• Clinical Research Coordinator Part-time - ATL

    Actalent (Norcross, GA)


    Job Title: Clinical Research Coordinator (Part-Time) - ATL

    20 hours per week

     

    Must have CRC experience within the last 6 months

    Job Description

    In this role, you will be responsible for coordinating clinical research studies, including study start-up, patient recruitment, and providing backup support as needed.

    Responsibilities

    + Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.

    + Coordinate the operational aspects of new and ongoing clinical trials at the site.

    + Work under the supervision of Principal Investigator(s), exercising excellent clinical judgment in patient monitoring and care.

    + Maintain daily contact with Principal Investigator(s) for recruitment activities, study start-up, and general daily communication.

    + Ensure protocol execution and proper delegation and training of staff working on any given protocol.

    + Conduct patient recruitment and pre-screening.

    + Maintain and submit IRB communications and regulatory documents.

    + Communicate timely with internal teams, investigators, review boards, and study subjects.

    + Prepare study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs.

    + Perform other duties as assigned.

    Essential Skills

    + Experience in patient recruitment, clinical trials, and clinical research.

    + Proficiency in Good Clinical Practice (GCP).

    + Skills in phlebotomy and understanding of weight loss procedures.

     

    Additional Skills & Qualifications

     

    + A minimum of a High School Diploma is required.

    + Prior experience with Electronic Data Capture (EDC) systems is required.

    + Experience in Endocrinology/Diabetes trials is preferred but not mandatory.

    + Strong management and organizational skills, with an understanding of medical procedures.

    + Exceptional interpersonal skills and the ability to work independently.

    + Capability to lift a minimum of 50 pounds.

    + Proficiency in professional and Business English, both written and spoken.

     

    Work Environment

     

    This position is on-site and patient-facing within a clinic environment, providing an opportunity to engage every healthcare professional in clinical research and to make clinical trials a care option for every patient.

     

    Job Type & Location

     

    This is a Contract position based out of Norcross, GA.

    Pay and Benefits

    The pay range for this position is $25.00 - $32.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Norcross,GA.

     

    Application Deadline

     

    This position is anticipated to close on Jan 10, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.