Senior Clinical Scientist
MSD
full-time
Posted on:
Location Type: Hybrid
Location: North Wales • California, New Jersey, Pennsylvania • 🇺🇸 United States
Visit company websiteSalary
💰 $114,700 - $180,500 per year
Job Level
Senior
Tech Stack
Google Cloud Platform
About the role
- 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)
- Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming
- 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
- Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
- Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
- Experience in conducting global clinical trials, including trial initiation through database lock
- Experience in conducting clinical trials in ophthalmology, such as uveitis, AMD (age-related macular degeneration), thyroid eye disease
- Experience in developing protocols and study related documents for ophthalmology clinical trials
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
clinical protocol executionmedical monitoringdata interpretationCRF designclinical trial data analysisprotocol developmentstudy document developmentproject managementclinical research regulatory knowledgeophthalmology clinical trials
Soft skills
leadershipcollaborationmentorshipanalytical skillscommunication
Certifications
Bachelor's DegreeMaster's DegreePhDPharmD