Associate Director Study Manager (Hybrid)

Job Description The Associate Director Study Manager leads the operational planning, execution, and delivery of one or more global clinical trials. This role is accountable for ensuring high-quality study conduct, driving timelines, managing risks, and coordinating across internal and external stakeholders to meet clinical trial objectives. Key Responsibilities Lead operational planning, feasibility assessment, and execution of assigned clinical trials(s) Serve as the Clinical Trial Team (CTT) Lead and provide cross‑functional leadership Drive study strategy, operational reviews, and risk identification and mitigation planning Collaborate with internal teams, country organizations, and external partners (e.g., CROs, vendors) to deliver study objectives Oversee study timelines, key deliverables, and execution milestones Provide operational input into clinical trial documents (protocols, plans, reports) Lead governance interactions, including senior management updates and cross‑functional meetings Build team capabilities through coaching, mentoring, and development of junior staff Contribute to process improvements and serve as a subject‑matter expert Required Qualifications Education Bachelor's degree in life sciences or related field required Advanced degree preferred Experience Bachelor's with a minimum of 9 years Master's with a minimum of 6 years PhD/PharmD with a minimum of 2 years of clinical development experience Required Skills Strong knowledge of ICH/GCP and clinical research regulatory requirements Proven ability to lead global, cross‑functional clinical trial teams Strong project management, planning, and execution skills Ability to manage competing priorities and drive milestone delivery Advanced problem‑solving and risk‑management capabilities Strong stakeholder engagement and influencing skills Excellent written and verbal communication skills Proficiency in Microsoft Office tools (Excel, PowerPoint, Word) Preferred Skills Experience working in global clinical trial environments Vendor/CRO oversight experience Experience in Immunology or relevant therapeutic area Experience leading cross‑functional governance and decision‑making forums Salary & Benefits Salary range for this role is $142,400.00 – $224,100.00. We offer a comprehensive package of benefits, including medical, dental, vision, retirement benefits (401(k)), paid holidays, vacation, and compassionate and sick days. Benefits details are available at Equal Employment Opportunity 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. #J-18808-Ljbffr Merck & Co.