About this role
Description
If you are already in our network, do not fill out this form. If you are not part of our network, please register using the Expert Enrollment Form to be considered.
Location
This role is open to candidates working onsite in the New Brunswick, New Jersey 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 will be responsible for patient appointment coordination, collaboration with clinical technicians, study data entry management, and support study enrollment. This role will ensure adherence to study protocols and regulatory standards while contributing to the success of clinical operations.
Job Duties & Responsibilities
- Perform accurate and timely data entry and maintain study-related records.
- Coordinate patient appointments and facilitate clinical trial visits
- Support study enrollment and follow-up/closeout activities
- Collaborate with coordinators, clinical technicians, clinical research lead, and other research staff.
- Maintain compliance with regulatory requirements
Basic Qualifications
- Bachelor's degree with 3+ years of relevant experience OR associate's degree with 4+ years of experience.
- Demonstrated experience in phlebotomy and with collecting, processing, labeling, storing, and preparing clinical specimens for shipment.
- Demonstrated experience with patient scheduling, visit coordination, EDC data entry, and regulatory documentation.
Preferred Qualifications
- Strong interpersonal and client interaction skills with ability to independently manage multiple clinical trials
- Strong communication and organization skills
- Ophthalmology/retina clinical research experience strongly preferred
- GCP and IATA certification required (dry ice specimen handling/shipping).
- Certified Clinical Research Professional (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) or equivalent preferred