Scientist, Clinical Operations

MSD•Rahway, NJ

1d•Hybrid

About The Position

This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Ophthalmology/Retina related experience required.

Requirements

Working knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
Good understanding of the principles of project planning & project management
Building analytical skills to drive operational milestones
Interact with key stakeholders across department, division, and company.
Role requires a proactive approach driving toward study goals.
Problem solving, prioritization, conflict resolution, and critical thinking skills
Solid communication, writing, and presentation skills
Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
Bachelor's Degree +2 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree +1 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
Adaptability
Analytical Problem Solving
Biological Sciences
Clinical Research
Clinical Study Design
Clinical Trial Compliance
Clinical Trials
Clinical Trials Operations
Conflict Resolution
Data Management
Drug Development
Ethical Standards
Life Science
Medical Writing
Microsoft Outlook
Prioritization
Project Management
Project Planning
Regulatory Compliance
Regulatory Writing
Stakeholder Alignment
Stakeholder Relationship Management
Structured Content Management
Technical Writing
Written Communication

Nice To Haves

Ophthalmology/Retina related experience
Degree in life sciences, preferred.
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Responsibilities

May have specific operational responsibilities for a single study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities).
May be responsible for tracking study timelines using project management tools.
Shares technical expertise with team members.
May interact with internal and external stakeholders (e.g., study team, vendors, committees) in support of clinical trial objectives.