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Merck Clinical Trial Manager Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

ICON

Clinical Trial Manager

Senior Clinical Trial Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

VENESCO LLC

Clinical Trial Manager

Frederick, MD · On-site

$125K - $143K/yr

Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance ...

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VENESCO, LLC

Clinical Trial Manager

Fort Detrick, MD

$125K - $143K/yr

Description Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in ...

Procter & Gamble

Clinical Trial Manager

Mason, OH · On-site

A P&G Clinical Trial Manager will be responsible for: * Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

Clinical Trial Manager Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac ...

Syneoshealth

Clinical Trial Manager

Concord, NC · On-site

Clinical Trial Manager Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug ...

Ossium Health

Clinical Trial Manager

San Francisco, CA · On-site +1

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our clinical trials and operations. In this role, you'll take ownership of the day-to-day tactical ...

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

Fortrea

Clinical Trial Manager

Durham, NC · On-site

The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to ...

Immatics NV

Clinical Trial Manager

Houston, TX

$130K - $150K/yr

We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ...

Acrivon Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$130K - $150K/yr

The Clinical Trial Manager position focuses on strategic planning, implementation, and management of a complex clinical trial. Dedicated to overseeing trials from start-up through close-out ...

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Merck Clinical Trial Manager information

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How much do merck clinical trial manager jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for merck clinical trial manager 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 some common challenges faced by Clinical Trial Managers at Merck, and how are they typically addressed?

Clinical Trial Managers at Merck often encounter challenges such as managing complex timelines, ensuring regulatory compliance across global sites, and coordinating communication between cross-functional teams. To address these, Merck provides robust project management tools, clear protocols, and ongoing training. Collaboration with regulatory, data management, and medical affairs teams is key, and regular progress meetings help keep trials on track. Flexibility and proactive problem-solving are essential skills to navigate changes or unexpected issues during the study lifecycle.

What are the key skills and qualifications needed to thrive as a Merck Clinical Trial Manager, and why are they important?

To thrive as a Merck Clinical Trial Manager, you need strong project management abilities, in-depth knowledge of clinical research regulations (such as GCP/ICH), and a relevant scientific degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and industry certifications like ACRP or SOCRA are typically required. Outstanding leadership, problem-solving, and communication skills help you coordinate teams and resolve challenges throughout the trial process. These skills and qualifications are crucial to ensuring trials are conducted efficiently, compliantly, and with high data integrity to support successful drug development.

What does a Merck Clinical Trial Manager do?

A Merck Clinical Trial Manager oversees the planning, execution, and completion of clinical trials for the company's pharmaceutical products. They coordinate cross-functional teams, ensure regulatory and compliance standards are met, manage budgets and timelines, and serve as the main point of contact between Merck and external partners or research sites. Their role is essential to ensure that clinical trials are conducted efficiently, ethically, and produce reliable data for drug development and approval.
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What cities are hiring for Merck Clinical Trial Manager jobs? Cities with the most Merck Clinical Trial Manager job openings:
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Merck Clinical Trial Manager jobs near you
Infographic showing various Merck Clinical Trial Manager 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.

Clinical Trial Manager

410 ICR United States USA

United, PA

Full-time

Posted 10 days ago

Job description

Senior Clinical Trial Manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs.

What You Will Do:

Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Key responsibilities include:

  • Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.

  • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.

  • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.

  • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.

  • Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.

  • Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • A minimum of 2+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.

  • Bachelor's degree in health, life sciences, or other relevant fields of study.

  • Preferred: previous monitoring experience

  • Experience in managing complex or global trials is advantageous.

  • Preferred: Experience in managing all trial components from start-up to database lock.

  • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.

  • Willingness to travel as required (approximately 25%)


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply