Job Summary:
We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. The Clinical Research Associate will be responsible for assisting in the coordination and execution of clinical trials, ensuring compliance with regulatory guidelines and protocols. This opportunity is not a remote position and is on-site. This is a great opportunity for a candidate who has a background in the medical field (CNA, MA, EMT) to advance their career!

ESSENTIAL FUNCTIONS

• Assists the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation, and patient chart review to determine eligibility for enrollment in current and upcoming studies along with scheduling potential patients.

• Assists the clinical team with site follow-up of documents and reports.

• Assists with accurately updating and maintaining clinical systems that track compliance and performance within project timelines according to ICH-GCP and local regulations.

• Assist the coordinator with clinical study start-up and support, including but not limited to essential document collection and IRB submission.

• GCP Certification or willingness to become certified.

• Ability to assist in patient visits per study protocols.

ECWC offers competitive compensation packages including benefits such as health and dental insurance, short-term disability coverage, retirement plan/401K, and paid time off. Join our team today and contribute to groundbreaking research that will shape the future of healthcare.

Job Type: Full-time

Pay: $37,000.00 - $44,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Free parking
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Medical specialties:

• Ob/Gyn

Physical setting:

• Office

Schedule:

• 8 hour shift

Ability to Commute:

• New Bern, NC 28562 (Preferred)

Work Location: In person