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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
11 Mei 2026
Deadline
11 Mei 2027

Job Description

Join Boston Medical Center's pioneering clinical research division as a Clinical Research Coordinator. Shape the future of medicine by managing pivotal trials in our state-of-the-art facilities. This role offers unparalleled opportunities to collaborate with leading researchers while advancing patient care through innovative therapies.

Our dynamic environment combines cutting-edge technology with compassionate patient-centered care, providing a platform for professional growth and meaningful impact. You'll work with multidisciplinary teams in a culture that values scientific rigor and ethical excellence.

Responsibilities

  • Oversee clinical trial protocols from initiation to closure, ensuring FDA/ICH/GCP compliance
  • Manage participant recruitment, screening, and retention strategies
  • Coordinate data collection, monitoring, and regulatory documentation
  • Liaise with IRB, sponsors, and investigative sites for protocol adherence
  • Maintain electronic Case Report Forms (eCRFs) and study databases
  • Train clinical staff on trial-specific procedures and safety protocols
  • Analyze interim data and prepare study reports for sponsors

Qualifications

  • Master's degree in Clinical Research, Nursing, or Life Sciences required
  • Certified Clinical Research Professional (CCRP) preferred
  • 3+ years clinical trial coordination experience in therapeutic area
  • Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
  • Deep knowledge of 21 CFR Part 11 and ICH-GCP guidelines
  • Exceptional organizational skills with attention to regulatory detail
  • Strong written/verbal communication and stakeholder management
  • Ability to manage multiple competing priorities in fast-paced settings

Required Skills

Clinical Trials Regulatory Compliance Data Management EDC Systems FDA Regulations Patient Recruitment Protocol Development IRB Coordination

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