Clinical Research Coordinator (Part-time/Onsite)

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advarraRaleigh (NC)

Clinical Research Coordinators Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

SENIORITY

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About the role

Clinical Research Coordinator (Part-time/Onsite) Locations Showing 1 location North Carolina, USAOn-site Review Services Part-Time Requisition #: CLINI004784Description Location This role is open to candidates working onsite in the Wilmington, North Carolina area. Company Information At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact. Company Culture

Our people: --both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision.

Our values: (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Job Overview: Summary The part-time Clinical Research Coordinator supports clinical research projects through data collection, participant consenting, and study documentation. This role will ensure adherence to study protocols and regulatory standards while contributing to the success of clinical operations. The Coordinator must be available to work onsite and have ophthalmology experience.

Job Duties & Responsibilities: Obtain informed consent and maintain accurate study documentation. Coordinate and collect data in accordance with study protocols. Collaborate with investigators, nurses, and other research staff. Maintain compliance with regulatory and institutional requirements.

Basic Qualifications: Bachelor’s degree with 3+ years of relevant experience OR associate’s degree with 4+ years of experience.

Preferred Qualifications:

Strong interpersonal and client interaction skills
Strong communication and organization skills
Certified Clinical Research Professional (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) or equivalent preferred

Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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