Clinical Study Manager

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.- Job 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 Core Skills Demonstrated ability to drive and manage operational activities on clinical protocols. This position may represent the company through external partnerships, collaborations, and key strategic engagements. This includes the ability to: 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.) Education/Experience 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 Degree in life sciences, preferred Ideal candidate would have: 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 Required Skills: 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 Preferred Skills: Leadership Prioritization Problem Solving Study Management US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement Learn more about your rights, including under California, Colorado and other US State Acts San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. 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 . Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Not Applicable Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/A Job Posting End Date: 09/24/2026 Requisition ID: R415525 #J-18808-Ljbffr