Associate Director, Study Manager - Atherosclerosis and Metabolism
$142.4k - $224.1kFull-time
Merck & Co.
Job Description This position participates in the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your advanced leadership and technical skills as part of a global, cross-functional team. You will build and coach your team in the development of project management, communication, and collaboration skills in support of our clinical trials. - Job Responsibilities
Adaptability, Analytical Problem Solving, Clinical Data Management, Clinical Study Management, Collaboration, Detail-Oriented, Ethical Standards, Good Clinical Practice (GCP), Problem Solving, Stakeholder Alignment, Strategic Thinking Preferred Skills:
Process Improvements, Program Management, Project Management Current Employees apply HERE Current Contingent Workers apply HERE 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. Please click here if you need an accommodation during the application or hiring process. 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• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is:
USA - New Jersey - Rahway Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is:
$142,400.00 - $224,100.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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. 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 . Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. Additional location(s) Compensation Information: 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 Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- 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:
10/24/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R421910
- Responsible for the operational planning, feasibility, execution and conduct of clinical trial(s).
- Serves as the Clinical Trial Team (CTT) lead
- Leads and directs teams in key study planning, development, and execution elements (e.g. operational reviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross functional meetings and governance).
- Responsible for facilitating and collaborating with key internal/external stakeholders (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.
- Liaises with partners, vendors, and vendor management team.
- Review and provide clinical operations input into relevant clinical documents such as the protocol and other documents as appropriate.
- May serve as a subject matter expert and/or participate on process improvement teams.
- Builds talent and capabilities of junior team members through proactive coaching, mentoring and development opportunities.
- May include management of direct/indirect reports including assignment of resources, professional development, and performance management.
- Strong knowledge of clinical research regulatory requirements e.g., Good Clinical Practice (GCP) and International Council for Harmonisation (ICH)
- Proven ability to manage competing priorities and effectively delegate and assign activities to meet the business needs
- Ability to develop short and mid-range project plans that are realistic and effective at meeting goals
- Strong 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, strategic thinking and leadership driving toward study goals.
- Demonstrated leadership skills in programs & processes, leading meetings and influencing peers and direct/indirect reports in a matrix environment.
- Problem solving, prioritization, conflict resolution, and critical thinking skills
- Strong communication, writing, and presentation skills
- Proficient knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
- Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience
- -OR- Master's Degree and 6+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience
- -OR- PhD/PharmD Degree and 2+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience
- Degree in life sciences, preferred
Adaptability, Analytical Problem Solving, Clinical Data Management, Clinical Study Management, Collaboration, Detail-Oriented, Ethical Standards, Good Clinical Practice (GCP), Problem Solving, Stakeholder Alignment, Strategic Thinking Preferred Skills:
Process Improvements, Program Management, Project Management Current Employees apply HERE Current Contingent Workers apply HERE 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. Please click here if you need an accommodation during the application or hiring process. 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• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is:
USA - New Jersey - Rahway Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is:
$142,400.00 - $224,100.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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. 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 . Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. Additional location(s) Compensation Information: 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 Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- 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:
10/24/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R421910
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Associate Director, Study Manager - Atherosclerosis and Metabolism in Rahway, NJ vacancy
$142.4k - $224.1k
...Associate Director role leading operational planning and execution of clinical trials in metabolic disease. Reports to senior management while building and coaching teams across global, cross-functional... ...Trial Team lead Direct key study planning and development...SuggestedWork at office$142.4k - $224.1k
...Associate Director overseeing operational planning and execution of clinical trials in metabolic disease areas. This role leads cross-functional teams, manages study conduct and regulatory compliance, and develops junior staff while collaborating with internal and external...SuggestedWork at office$129k - $203.1k
...generates audit reports, communicates results to the relevant QA management and external relevant stakeholders (e.g. Clinical Operations),... ...cultural considerations, responsibilities for work in global studies and local regulations in the China related to GCP and new drug...SuggestedFull timeFor contractorsLocal areaFlexible hours$142.4k - $224.1k
Job DescriptionThe Associate Director, Project Management, within Metrics, Analytics & Performance (MAP) will lead project management related to the... ...execution, and monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (...SuggestedFull timeFor contractorsLocal areaFlexible hours- ...audits and collaborate on quality improvements that support global studies.Compensation / Benefitsmedical, dental, vision... ...partners; produce audit reports and communicate findings to QA management and stakeholders; drive corrective and preventative actions to...SuggestedLocal area
$129k - $203.1k
...generates audit reports, communicates results to the relevant QA management and external relevant stakeholders (e.g. Clinical Operations),... ...cultural considerations, responsibilities for work in global studies and local regulations in the China related to GCP and new drug...Full timeFor contractorsLocal areaFlexible hours$142.4k - $224.1k
...Associate Director role leading operational planning and execution of clinical trials within an... ...directs cross-functional teams through study development and execution phases while... ...professional development, and performance management Provide clinical operations input on...Work at office- Associate Director, Study Integration Manager (M-track) Leads a team responsible for delivering trial-level technical data management components (eCRFs, integrations, validation, reports) ensuring quality, compliance, and audit readiness within clinical trials. Objectives...
$142.4k - $224.1k
...inhalation, implantation, and injection.The Associate Principal Scientist will provide end‑to‑... ..., including design controls, risk management, manufacturing process development and validation... ...of accelerated and real time aging studies including bridging studies at the device...Full timeFor contractorsLocal areaWorldwideFlexible hours$156.9k - $247k
...from business development to late lifecycle management. As we endeavor, we are seeking a dynamic talent for the role of Associate Director, Primary Market Research . Position... ...techniques to design effective research studies. Evaluate and apply innovative market...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$129k - $203.1k
Job DescriptionThe Associate Director, Quality Assurance will be responsible for quality leadership and subject matter expertise in Quality Operations... ...regulatory standards.Essential Duties and Responsibilities:Manage projects and tasks affiliated with Quality oversight of GMP...Full timeFor contractorsLocal areaFlexible hours- ...Merck seeks an Associate Principal Scientist to lead design verification strategies for drug... ...Direct accelerated and real-time aging studies at component and combination product... ...development experience Leadership experience managing design verification programs and cross-...
$142.4k - $224.1k
Job DescriptionThe Global Clinical Supply (GCS) organization is responsible for managing the end-to-end integrated clinical supply chain across the Company’s Research Laboratories portfolio of clinical trials. GCS oversees the sourcing, labeling, packaging, and global...Full timeContract workFor contractorsLocal areaWorldwideFlexible hoursShift work$156.9k - $247k
...Responsibilities Reporting to the Executive Director, Integrated Business Operations & Launch Excellence, the Associate Director, Global Oncology Marketing is... ...mitigate risks as appropriate Support knowledge management and best practice sharing across the...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$156.9k - $247k
...Associate Director role leading launch planning for two to three priority oncology products within a five-year pipeline. Responsible for ensuring... ...pharmaceutical industry experience Demonstrated project management and launch planning expertise Strong commercial acumen...$142.4k - $224.1k
...innovative medicines that help people around the globe. The Associate Director, US Ophthalmology Payer Marketing , is responsible for... ...across functions-including Brand Marketing, Field Reimbursement Managers (FRMs), Integrated Account Management, Outcomes Research /...Permanent employmentFull timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work$54.81 per hour
...Join to apply for the Study Manager role at Vita Global Sciences, a Kelly Company . Base pay range $54.81/hr - $54.81/hr Kelly Science and Clinical FSP is currently seeking a Study Manager for a long‑term engagement with one of our Global Pharmaceutical clients. This person...Full timeContract workWork at office$142.4k - $224.1k
...campaign and channel performance into business-relevant narratives and recommendations that inform future business decisions.6. Risk Management & Feedback Loop Proactively flag capacity constraints, conflicting priorities, or scope changes before they become delivery risks...Full timeFor contractorsLocal areaFlexible hoursShift workAfternoon shift3 days per week$173.2k - $272.6k
...Job DescriptionRole Summary:The Global Associate Director Medical Affairs (GADMA) has scientific... ...the competitive intelligence (CI) team.Manages programs (patient support, educational... ...stewardshipParticipates in Investigator-Initiated Study proposals reviews in collaboration and...For contractorsLocal areaFlexible hours$142.4k - $224.1k
...Description The Global Commercial Metabolism Team is responsible for shaping the global... ...customers, and the enterprise. The Associate Director, Global Marketing - Obesity will... ...Executional Excellence: Ability to manage multiple priorities, clarify decisions...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$117k - $184.2k
...Senior Study Manager position leading operational planning and execution of clinical trials within the immunology program. The role oversees feasibility assessments, protocol execution, cross-functional team coordination, and stakeholder engagement across global clinical...$100k - $110k
...gender identity, national origin, medical condition, disability, veterans status, or any other basis protected by law. Associate Director, Project Management - WebMD/Medscape Medical AffairsAre you a seasoned digital project manager or former account director from a med...Worldwide- Merck seeks an Associate Director, US Marketing Engagement - HIV Prep, to translate complex data into actionable insights shaping brand strategy, launch readiness, and performance measurement. You will partner with US HIV Prep Marketing to frame questions, prioritize analytics...
$221.41k - $280.07k
...Alliance Sales Executive, Associate Director: Microsoft – State & Local Government At EY, we're all in to shape your future with confidence... ...net-new business hunter, not solely an account or alliance manager ~ Direct experience selling to State and Local Government...Summer holidayLocal areaFlexible hours- A pharmaceutical company is seeking an Associate Director, Site Services Procurement Category Lead. The ideal candidate will have a bachelor... ...include developing category strategies, leading teams, and managing suppliers. The role operates within a hybrid work model, requiring...3 days per week
- ...Associate Director position in Quantitative Pharmacology and Pharmacometrics within a major biopharmaceutical company's cardiometabolic research... ...approaches for regulatory decision-making Contribute to study design, protocol development, data interpretation, and...
$156.9k - $247k
...Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical... ...new drugs/INDs, clinical study reports (CSRs), clinical trial applications... ...Pharmacometrics, Stakeholder Relationship Management Preferred Skills: NONMEM, Oncology...Full timeFor contractorsLocal areaRemote workWorldwideRelocationVisa sponsorshipFlexible hoursShift work$156.9k - $247k
...collaborative, and scientifically driven Associate Director to help support our growing... .... Collaborate across disciplines on study design, protocol development, study execution... ...PKPD Modeling, Stakeholder Relationship Management Preferred Skills: Current Employees...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$156.9k - $247k
...from business development to late lifecycle management. As we endeavor, we are seeking a dynamic talent for the role of Associate Director, Primary Market Research . Position... ...techniques to design effective research studies. Evaluate and apply innovative market...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$142.4k - $224.1k
...scientific planning, strategy, and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will... ...global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.Job Responsibilities...Full timeFor contractorsLocal areaFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Study Manager - Atherosclerosis and Metabolism. Be the first to apply!
Related searches
- associate director clinical data management Rahway, NJ
- associate director marketing Rahway, NJ
- remote associate product manager Rahway, NJ
- associate manager Rahway, NJ
- associate director market research Rahway, NJ
- associate director clinical research Rahway, NJ
- associate director Rahway, NJ
- associate marketing manager Rahway, NJ
- associate scientific director Rahway, NJ
- associate product manager web Rahway, NJ



