordinating new study activation requirements, screening/enrolling participants, regulatory and compliance requirements, maintaining appropriate study documentation/records, and managing study data.

Additional administrative tasks such as:

invoicing sponsors and reconciling payments, shipping specimen, scheduling procedures and appointments.

Education:

Bachelor's degree and 1-2 years minimum direct experience managing study coordination and regulatory affairs for industry-sponsored clinical trials or equivalent applicable combination of training, education and experience Minimum Qualifications Demonstrated written and oral communication skills Attention to detail Comfortable working both independently (self-guiding) and collaboratively as tasks require Self-motivated, excellent in work planning, time management, organization, and multitasking Familiarity with data entry skills, including Microsoft Office, web/PC-based software Ability to quickly adapt to situations, problem solve, and respond to changing priorities Valid driver's license and reliable transportation - position may require travel Preferred Qualifications Prior experience working with IRB Experience or familiarity with electronic health records Prior experience implementing, developing, and/or leading research programs Experience with contract and budget negotiations This job posting is for a confidential company. Additional details about the organization will be shared during the interview process.

Job Type:

Full-time Pay:

From $55,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Paid time off

Education:

Bachelor's (Required)

Experience:

Clinical Trials:

3 years (Preferred)

Clinical Research:

3 years (Preferred)

License/Certification:

CCRC (Required) Ability to

Relocate:

Richmond, VA 23237: Relocate before starting work (Required)

Work Location:

In person