Senior Medical Officer Pediatrics IRB Policy

Saratoga Medical, Inc.

$170K — $200K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • MD from an accredited university
  • 10+ years of relevant experience
  • U.S. work authorization required (no visa sponsorship)
  • Pediatrics background preferred
  • Experience with IRB processes preferred
  • Strong medical writing skills preferred

Responsibilities

  • Provide medical advisory support for IRB processes and pediatric clinical care
  • Advise on clinical trial oversight and IRB processes
  • Guide pediatric clinical care and hospital pharmacy matters
  • Review clinical protocols and assess Serious Adverse Events (SAEs)
  • Serve as a safety expert on safety committees
  • Develop policies and guidelines for DMID-sponsored clinical studies

Benefits

  • Competitive rates
  • Long-term federal contract opportunities
  • Opportunities for collaboration in a clinical research environment
Full Job Description
Saratoga Medical (DBA Saratoga Ascend) is hiring Senior Medical Officer - Pediatrics, IRB & Clinical Policy for onsite opportunities in Rockville, MD. Package includes competitive rates and long-term federal contract opportunities.

Saratoga Medical (DBA Saratoga Ascend) has an exciting opportunity for a Senior Medical Officer - Pediatrics, IRB & Clinical Policy to support DMID-sponsored clinical studies in Rockville, MD. This is a great opportunity for experienced physicians seeking to provide pediatric expertise, clinical trial oversight, IRB support, and policy development in a collaborative clinical research environment.

Job Description:

  • Provide medical advisory support for IRB processes, pediatric clinical care, clinical trial oversight, and policy development.
  • Advise on IRB processes and clinical trial oversight.
  • Provide guidance on pediatric clinical care and hospital pharmacy matters.
  • Review clinical protocols and assess Serious Adverse Events (SAEs).
  • Serve as a safety expert on safety committees.
  • Develop policies and guidelines impacting DMID-sponsored clinical studies.


Required Qualifications & Documentation:

  • MD from an accredited university.
  • Minimum 10 years of relevant experience.
  • U.S. work authorization required (No visa sponsorship).
  • No security clearance required.
  • Pediatrics background with IRB experience preferred.
  • Strong medical writing skills preferred; writing samples may be requested.


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