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Travel Clinical Research Coordinator, US Based (Boston, MA)

Care Access

Salary not specified
Aug 12, 2025
Boston, MA, US
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Care Access is looking to revolutionize access to clinical trials for the benefit of patients everywhere by connecting a multi-specialty network of research sites.

Requirements

  • Proficient at ICH/GCP, Good Documentation Practices (GDP), and ALCOA-C+
  • Excellent working knowledge of clinical trials, medicine and research terminology
  • Excellent working knowledge of federal regulations, good clinical practices (GCP), good documentation practices (GDP), and ALCOA-C+
  • Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word, and excel.
  • Proficiency with technology used to support the clinical trial industry. CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc.
  • A minimum of 3 to 4 years Clinical Research experience
  • A minimum of 2 years prior Clinical Research Coordinator experience, management level preferred.

Responsibilities

  • Utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
  • Review and assess protocol, study manuals, and the investigator drug brochure (including amendments) for clarity, logistical feasibility, safety, inconsistencies, etc.
  • Assist PI, Regulatory, Start-up and the Clinical Trial Manager(s) to ensure that all training and study requirements are met prior to trial conduct.
  • Maintain organized file for source documents, patient charts, CRFs, regulatory and study supplies
  • Where appropriate, Investigational Product Accountability: receive, inventory, dispense, monitor patient compliance, and reorder as necessary. Document on accountability log and patient records
  • Collect and evaluate concomitant medications
  • Collect, process, and ship biological specimens as directed by protocol and/or laboratory manual.

Other

  • Extensive travel required. Candidates must be willing to travel 75% of the time nationwide.
  • Ability to communicate and work effectively with a diverse team of professionals
  • Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
  • Critical thinker and problem solver
  • Friendly, outgoing personality; maintain a positive attitude under pressure