Job Title: Clinical Research Coordinator Job Description This position is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and sponsors. The individual will mature in their understanding of research operations and regulations to achieve a fundamental understanding of human subject research. Responsibilities + Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement'. + Complete routine operational activities for multiple research protocols. + Serve as a liaison between site research personnel, industry sponsors, and supervisors. + Collaborate with various site departments, including finance, hospital administrative representatives, and the local IRB if applicable. + Coordinate the schedule of assessments from initial submission of feasibility until study closeout. + Review study design and inclusion/exclusion criteria with the physician and patient. + Ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements. + Ensure the integrity of data submitted on Case Report Forms or other data collection tools through careful source document review. + Monitor data for missing or implausible data. + Create study-specific tools for source documentation when not provided by sponsors. + Collect, complete, and enter data into study-specific case report forms or electronic data capture systems. + Generate and track drug shipments, device shipments, and supplies as needed. + Ensure timely and accurate data completion. + Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations. + Communicate all protocol-related issues to appropriate study personnel or manager. + Attend study-specific on-site meetings, investigator meetings, conference calls, and monthly CRC meetings as required. + Review and respond to any monitoring and auditing findings. Essential Skills + Experience in chart review. + Pre-screening patients. + Experience with clinical trials and clinical research. + Patient recruitment. + Knowledge of CRC and IRB processes. + Experience in clinical study management. Work Environment This role is onsite in Asheville, NC, with shifts from Monday to Friday, 7 am to 4 pm or 8 am to 5 pm. Job Type & Location This is a Contract position based out of Asheville, NC. Pay and Benefits The pay range for this position is $25.00 - $31.00/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 Asheville,NC. Application Deadline This position is anticipated to close on Feb 6, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.