Clinical Research Lead

6 days ago

West Des Moines, Iowa, United States Eximia Research Full time
Job Title: Lead Clinical Research Coordinator

Eximia Research is a leading provider of clinical research services, with a network of premier investigational sites across the country. We are seeking a highly skilled and experienced Lead Clinical Research Coordinator to join our team.

Job Summary:

The Lead Clinical Research Coordinator will serve as the subject matter expert and leader of a clinical trial team, responsible for conducting and managing clinical trials from start-up through study close-out. The successful candidate will have a strong background in clinical research, excellent leadership and communication skills, and the ability to work effectively in a fast-paced environment.

Key Responsibilities:
  • Lead a study team to execute clinical trials, ensuring compliance with study protocols, GCP, and Eximia Research SOPs
  • Mentor and train staff in clinical trial conduct, protocol requirements, and communication skills
  • Develop and implement training strategies and mitigation plans
  • Conduct and manage clinical trials, including start-up, vendor management, subject recruitment, and data management
  • Apply project management concepts to manage risk and improve quality in clinical research studies
  • Develop and coordinate research and administrative strategies to successfully manage assigned protocols
  • Communicate effectively with coworkers, leadership, study subjects, sponsors, CROs, and vendors
  • Ensure good documentation practices and confidentiality of patient and sponsor information
  • Develop communication and escalation strategies to ensure patient safety and compliance with regulations
Requirements:
  • Bachelor's degree and 8 years of experience as a Clinical Research Coordinator, or equivalent combination of education and experience
  • Advanced knowledge of medical terminology and proficiency in Microsoft Office software
  • Excellent verbal, written, and organizational skills, with ability to work in a fast-paced environment
  • Ability to work independently, plan and prioritize multiple deliverables, and adapt to changing circumstances
  • Certified Clinical Research Coordinator (CCRC) certification preferred
Physical Demands:
  • Sit or stand for long periods of time
  • Travel locally and nationally
  • Communicate in person and by phone
  • Limited to moderate walking required
  • Limited to lifting up to 30 pounds

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