Clinical Research Coordinator (Part-time)

Advarra; Detroit, Northern (MI, KY); Hybrid; USD 34,000 - 55,000; Part time

Job summary

Advarra is seeking a part-time Clinical Research Coordinator to support clinical studies in Detroit, Michigan. You will assist with data collection, participant consenting, and study documentation, ensuring adherence to protocols and regulatory standards.

This onsite role requires a Bachelor's with 3+ years or an Associate with 4+ years, phlebotomy experience, and solid data-entry skills; preferred CCRP/CCRC/SOCRA certifications.

Qualifications

• Bachelor’s degree with 3+ years of relevant experience.
• Associate’s degree with 4+ years of experience.
• Experience in phlebotomy and handling clinical specimens.
• Experience with data entry and study documentation.
• CCRP/CCRC/SOCRA or equivalent preferred.

Responsibilities

• Perform accurate data entry and maintain study records.
• Collect, process and prepare clinical research samples per protocols.
• Administer and assist with patient questionnaires and assessments.
• Collaborate with investigators, nurses and research staff.
• Maintain regulatory and institutional compliance.

Skills

Interpersonal skills

Communication skills

Organizational skills

Education

Bachelor's + 3+ yrs

Associate + 4+ yrs

CCRP

CCRC

SOCRA

Job description

Clinical Research Coordinator (Part-time)

Job Category: Review Services

Requisition Number: REVIE004677

• Posted : September 1, 2026
• Part-Time
• On-site

Locations

Showing 1 location

Michigan, USA

Description

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Location

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

Job Duties & Responsibilities

• 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.

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 data entry; sample collection and processing, patient questionnaires

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.