Clinical Research Coordinator

Careerscape

Boston, MA

JOB DETAILS
SALARY
$58,000–$72,000 Per Year
JOB TYPE
Full-time
SKILLS
Academic Background, Academic Research, Adverse Events, Biology, Case Report Form (CRF), Certified Clinical Research Coordinator (CCRC), Clinical Information Systems, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Data Collection, Dental Insurance, Detail Oriented, Disability Insurance, Documentation, Electronic Data Capture (EDC), Employee Assistance Plan, FDA Requirements, GCP (Good Clinical Practices), Healthcare, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Inventory Management, Investigational New Drug (IND), Life Insurance, Medical Research, Microsoft Office, Nursing, Organizational Skills, Presentation/Verbal Skills, Product Management, Regulations, Regulatory Compliance, Regulatory Requirements, Startup, Time Management, Vision Plan, Writing Skills
LOCATION
Boston, MA
POSTED
1 day ago

Our client, a healthcare research company based in Boston's Longwood Medical Area, is hiring a Clinical Research Coordinator to support the day-to-day operations of ongoing clinical trials. This role works closely with principal investigators, sponsors, and study participants to ensure trials are conducted in compliance with protocol requirements and regulatory standards.

The coordinator will manage participant recruitment, informed consent, data collection, and documentation across multiple concurrent studies. This position requires close attention to detail, strong organizational skills, and the ability to work within a fast-paced academic medical research environment.

This is a full-time, on-site role suited for someone with prior clinical research or healthcare experience who is looking to grow within a structured research organization.

Responsibilities

  • Coordinate all phases of assigned clinical trials from startup through closeout
  • Screen, recruit, and consent study participants according to protocol
  • Maintain accurate case report forms and source documentation
  • Schedule and conduct participant visits and follow-up assessments
  • Track and report adverse events to the appropriate regulatory bodies
  • Prepare study materials and documentation for sponsor and IRB audits
  • Manage investigational product inventory and accountability logs
  • Communicate study status updates to principal investigators and sponsors

Requirements

  • Bachelor's degree in life sciences, nursing, or related field
  • Minimum 2 years of clinical research or healthcare experience
  • Working knowledge of GCP and FDA regulatory guidelines
  • Experience with electronic data capture systems
  • Strong written and verbal communication skills
  • Ability to manage multiple studies and competing deadlines
  • Proficiency with Microsoft Office and clinical trial management software
  • CCRC or CCRP certification preferred

Benefits

  • Medical, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and holidays
  • Tuition reimbursement for continuing education
  • Professional development and certification support
  • Life and disability insurance
  • Employee assistance program
  • Commuter benefits

About the Company

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Careerscape