What are the responsibilities and job description for the Clinical Research Coordinator position at Edward Jenner Medical Research?
Company Description
Edward Jenner Research Group LLC.
Role Description
This is a full-time on-site role located in Fort Lauderdale, FL, for a Clinical Research Coordinator. The role involves managing clinical trials and research studies, ensuring compliance with study protocols, and obtaining informed consent from participants. Responsibilities include coordinating study operations, monitoring patient enrollment and progress, collecting and managing data, and collaborating with research teams to meet project goals.
Qualifications
- Proficiency with Informed Consent processes and Protocol adherence
- Hands-on Clinical Research Experience, particularly with clinical trials
- Strong background in Research methodologies and practices
- Exceptional organizational, problem-solving, and critical thinking abilities
- Effective written and verbal communication skills
- Experience in healthcare or medical settings is an advantage
- Must have 2 years experience in clinical research industry