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Health Care 🏢 Full Time ⭐️ Verified

Senior Clinical Research Coordinator

MedTech Innovations Group
Boston
Salary Estimate
USD 85.000 – USD 110.000
Live Update
16 Mei 2026
Deadline
16 Mei 2027

Job Description

Join our pioneering team at MedTech Innovations Group, where we're revolutionizing patient care through cutting-edge clinical research. As a Senior Clinical Research Coordinator, you'll lead pivotal trials that shape the future of medicine in our state-of-the-art Boston facility. We offer a collaborative environment where your expertise directly impacts healthcare innovation, with comprehensive benefits including health insurance, retirement plans, and professional development opportunities.

Our ideal candidate thrives in dynamic, mission-driven settings and possesses a deep commitment to ethical research practices. You'll work alongside world-class physicians, scientists, and regulatory experts to ensure trials meet the highest standards of scientific integrity and patient safety.

Responsibilities

  • Oversee end-to-end management of Phase II-III clinical trials, including protocol development, site selection, and regulatory compliance
  • Lead cross-functional teams of 5+ clinical professionals to execute study protocols with 95%+ accuracy
  • Implement innovative data capture systems using EDC platforms (e.g., Medidata Rave) ensuring 99% data integrity
  • Manage complex budgets and vendor relationships for multi-center studies with $1M+ annual spend
  • Mentor junior coordinators while maintaining 100% audit-ready documentation
  • Present trial outcomes to FDA investigators and internal ethics committees

Qualifications

  • Master's degree in Clinical Research, Public Health, or related field with 5+ years trial coordination experience
  • Certified Clinical Research Professional (CCRP) or equivalent certification required
  • Proven expertise in oncology or neurology therapeutic areas with 3+ phase III trials
  • Advanced proficiency in EDC systems and regulatory databases (e.g., ClinicalTrials.gov)
  • Exceptional project management skills demonstrated through successful multicenter trial leadership
  • Strong analytical abilities with experience in SAS or R for statistical data interpretation
  • Excellent interpersonal skills with demonstrated ability to manage investigator relationships

Required Skills

Clinical Research Regulatory Compliance EDC Systems Protocol Development Budget Management Team Leadership Data Integrity FDA Regulations Oncology/Neurology SAS/R

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