Clinical Research Coordinator (Part-time)

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.

This role is open to candidates working onsite in the Detroit, Michigan area.

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.

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.

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.

• →Perform accurate and timely data entry and maintain study-related records.
• →Collect, process, and prepare clinical research samples in accordance with study protocols and established procedures.
• →Administer and assist patients with study-related questionnaires and assessments.
• →Collaborate with investigators, nurses, and other research staff.
• →Maintain compliance with regulatory and institutional requirements.

• 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 data entry; sample collection and processing, patient questionnaires 

• 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