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Merck Clinical Trials Jobs (NOW HIRING)

Planning clinical trials (designing, collaborating on operational plans, etc.) based on the ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

This position contributes to the operational planning and execution of one or more clinical trials ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

This position contributes to the scientific planning and execution of one or more clinical trials ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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How much do merck clinical trials jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for merck clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Merck Clinical Trials position, and why are they important?

To thrive in a Merck Clinical Trials role, you need a background in life sciences, strong project management abilities, and experience in regulatory compliance and Good Clinical Practice (GCP) standards. Commonly used tools include clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications such as CCRA or GCP training. Excellent communication, attention to detail, and teamwork are essential soft skills for interacting with diverse stakeholders and adapting to evolving study needs. These competencies are vital for ensuring trials are conducted ethically, efficiently, and in accordance with global regulatory requirements.

What is a Merck Clinical Trials job?

A Merck Clinical Trials job involves working on the research and execution of clinical studies to evaluate the safety and effectiveness of new medications and treatments. Employees in these roles may design trials, collect and analyze data, ensure regulatory compliance, and collaborate with healthcare professionals. Positions can range from clinical research associates to data analysts and project managers. These roles are essential in bringing innovative medicines to market while upholding ethical and scientific standards.

What does a typical workday look like for someone working in Merck Clinical Trials?

A typical day in a Merck Clinical Trials position involves coordinating with cross-functional teams, monitoring study progress, ensuring adherence to protocols, and managing data collection and reporting. You'll communicate regularly with investigators, site coordinators, and regulatory bodies to address issues and keep the trial on track. Tasks may include reviewing documentation, tracking patient enrollment, and helping resolve any compliance or operational challenges. This dynamic role requires balancing multiple responsibilities in a fast-paced environment, making each day both challenging and rewarding.

More about Merck Clinical Trials jobs
What cities are hiring for Merck Clinical Trials jobs? Cities with the most Merck Clinical Trials job openings:
What are the most commonly searched types of Merck Clinical Trials jobs? The most popular types of Merck Clinical Trials jobs are:
What states have the most Merck Clinical Trials jobs? States with the most job openings for Merck Clinical Trials jobs include:
Senior Principal Scientist, Clinical Research, Immunology

Senior Principal Scientist, Clinical Research, Immunology

Merck & Co.

Rahway, NJ

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago


Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

41st of 71 rated pharmaceutical


Job description

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:- Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications.- Providing clinical development support of business development assessments of external opportunities to grow the Immunology Pipeline- Developing clinical development strategies for investigational drugs and planning clinical trials (design, operational plans, settings) based on these clinical development strategies.- Monitoring and managing the conduct of ongoing or new clinical trials for investigational drugs.- Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and- Participation in internal and joint internal/external research project teams relevant to the development of new compoundsThe Senior Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies.

Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:- Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies- Identification of scientifically and operationally strong investigators who can assist in the development of our company's investigational drugs in Immunology.- Establishing collaborative relationships with external experts in Rheumatology, Gastroenterology, Dermatology, and pulmonary disease, particularly those whose research focus and expertise can inform and assist the evaluation of the company's investigational drugs.- Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.To accomplish these goals, the Senior Director may:- Author detailed development documents, presentations, budgets, and position papers for internal and external audiences.- Facilitate collaborations with external researchers around the world.- Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.QualificationsEducation minimum required:M.D., D.O., M.D./PhD, or D.O./PhD.Required experience and skills:- Experience in the design and/or execution of phase 2 or 3 clinical trials specifically in Immunology (Rheumatology, Gastroenterology or Dermatology)- Minimum of 3 years of clinical medicine experience- Minimum of 5 years of industry experience in drug development- Demonstrated record of scientific scholarship and achievement- Strong interpersonal skills, as well as the ability to work collaboratively in a cross-functional team environment.Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, RheumatologyPreferred 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 $282,200.00 - $444,200.00This 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: RegularRelocation:DomesticVISA Sponsorship:No Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:06/11/2026 *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:R398686 Salary: . Date posted: 05/29/2026


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