Study Manager, Epidemiology Operations

Job Description Support the Lead Epi Scientists by providing overall operational support for study conduct. Responsible for the coordination and execution of observational or non‑interventional research studies (including Post Authorization studies), in compliance with Good Pharmacoepidemiology Practice (GPP) and Standard Operating Procedures (SOPs). Primary Responsibilities Support operational planning and project management of epidemiology research studies Support execution, and close out of primary data collection, chart review, database, and molecular epidemiology studies in addition to other activities Provide vendor oversight including qualification efforts, confidentiality agreements, specifications, and contract reviews Liaise with the vendor and cross‑functional teams to share project status and/or needs Assist with review and finalization of all vendor documents such as the safety management, data management, communication, project management and validation plans Participate in protocol and interim/final report preparation, shepherd document through the internal review process for approval, and upload to department repository Coordination of collection, international shipment, processing by internal/external labs and data transfer for biospecimen‑based studies Participate in quality control assessments and ensure integrity of study data for reports and publications Understand, coordinate, and document adherence to internal, external, and regulatory compliance requirements Collaborate and troubleshoot issues by providing potential resolutions when necessary to ensure timely management and execution of studies Education Requirement Bachelor's degree required Master's degree (preferred) Degree in public health (or closely related discipline, such as biostatistics, epidemiology, health administration or biological sciences) Required Experience and Skills One (1) or more years of work experience within clinical/observational research or equivalent. Basic knowledge of epidemiologic or outcomes research Solid project management and prioritization skills Excellent communication and interpersonal skills and the ability to collaborate with and influence a wide variety of stakeholders Location Requirements United States and Puerto Rico residents only 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 EEO & Legal Notice 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 U.S. State Acts. Compensation & Benefits Salary range: $96,200.00 - $151,400.00. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable. We offer a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits (401(k)), paid holidays, vacation, and compassionate and sick days. #J-18808-Ljbffr Merck