Kelly® Science & Clinical is seeking a Clinical Research Coordinator for a contract (temporary) position at a premier client of ours who is a mission-driven leader in advancing medical research, across various locations. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Salary/Pay Rate/Compensation: $28-30/hr depending on experience

Overview:
This company is a pioneering clinical research organization focused on advancing medical research by enrolling diverse populations in high-quality clinical trials. In this role, you’ll collaborate closely with Principal Investigators, research staff, and study participants to support and coordinate clinical trials. This is an opportunity to deepen your research skills, work in a supportive and collaborative environment, and help bring new therapies to patients and families while upholding the highest standards of integrity and excellence.

Schedule:
Normal working hours, onsite, 8-5EST or 9-6PMEST. This role is contracted until the end of 2026 with potential to be hired on permanent basis – NOT guaranteed

Responsibilities:

• Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
  

• Conduct screening visits to collect medical history and other information from study participants
  

• Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines
  

• Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams
  

• Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards
  

• Communicate with study participants to provide education, answer questions, and support adherence to study requirements
  

• Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team
  

• Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines
  

• Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified)
  

• Scan, upload, file, and maintain organized study records and documentation
  

• Apply critical thinking skills to support efficient study operations and problem resolution
  

• Perform other duties as assigned

Qualifications:

• High school diploma or equivalent required</em>; an associate’s degree or higher in a health-related field preferred
  

• Basic knowledge of clinical research strongly preferred
  

• Medical terminology and patient care experience required
  

• Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities
  

• Ability to communicate clearly and professionally with diverse populations
  

• Ability to work collaboratively in a fast-paced, team-oriented environment
  

• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred
  

• Experience with participant screening and the informed consent process strongly preferred
  

• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred