Scientist, Clinical Operations

Merck • North Wales, PA

2d • $96,200 - $151,400 • 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

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.

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
• annual bonus
• long-term incentive

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level