Senior Study Manager, Immunology

MSD • San Diego, CA

1d • $117,000 - $184,200 • Onsite

About The Position

This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof in our Tulisokibart program. In this position, you will have the opportunity to demonstrate 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

• Demonstrated ability to drive and manage operational activities on clinical protocols.
• Solid knowledge of clinical research regulatory requirements (e.g., Good Clinical Practice (GCP) and International Council for Harmonisation (ICH))
• Ability to manage multiple competing priorities with good planning, time management and prioritization skills
• Solid understanding of the principles of project planning & project management
• Good analytical skills to drive operational milestones
• Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division
• Interact with key stakeholders across department, division, and company. Role requires a proactive approach and leadership driving toward study goals
• Applying leadership skills to processes, leading meetings, and influencing peers in a matrix environment
• Problem solving, prioritization, conflict resolution, and critical thinking skills
• Strong communication, writing, and presentation skills
• Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
• Bachelor's Degree and 5+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience -OR- Master's Degree and 3+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience -OR- PhD/PharmD Degree
• Adaptability
• Analytical Problem Solving
• Clinical Development
• Clinical Operations
• Clinical Sciences
• Conflict Management
• Critical Thinking
• Ethical Standards
• Good Clinical Practice (GCP)
• Partner Relationship Management (PRM)
• People Management
• Presentation Delivery
• Process Improvements
• Stakeholder Alignment
• Strategic Thinking

Nice To Haves

• Degree in life sciences, preferred
• Experience in conducting global clinical trials, including trial initiation through database lock
• Highly Preferred: experience in conducting clinical trials for Gastroenterology, Dermatology or Rheumatology, especially autoimmune or immune-mediated disorders
• Experience in managing and driving operational activities on protocols for immunology related clinical trials
• Leadership
• Prioritization
• Problem Solving
• Study Management

Responsibilities

• Responsible for the operational planning, feasibility, and execution of a clinical trial
• May serve as the clinical trial team lead
• May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities)
• Leads team for timeline management, risk identification and mitigation, issue resolution
• May facilitate and collaborate with key internal/external stakeholders (e.g., study team, country teams, vendors, committees) in support of clinical study objectives
• Accountable for managing any study specific partners and/or vendors

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: Senior