Job Responsibilities:

Responsible for the operational planning, feasibility, and execution of a clinical trial.

This may include:

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 Demonstrated ability to drive and manage operational activities on clinical protocols. This position may represent the company through external partnerships, collaborations, and key strategic engagements.

This includes the ability to:

Solid knowledge of clinical research regulatory requirements (e.g., Good Clinical Practice (GCP) and International Council for Harmonisation (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 A minimum of a Bachelor's Degree and 5+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience

OR•A Master's Degree and 3+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience•OR•

A PhD/PharmD Degree Preferred:

A Degree in life sciences Ideal candidate would have: Experienced conducting global clinical trials, including trial initiation through database lock Experienced managing and driving operational activities on protocols for immunology related clinical trials Experience with imaging vendors, clinical outcome assessments, biomarker sample collection and management, central labs and external data monitoring committee for immunology clinical trials

Highly Preferred:

Experienced conducting clinical trials for Gastroenterology, Dermatology, Rheumatology, especially autoimmune or immune-mediated disorders clinicaltrialjobs

Required Skills:

Clinical Data, Clinical Immunology, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trial Management, Clinical Trials, Ethical Standards, ICH GCP Guidelines, Project Management, Project Planning, Regulatory Compliance, Risk Management Preferred Skills:

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 salary range for this role is $117,000.00

$184,200.

00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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 https://jobs.merck.com/us/en/compensation-and-benefits . You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

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:

08/4/2026

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:

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