Study Manager - Oncology - Hybrid

MSD • Rahway, NJ

10d • 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.

Requirements

• Bachelor’s degree with two (2) years or master’s degree with one (1) year of Pharmaceutical and/or clinical drug development experience. Degree in life sciences, preferred.
• 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.)
• Adaptability
• Analytical Problem Solving
• Clinical Research
• Clinical Study Design
• Clinical Trials
• Clinical Trials Operations
• Collaborative Care
• Communication Management
• Cross-Functional Collaboration
• Data Management
• Ethical Standards
• Human Resource Management
• Interventional Oncology
• Leadership
• Management Process
• Medical Teamwork
• Medical Writing
• Oncology
• Project Management
• Regulatory Compliance
• Regulatory Writing
• Stakeholder Alignment
• Stakeholder Relationship Management

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

• We offer a comprehensive package of benefits.
• Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.
• More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits

What This Job Offers

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