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Clinical Research Coordinator

Boston Medical Center
Boston
Salary Estimate
USD 85.000 – USD 110.000
Latest
Live Update
19 Mei 2026
Deadline
19 Mei 2027

Job Description

Join Boston Medical Center's groundbreaking research division where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive critical medical studies that shape the future of patient treatment. As part of our dynamic team, you'll collaborate with world-class physicians, manage complex trial protocols, and contribute directly to life-changing discoveries.

Our state-of-the-art research facilities offer unparalleled resources, and our commitment to professional development ensures continuous growth. This hybrid role combines impactful clinical work with the opportunity to publish findings in leading medical journals.

Responsibilities

  • Manage complex clinical trial protocols from initiation to closeout, ensuring strict FDA and GCP compliance
  • Recruit, screen, and enroll eligible participants while maintaining ethical standards and patient confidentiality
  • Coordinate multi-disciplinary research teams, including physicians, nurses, and biostatisticians
  • Maintain accurate electronic data capture systems and conduct rigorous source document verification
  • Prepare regulatory submissions and ensure timely IRB approvals and renewals
  • Analyze preliminary data and draft interim reports for sponsor review
  • Train clinical staff on protocol-specific procedures and regulatory requirements

Qualifications

  • Bachelor's degree in Nursing, Health Sciences, or related field (Master's preferred)
  • 3+ years clinical research coordination experience in hospital or academic setting
  • Certified Clinical Research Professional (CCRP) or equivalent certification
  • Expertise in FDA regulations, ICH-GCP guidelines, and HIPAA compliance
  • Proficiency with electronic data capture systems (e.g., REDCap, Medidata Rave)
  • Exceptional organizational skills with ability to manage multiple concurrent trials
  • Strong written and verbal communication skills for stakeholder interactions
  • Experience with oncology or cardiovascular trials highly desirable

Required Skills

Clinical Research Regulatory Compliance Data Management IRB Submissions Protocol Development Patient Recruitment FDA Regulations Electronic Health Records

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