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Clinical Research Physician/Investigator

Suncoast Skin Solutions
Brandon, Florida
Closing date
Oct 2, 2024

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Full Time
Position Type

Qualified candidates must have dermatologist experience and clinical trial investigator experience.

Role and Responsibilities


  • Serve as Principal Investigator or Sub-Investigator on assigned clinical trials
  • Provide medical monitoring for clinical studies
  • Responsible for the safety and well-being of the volunteer subjects
  • Acts as part of a multidisciplinary team to provide continuity of care to patients throughout various stages of treatment on protocol and follow-up
  • Prepare clinical development plans and institute properly approved clinical protocols
  • Contribute and support department/clinical initiatives to improve the quality and content of all clinical programs
  • Provide medical expertise to Clinical Operations activities for safety amendments
  • Responsible for the performance, quality and oversight in clinical trials
  • Assist in preparation of abstracts, manuscripts and presentation for meetings
  • Conduct and assess clinical safety and efficacy data and write clinical study reports
  • Coordinate and provide medical training including indication training, protocol training, safety presentations for clinical staff, project teams, or during meetings
  • Provide input for weekly status reports
  • Review and approve protocols, case report forms, informed consent forms, and other study documentation
  • Review and approve final study reports or other clinical documents
  • Ensure optimal study conduct
  • Assist in organization, coordination, and execution, as required, of internal and external meetings
  • Actively contribute to developing and reviewing Standard Operating Procedures and Working Instructions in the role of process owner and subject matter expert
  • Actively contribute to the validation and implementation of new systems, instruments methods and assessments
  • Lead and actively participate in the training and coaching of on-call staff and new and less experienced colleagues
  • Support medical affairs activities involving product evaluation, labeling and surveillance


  • Demonstrates initiative and responsibility
  • Able to perform repetitive tasks without loss of focus
  • Adheres to ethical principles
  • Time Management
  • Adapts to change
  • Attends all team meetings and mandatory in-service training/education


  • Recognizes and respects cultural diversity
  • Adapts communication to individual s ability to understand
  • Uses professional, pleasant telephone etiquette
  • Uses medical terminology appropriately
  • Treats all patients and co-workers with compassion, empathy, and mutual respect
  • Projects a professional manner and image
  • Consistent attendance and punctuality
  • Adherence to time clock procedures


  • Maintains confidentiality and documents accurately
  • Uses appropriate guidelines for releasing patient information
  • Practices within the scope of education, training, and personal capabilities
  • Conducts self in accordance with Suncoast s Employee Handbook.
  • Maintains awareness of federal and state health care legislation and regulations; OSHA, HIPAA, and CLIA

Physical Demands

  • Prolonged sitting/standing/walking
  • Multitasking position
  • Repetitive head, neck, hands wrists and arm motion/rotation
  • Extensive reading, writing, typing required. Typing speed 45wpm +
  • Lifting to 25lbs
  • Frequent use of office administrative, computer, and phone equipment

Qualifications and Education Requirements:

  • Medical Degree and broad-based post-graduate experience
  • Medical board certification preferred
  • A minimum of 3 or more years of experience in a clinical research position
  • Good Clinical Practice (GCP) certificate
  • Ability and willingness to travel as required
  • Excellent Communication Skills
  • Excellent presentation skills

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