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MSDPosted 1 week ago

Senior Scientist, Clinical Operations - Ophthalmology

$117,000–$184,200 year

On-siteRahway, New Jersey, United States

Full TimeSenior LevelDoctorate Or Professional DegreeEnterprise

Job Summary

Lead clinical scientist on the ophthalmology clinical trial team, driving scientific planning and execution for Phase 1-4 studies. Execute clinical protocols, collaborate with global cross-functional members including medical writers and study managers, and lead medical monitoring teams to review clinical data and protocol deviations. Participate in study setup and database design, while building team capabilities through coaching, mentoring, and performance management. Serve as a subject matter expert on process improvement teams and represent the company in external partnerships and strategic engagements. Manage direct reports, assign resources, and interpret clinical trial data to synthesize conclusions.

Required Qualifications

  • Bachelor's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
  • Master's Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
  • PhD/PharmD Degree +2 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
  • Degree in life sciences
  • Clinical Data
  • Clinical Protocol
  • Clinical Research
  • Clinical Study Design
  • Clinical Trial Compliance
  • Clinical Trials
  • Clinical Trials Analysis
  • Data Analysis
  • Drug Development
  • ICH GCP Guidelines
  • Ophthalmology
  • Regulatory Compliance
  • Strategic Thinking

Desired Qualifications

  • Master's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
  • PhD/PharmD Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
  • PhD/PharmD Degree +2 year of pharmaceutical, clinical drug development, project management, and/or medical field experience

Additional Requirements

  • US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
  • San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
  • Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

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