MSD

Senior Scientist, Clinical Operations – ID/Vaccines

MSD

full-time

Posted on:

Location Type: Hybrid

Location: North WalesNew JerseyPennsylvaniaUnited States

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Salary

💰 $117,000 - $184,200 per year

Job Level

About the role

  • This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.
  • Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s).
  • Serving as the lead clinical scientist on the clinical trial team.
  • Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director.
  • Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments);
  • Partners with the Study Manager on study deliverables.
  • Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming.
  • Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct.
  • Providing tactical/scientific mentorship to other clinical scientists.

Requirements

  • Bachelor's degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR master's degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience OR PhD/PharmD degree
  • Degree in life sciences, preferred.
  • Accountability
  • Adaptability
  • Clinical Data
  • Clinical Study Design
  • Clinical Trial Compliance
  • Clinical Trial Management
  • Data Analysis
  • Ethical Standards
  • ICH GCP Guidelines
  • Medical Writing
  • Motivation Management
  • Regulatory Documents
Benefits
  • medical
  • dental
  • vision healthcare and other insurance benefits (for employee and family)
  • retirement benefits, including 401(k)
  • paid holidays
  • vacation
  • compassionate and sick days
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trial managementclinical study designdata analysismedical writingclinical dataregulatory documentsICH GCP guidelinesprotocol developmentCRF designproject management
Soft Skills
accountabilityadaptabilitymotivation managementtactical mentorshipcollaborationleadershipcommunicationinterpersonal skillsproblem-solvingteamwork