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Merck Clinical Trials Jobs (NOW HIRING)

Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

... trials (design, operational plans, settings) based on these clinical development ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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 ...

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Merck Clinical Trials information

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How much do merck clinical trials jobs pay per hour?

As of Jul 28, 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:
Infographic showing various Merck Clinical Trials job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
Medical Director - Seattle Vaccine Trials Unit (VTU)

Medical Director - Seattle Vaccine Trials Unit (VTU)

Fred Hutchinson Cancer Center

Seattle, WA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago


Job description

Overview
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world's leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world's deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
The Vaccine and Infectious Disease Division (VIDD) is a recognized leader in translational and "bench-to-bedside" science. VIDD integrates the expertise and creativity of scientists in basic, translational and clinical research to prevent, treat and cure infectious diseases, including known and emerging infections of major global health importance such as influenza, SARS-CoV-2, HIV, and cancer-related infectious diseases. Applying an innovative multidisciplinary approach, VIDD houses three formal research programs that systematically pursue explicit goals aimed at eliminating the burden of death and disease from infection. These programs include Immunology and Vaccine Development; Biostatistics, Bioinformatics and Epidemiology; and Infectious Disease Sciences.
The Seattle Vaccine Trials Unit (VTU) at Fred Hutchinson Cancer Center is seeking a Medical Director to lead clinical oversight for a high-impact clinical research site focused on infectious diseases, with an emphasis on HIV vaccine development and safety.
As a part of the Vaccine & Infectious Disease Division (VIDD) and in existence since 1987, the VTU has conducted an array of studies investigating human immunology and prevention of HIV, malaria, COVID, and other viral diseases. Led by Principal Investigator Dr. Julie McElrath and co-PI Dr. Adrienne Shapiro, the VTU conducts clinical trials and observational studies. The clinical trials are mainly performed at the VTU located on First Hill. The COVID Cohort and other observational studies are based on the Fred Hutch main campus in South Lake Union.
The Medical Director will provide clinical leadership, supervise clinical staff, guide study and site operations, and partner with principal investigators and external collaborators, while fostering an inclusive and mission-driven culture.
Responsibilities
Physician Leadership & Oversight
  • Provide onsite medical oversight for all clinical trials and observational studies conducted within the VTU.
  • Ensure participant safety, protocol compliance, and adherence to Good Clinical Practice (GCP), FDA, National Institutes of Health, and institutional requirements.
  • Supervise and mentor clinical staff, including but may not be limited to clinicians (physicians, nurse practitioners, research nurses).
  • Serve as the medical authority for eligibility determinations, adverse event and reactogenicity assessment, and protocol deviation management.
  • Serve as the contact physician for research study participants and their clinical care providers.

Clinical & Study Operations
  • Partner with site leadership to ensure efficient, compliant, and high-quality clinical trial operations.
  • Oversee clinical workflows, resource allocation, and continuous performance improvement initiatives.
  • Collaborate with regulatory, pharmacy, laboratory, and data teams to ensure seamless study execution.
  • Support readiness for protocol monitoring, and audits and inspections from federal, industry sponsors, and regulatory authorities.

Scientific Collaboration & Leadership
  • Work closely with the VTU Principal Investigator, Site PIs, and collaborating clinical and research investigators to implement scientific priorities.
  • May be designated to serve as local PI on select protocols.
  • Contribute to protocol development, feasibility assessments, and study design.
  • Potential participation in leadership activities within NIH-funded research networks (e.g., HVTN), including protocol teams lead, committees, working groups and publication preparation.
  • Serve as a liaison with external partners, including academic collaborators, industry sponsors (e.g., IAVI, VIR, Janssen, Merck, Gilead), and public health stakeholders.

Program Development & Strategy
  • Help shape the strategic direction of clinical research activities.
  • Identify opportunities to expand the clinical research portfolio, including investigator-initiated studies, network, biotech and industry collaborations.
  • Support and contribute to grant applications, including NIH network funding and other sponsored research initiatives.

Culture & Community
  • Foster a clinical and research environment that values a wide range of backgrounds, perspectives, and experiences.
  • Recruit, develop, and retain high-performing clinical staff.
  • Promote a culture of collaboration, scientific rigor, and participant-centered research.
  • Work with site investigators, the VTU's community education and recruitment group, and other site staff to keep the VTU's Community Advisory Board informed of scientific progress and research directions.

Qualifications
MINIMUM QUALIFICATIONS:
  • MD or DO (or equivalent) with board certification in Infectious Diseases or a related field.
  • Active or eligible for Washington State medical licensure.
  • Demonstrated experience in clinical research and clinical trials (preferably Phase I-III).
  • Experience supervising clinical teams.
  • Deep knowledge of GCP, regulatory environments, and human subjects research.

PREFERRED QUALIFICATIONS:
  • Experience with HIV research and/or vaccine trials.
  • Prior involvement in NIH-funded clinical research networks (e.g., HVTN, DAIDS).
  • Experience serving as PI, sub-investigator, or medical monitor.
  • Track record of collaboration across academic, industry, and public sector partners.
  • Strong interest in advancing health equity and inclusive research practices.

The annual base salary range for this position is from $150,010 to $299,998, and pay offered will be based on experience and qualifications. This position may be eligible for relocation assistance.
Although Fred Hutch is not sponsoring most H-1B visas at this time, candidates who already hold an H-1B sponsored by another organization and are currently in the U.S. may be eligible for this position.
Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (22 days per year), paid sick leave (up to 30 calendar days per occurrence of a qualifying reason), paid holidays (13 days per year), and paid parental leave (up to 4 weeks).
Additional Information
We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.