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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 Sep 4, 2026, the average hourly pay for merck clinical trial manager in Indiana is $59.49, according to ZipRecruiter salary data. Most workers in this role earn between $48.27 and $67.02 per hour, depending on experience, location, and employer.

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.

What are the key skills and qualifications needed to thrive as a Merck clinical trial manager?

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 are some common challenges faced by Merck clinical trial managers, 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.

How much do Merck clinical trial managers make?

Merck clinical trial managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and level of responsibility. Salaries can vary based on factors such as certifications, education, and the complexity of trials managed.

How much does a Merck Clinical Trial Manager earn?

A Merck Clinical Trial Manager typically earns between $90,000 and $130,000 annually, depending on experience, location, and education. They often oversee clinical trial operations, requiring knowledge of regulatory requirements and project management skills.

What are popular job titles related to Merck Clinical Trial Manager jobs in Indiana?

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What job categories do people searching Merck Clinical Trial Manager jobs in Indiana look for?

The top searched job categories for Merck Clinical Trial Manager jobs in Indiana are:

What cities in Indiana are hiring for Merck Clinical Trial Manager jobs?

Cities in Indiana with the most Merck Clinical Trial Manager job openings:

Merck Clinical Trial Manager jobs near you

Senior Clinical Trial Manager, Veterinary Medicine

Elanco Animal Health Incorporated

Indianapolis, IN • On-site

Full-time

Retirement, PTO

Posted 13 days ago

Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Job Description
Your Role: Clinical Trial Manager, Veterinary Medicine
This position will function in the efficient and effective management and execution of clinical studies. The individual will be responsible for continuing to grow and develop capabilities in clinical trial implementation. The incumbent will coordinate, oversee, and monitor clinical studies needed for the registration of global products for Elanco. The individual will maintain an excellent working knowledge of government regulations and policies pertaining to clinical trials, VICH-GCP guidelines, company Standard Operating Procedures (SOPs), and assigned study protocols. The position will interact with US research scientists and the global research and development teams to gain regulatory approval of these products.
Your Responsibilities:
  • Plan, manage, and oversee all phases of veterinary clinical trials, including study initiation, site recruitment and training, monitoring, execution, close-out, and compliance with study protocols and SOPs.
  • Support high-quality study delivery through protocol and final report review, data capture design, QA/audit responses, risk management, and continuous improvement of trial conduct and data quality.
  • Partner cross-functionally with R&D, commercial teams, external partners, and clinical sites to ensure alignment, timelines, quality, and successful study execution.
  • Support regulatory and operational activities, including FDA/USDA inspections, communication with regulators, budgeting, contracting, invoicing, forecasting, and vendor selection and oversight.
  • Provide leadership and mentorship to study monitors and administrators while contributing to a high-performing, innovative team culture aligned with Elanco values.

Minimum Qualification (education, experience and/or training, required certifications)
  • Education: Bachelor's degree in a science or health related field and 5+ years' experience in veterinary clinical trial management and execution of clinical studies
  • Required Experience: Strong background in monitoring of veterinary clinical studies. Working knowledge of computer applications including electronic data capture system(s), MS Word, Outlook, Teams, Excel, PowerPoint, Adobe, and SMF applications
  • Required veterinary experience: Candidates must have direct experience managing and executing veterinary clinical trials. Experience limited to human clinical trials, general clinical operations, or adjacent regulatory/project management work will not meet this requirement.
  • Top 2 skills: Previous trial management experience in veterinary medicine. Proven ability to manage cross-functional teams and collaborate with internal and external stakeholders, including regulatory bodies (FDA/USDA).

What Will Give You a Competitive Edge (Preferred Qualifications):
  • Has experience supporting FDA and USDA inspections and audits, ensuring trial compliance with GCP and regulatory requirements.
  • Has led cross-functional collaborations with R&D, commercial teams, and external partners to drive end-to-end clinical trial execution, including protocol development, budgeting, vendor oversight, and study management.

Additional Information:
  • Location: Indianapolis, IN - Hybrid
  • Travel: Minimal 25%

Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
  • Multiple relocation packages
  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Flexible work arrangements
  • Up to 6% 401K matching

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
#LI-RH1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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