Principal Scientist, Stat. Programming- Eary Oncology Development (Hybrid)
We are one company, but we operate under two different corporate brand names. We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States, Canada & Puerto Rico. We are known as MSD everywhere else.
About the role
This careers website is intended for Residents of the United States, Canada & Puerto Rico. Residents in other markets, please visit our MSD Careers page. Information on this site is for the purpose of presenting career opportunities at our organization and give our audience a view of our culture, diversity and growth opportunities. Our Company is an equal opportunity employer, Minority/Female/Disability/Veteran, proudly embracing diversity in all of its manifestations.
Responsibilities
- Commence work on assigned projects
- Collaborate with cross-functional teams to achieve project goals
- Contribute to the development and maintenance of project documentation
- Ensure adherence to project timelines and deliverables
Requirements
- Bachelor's degree in relevant field
- Minimum 2 years of related work experience
- Strong communication and problem-solving skills
- Proficiency in project management tools
Qualifications
- Experience in pharmaceutical or biotech industry preferred
- Knowledge of regulatory requirements and compliance standards
- Ability to work independently and manage multiple tasks simultaneously
Skills
- Excellent written and verbal communication skills
- Strong organizational and time management skills
- Ability to work effectively in a team environment
- Basic understanding of medical terminology and drug development processes
Benefits
- Paid time off
- Health insurance
- Retirement plans
- Professional development opportunities
Pay
Compensation is commensurate with experience.
Schedule
Full-time position.
Benefits
- Paid time off
- Health insurance
- Retirement plans
- Professional development opportunities