Sr. Scientist, Clinical Operations

Job Description This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. 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. Ophthalmology/Retina related experience required. 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 Solid 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. 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 +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience. OR Master's Degree +3 years of pharmaceutical, clinical drug development, project management, and/or medical field experience. OR PhD/PharmD Degree. Degree in life sciences, preferred. Required Skills Adaptability, Biological Sciences, Clinical Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trial Management, Clinical Trials, Data Analysis, Drug Development, Ethical Standards, ICH GCP Guidelines, Identifying Risks, Life Science, Medical Writing, Motivation Management, Prioritization, Project Management, Regulatory Compliance, Regulatory Documents, Risk Monitoring, Scientific Publications, Security Risk Analysis EEOC and Equal Employment Opportunity Statement 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. Salary Range $117,000.00 - $184,200.00 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 The successful candidate will be eligible for an annual bonus and long-term incentive, if applicable. Job Details Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/A Requisition ID: R399980 Job Posting End Date: 06/1/2026 #J-18808-Ljbffr Merck & Co.