Coordinate Clinical Studies adhering to the principles of Good Clinical Practice
Collect initial medical background from patients and other appropriate sources
Work as a cohesive team member coordinating assigned studies and backing up other studies on location
Educate and provide information to patients, families, and community groups regarding clinical drug trials
Assist and support Recruitment Team with prescreen activities and other activities related to subject recruitment
Attend Study related training and site initiation meetings
Inventory, handle, and maintain accountability for all study supplies and investigational products
Facilitate study monitoring visits and prompt resolution of all study related queries
Maintain professional and appropriate interactions with sponsors and all other study related personnel, subjects, families, and Meridien staff members.
Assume responsibility for an on-call rotation for after hour needs of subjects, sponsors, and families as needed.
Other duties as assigned
An excellent, comprehensive benefits package is available that includes:
Three levels of medical plans with dependent coverage available
Dental, Vision, and Supplemental benefit plans
Voluntary life and AD&D for you and your dependents
Company paid Basic Life and AD&D, Short-term and Long-term Disability
401(k) Retirement plan with company match and immediate vesting
Paid time off and holidays with no waiting period
Meridien Research is an Equal Opportunity Employer/Drug-Free Workplace/Smoke-Free Workplace . Visit www.newstudyinfo.com to learn more about Meridien Research.
Qualifications and Skills
Positive candidate must possess the following:
Commitment to excellence and quality patient care
High organizational ability with strong attention to detail
Excellent phlebotomy and IV skills
Critical thinker and problem solver
Intermediate computer skills needed
Education Requirements: Minimum 2 year degree necessary
License: active Florida RN license mandatory
Experience: Clinical research experience preferred but we will train the right candidate
The Clinical Research Coordinator will work under a Site Director and Principal Investigator/Physician.
Please submit a resume, cover letter and CV when responding.
About Meridien Research, Inc.
Meridien Research has been offering medical research to residents of Central Florida (specifically the Tampa Bay area) since 2000. With six privately-owned clinical trial facilities in St. Petersburg, Tampa, Maitland, Spring Hill, Bradenton and Lakeland, Florida, Meridien Research’s mission is to provide consistent, high-quality clinical research in a professional, ethical and timely manner.
We have conducted more than 2,000 clinical trials across a wide range of therapeutic areas in the pharmaceutical, biotechnology and contract research industries. Meridien Research’s investigators are board certified and specialists in endocrinology, dermatology, internal medicine, cardiology, central nervous system disorders and men’s and women’s health. Our CTMS database includes 100,000+ diverse patients.
Meridien Research’s services include phase Ib-IV and PK and specialty studies, dedicated marketing and patient recruitment, rapid feasibility response and streamlined communication, contracts and invoicing. With medical research facilities located in Central Florida, we bring medical research close to home for millions of people.