Clinical Research Coordinator II

Location: On-site in Raleigh, North Carolina, USA

Company

hirify.global Wake Research is a US-based network of clinical research sites conducting studies for biopharmaceutical, biotechnology, medical device, pharmaceutical, and clinical research organizations.

What you will do

• Screen and review potential study participants with investigators according to protocol requirements.
• Maintain case report forms, source documentation, study charts, and regulatory records.
• Collect, review, and enter clinical study data accurately.
• Coordinate study start-up, ongoing maintenance, and close-out activities.
• Collaborate with investigators, sponsors, CROs, and internal departments to resolve operational issues.
• Mentor and provide day-to-day oversight to Clinical Research Coordinators and Research Assistants.

Requirements

• At least 2 years of Clinical Research Coordinator experience.
• Extensive clinical trial knowledge through education or experience.
• Ability to interpret complex protocols, follow detailed instructions, prioritize workloads, and multitask.
• Knowledge of GCP guidelines, human subject protection regulations, and HIPAA requirements.
• Strong verbal and written communication, interpersonal, and organizational skills.
• Ability to maintain strict confidentiality of patient, employee, and company information.

Nice to have

• Phlebotomy experience.
• Completed GCP Certification and Advanced CRC training.

Culture & Benefits

• Full-time employment in an on-site clinical research environment.
• 401(k) plan with matching contributions.
• Medical, dental, vision, life, and disability insurance.
• Flexible spending account, employee assistance program, and paid time off.
• Opportunity to contribute to clinical research and healthcare innovation.