Clinical Research Coordinator - Ophthalmology

Come work with a growing, multi-site clinical research team!

CLINICAL RESEARCH COORDINATOR

PURPOSE

To work as an integral member of the Rovia/Investigator site staff, maintaining the day-to-day operations and assist in the development of the Rovia network. This includes planning, coordinating, and executing clinical studies in accordance with the protocol, contracted scope of work, ICH/GCP, Sponsor, CRO, and Rovia SOPs and any relevant local guidelines and regulations.

Candidates for this role must have ophthalmology experience and the ability to travel locally to be considered.

Responsibilities

Work directly as the patient/subject interface at research sites to deliver high-quality patient data in accordance with local regulations, agreed scope of work and as required by protocol.

• Attend and participate in investigator meetings, monitoring visits, audits, seminars and other regional or national meetings.
• Assist with screening and enrollment of subjects into assigned studies.
• Exhibit excellent customer service skills with trial subjects to encourage retention and future recruitment.
• Assist with the establishment of a recruitment and contingency plan for each study.
• Perform functions necessary for successful completion of all required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation and organizational tasks, where appropriate and as delegated by the investigator, in accordance with local county requirements.
• Complete source documents and case report forms accurately in both paper and electronic format.
• Assist investigator with recording and reporting of adverse events and SAEs per local regulatory authority guidelines.
• Perform other duties as assigned.
  
  
  

Required Knowledge, Skills And Abilities

• Sound knowledge of medical terminology.
• Sound knowledge of ICH/GCP and Regulatory requirements.
• Excellent interpersonal and organizational skills.
• Proficient in the use of Microsoft Office and Excel.
• Fluent in written English language.
• Ability to work independently and in a team environment.
• Ability to maintain confidentiality.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  
  
  

Minimum Required Education, Experience And Certifications

• Bachelor’s degree or equivalent experience
• Minimum of 2 years in clinical research
• Ophthalmology experience required
• Phlebotomy capabilities strongly preferred
• Current CPR certification – can be provided upon hire
• International Air Transport Association (IATA) Certification – can be provided upon hire
• Good Clinical Practice (GCP) - can be provided upon hire
  
  
  

Job Type: Full-time

Benefits:

• Paid time off
• Flexible schedule
• Advancement opportunities
• 401(k) with company match
• Health, dental, and vision insurance
• HSA with company match
• Life and disability coverage
• Employee referral program
• Referral program
  
  
  

Schedule:

• Day shift
• Monday to Friday
  
  
  

Work Location: Primarily onsite at 11512 Lake Mead Ave, Suite #534, Jacksonville, FL 32256. Candidate must be willing to commute to multiple locations in the Jacksonville area.