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Clinical Research Physician/Investigator

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

View more

Specialty
Dermatology
Hours
Full Time
Position Type
Permanent

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

Role and Responsibilities

Administrative

  • 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

Professional

  • 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

Communication

  • 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

Legal

  • 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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