Clinical Research Physician - w/ focus on either Obesity, Autoimmune Disorders, or Dermatology - (Part Time)
Maitland, FLPart-time
Behavioral Health Market Context
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Benefits
Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hireMedical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered
Qualifications
- •Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role
- •Board certification in area of specialty is required
- •Clinical skills and clinical procedures based on area of specialty
- •Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm)
- •Must possess strong organizational skills, attention to detail, and math proficiency
- •Well-developed written and verbal communication skills
- •3 more items(s)
Responsibilities
- •The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes
- •Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site
- •Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
- •Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
- •Evaluates and assesses participants to ensure only eligible participants enroll into the trials
- •Participates and engages in successful delivery and retention of study participants
- •Interacts positively and collaboratively with sponsors, clients and team members
- •Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs
- •Actively involved in protocol training for staff
- •Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues
- •Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company
- •8 more items(s)