Join our team of clinical research professionals

We are always seeking Clinical Research Coordinators and Research Associates (Assistant Coordinators) as we continue to expand.  If you have the following experience, send us your resume/CV to:

You will be responsible for the assistance with patient recruitment activities, interviewing / pre-screening and gathering patient information, including medication history. In addition, you will interact with the patients & their families (when needed) to help them gain an understanding and alleviate their apprehension within the studies.

Clinical Research Coordinator (starting pay $14-$16/hr)

  • Patient care experience, Medical Assistant or WV RN Licensed

  • Clinical research experience a plus

  • Excellent organizational and interpersonal skills

  • Great at multi-tasking

  • Prior family/internal medicine experience with various therapeutic areas


Associate Clinical Research Coordinator (starting pay $10-$13/hr.)

Responsible for assisting with the performance of research projects in a clinical setting, including recruitment of potential study subjects, collection and organization of data, scheduling patients for follow up appointments. 


  • Performs data entry for research projects and maintains data bases

  • Maintains study related documents and supplies in the investigator’s office according to ERI’s SOP

  • Ensures accurate and complete compilation of subject data through chart reviews

  • Completes chart reviews of all patients that are potential participants in research studies to ensure they meet eligibility criteria

  • Helps pre-screen potential subjects and help determine eligibility according to the study protocol.

  • Maintains subject enrollment logs for research study

  • Maintains regulatory documents in accordance with ERI SOP and applicable regulations

  • Attends research-related meetings (e.g., site initiation meetings, monitor visits). Communicates as directed with sponsor and team. Completes sponsor-required duties in preparation for study monitor visits.

  • Ensures that all clinical activities are carried out in accordance with the established research protocol and SOPs in compliance with applicable laws, regulations, policies and procedural requirements

  • Performs overall administrative assistance including screening and scheduling patients and other duties as assigned

    • Must have excellent written, oral, interpersonal communication skills, strong organizational skills with attention to detail, intermediate computer skills including Microsoft Excel.



Must have the ability to meet deadlines, work collaboratively as part of a team, continuously exhibit professionalism and adhere to specific study protocol