Scientist, Clinical Operations

Job Description This position contributes to the operational planning and execution of one or more clinical trials. In this role you will develop leadership and technical skills as part of a global, cross‑functional team, applying project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for a single study or across multiple studies, including 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. Core Skills 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; 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.). Education and Experience 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. Degree in life sciences, preferred. Required Skills 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. 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. If you need an accommodation during the application or hiring process, please let us know. Location Restrictions 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. Salary and Benefits Salary Range: $96,200.00 – $151,400.00. This range is the lowest to highest salary we in good faith believe we would pay for this role at the time of posting. Eligibility for annual bonus and long‑term incentive, if applicable. Comprehensive benefits include medical, dental, vision, retirement (401(k)), paid holidays, vacation, and compassionate and sick days. Equal Employment Opportunity As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants 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 affirmative action requirements for protected veterans and individuals with disabilities. More information about personal rights under U.S. EEO laws is available through EEOC resources. Job Details Requisition ID: R399978 Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/A #J-18808-Ljbffr Merck