Description
Clinical Research Coordinator II - Miami, FL (Future Opportunities)
Syneos Health is seeking a Clinical Research Coordinator II to support a clinical trial in Miami, FL. The successful candidate will be responsible for coordinating and performing various study-related activities, including protocol preparation, study conduct, and post-clinic/close-out activities.
Job Responsibilities
- Review and prepare study protocols, informed consent forms, and other study-related documents
- Coordinate study start-up activities, including clinic logistics planning and team training
- Manage multiple clinical trials simultaneously and prioritize tasks effectively
- Collect and enter study data into the appropriate system
- Develop patient rapport and explain research protocols to minimize protocol violations
- Coordinate and monitor screening activities and provide support as required
- Assist with informed consent of study subjects
- Submit data in required timeframe and complete Case Report Forms
- Facilitate audits of study data and respond to inquiries by auditors
- Take the lead and/or overall coordination of clinic activities, including supervising clinic visits and screening eligibility prior to randomization
- Coordinate resolution and/or address QC, monitor, CRF, or other internal/external findings
- Review and/or oversee close-out of study documentation and deviation reporting
Qualification Requirements
- Registered Nurse and/or University Degree such as Bachelor of Science Degree required
- Clinical Research certification preferred
- A minimum of 1 year experience in clinical research required, preferably in coordination of clinical research projects
- Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines
- Required skills: problem solving, planning, and evaluation
- Possess good time management, detail-oriented, and able to multi-task
- Good interpersonal and communication skills with a team focus
- Knowledge of SOP writing and ability to anticipate problems and provide solutions in a timely manner
- Ability to coordinate multiple clinical research projects with competing deadlines
- Proficiency in computer software programs (e.g. Word, Excel, Power Point)
- Proficiency in use of various clinical trial EDC software preferred
Benefits
- Company car or car allowance
- Health benefits, including Medical, Dental, and Vision
- Company match 401k
- Eligibility to participate in Employee Stock Purchase Plan
- Eligibility to earn commissions/bonus based on company and individual performance
- Flexible paid time off (PTO) and sick time