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Health Care 🏢 Full Time ⭐️ Verified

Clinical Research Coordinator

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

Job Description

Join Boston Medical Center's pioneering clinical research division and drive transformative healthcare breakthroughs. We're seeking a meticulous Clinical Research Coordinator to manage complex clinical trials while ensuring regulatory compliance and patient safety. This role offers the opportunity to work alongside world-class physicians in a cutting-edge environment where your contributions directly impact patient care and medical innovation.

Boston Medical Center is a leading academic medical center committed to providing exceptional care to diverse communities. We offer competitive benefits, professional development opportunities, and a collaborative culture that values innovation and excellence.

Responsibilities

  • Oversee end-to-end management of clinical trials including protocol development, IRB submissions, and regulatory compliance
  • Recruit, screen, and enroll study participants while maintaining strict adherence to GCP standards
  • Coordinate data collection, management, and analysis using electronic systems (e.g., REDCap, Medidata)
  • Monitor adverse events and ensure timely reporting to regulatory bodies and sponsors
  • Liaise with multidisciplinary teams including physicians, nurses, and biostatisticians
  • Maintain accurate study documentation and prepare regulatory submissions
  • Train clinical staff on trial protocols and research procedures

Qualifications

  • Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Minimum 3 years experience in clinical research coordination with therapeutic area focus
  • Expertise in FDA regulations, ICH-GCP, and protocol development
  • Proficiency in clinical trial management systems and data management tools
  • Exceptional organizational skills with attention to detail and documentation accuracy
  • Strong communication abilities for stakeholder interactions and patient education
  • Experience with complex oncology or cardiovascular trials preferred

Required Skills

Clinical Research Regulatory Compliance Data Management GCP IRB Submissions Clinical Trials REDCap Patient Recruitment FDA Regulations Protocol Development

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