Study Manager - Oncology - Hybrid

Merck Sharp & Dohme Corp

Multiple Locations, US
Base: $96,200.00 - $151,400.00; bonus/equity: annu...
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Bachelor's degree with 2 years experience
Knowledge of gcp and ich regulatory requirements
Project management and timeline tracking skills
** Merck Sharp & Dohme Corp is seeking a Study Manager for Oncology, primarily focused on the operational planning and execution of clinical trials. The role requires project management skills, knowledge of clinical research regulations, and effective communication, and offers a hybrid work option. **

Job Summary

  • This position contributes to the operational planning and execution of one or more clinical trials within a global cross-functional team.
  • The role involves managing study timelines, tracking supplies, and interacting with internal and external stakeholders to support clinical trial objectives.
  • Candidates are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

Match Score: 75

** Merck Sharp & Dohme Corp is seeking a Study Manager for Oncology, primarily focused on the operational planning and execution of clinical trials. The role requires project management skills, knowledge of clinical research regulations, and effective communication, and offers a hybrid work option. **

Salary

Base: $96,200.00 - $151,400.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • Bachelor's degree with 2 years experience
  • Knowledge of GCP and ICH regulatory requirements
  • Project management and timeline tracking skills
  • Experience in pharmaceutical or clinical drug development
  • Intermediate Microsoft Office proficiency

Nice-to-have

  • Master's degree preferred
  • Life sciences degree background
  • Proactive problem-solving approach
  • Cross-functional collaboration experience
  • Oncology domain knowledge

Key Requirements

  • Bachelor's degree required (or Master's with 1 year exp)
  • 2 years Pharmaceutical/Clinical Drug Development experience
  • Working knowledge of GCP and ICH regulations

Work Rights

Not specified

Tailored Resume

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