Clinical Research Coordinator - not a remote position

Employer Industry: Healthcare

Why consider this job opportunity...
• Opportunity for career advancement and growth within the organization
• Contribute to impactful clinical research that improves community health
• Work within a Magnet-recognized health system known for quality and safety
• Supportive and collaborative work environment with experienced colleagues
• Engage with a diverse range of healthcare professionals and patients
• Comprehensive training and certification opportunities available

What to Expect (Job Responsibilities):
• Coordinate and participate in clinical research studies, ensuring compliance with regulatory processes
• Manage complete and timely data management activities as required by protocol
• Submit documentation and specimens to sponsoring organizations in adherence to protocol specifications
• Assist physicians in documenting and submitting patient adverse events to appropriate authorities
• Coordinate patient study visits, including scheduling, procedures, and data collection

What is Required (Qualifications):
• 2-5 years of data management clinical research experience
• Strong administrative experience and organizational skills
• Excellent communication and interpersonal skills to interact with patients, families, and healthcare professionals
• Required education: High School Graduate; Associate or Bachelor?s degree preferred
• Certification in Human Subjects Protection and willingness to be trained in phlebotomy if needed

How to Stand Out (Preferred Qualifications):
• Certification as a Clinical Research Coordinator (CCRP) or Clinical Research Associate (CCRC)
• Experience with regulatory compliance in clinical research settings
• Familiarity with IRB processes and clinical trial documentation
• Previous experience in a healthcare environment

#Healthcare #ClinicalResearch #CareerOpportunity #DataManagement #HealthcareProfessionals

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