Ensure GxP compliance in data science programming for clinical trials. * Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency. Executive Communication:
Ensure GxP compliance in data science programming for clinical trials. * Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency. Executive Communication:
Associate Director, Clinical Development Trial Lead (CDTL)
Indianapolis, IN · On-site
$32 - $43.75/hr
... clinical trials. This highly visible leadership role offers the opportunity to oversee study ... Demonstrate independent leadership and influence when working with study teams, management, and ...
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Associate Director, Clinical Development Trial Lead (CDTL)
Indianapolis, IN · On-site
$32 - $43.75/hr
... clinical trials. This highly visible leadership role offers the opportunity to oversee study ... Demonstrate independent leadership and influence when working with study teams, management, and ...
Lead global/regional clinical trials from start-up through close-out. * Develop and execute study management plans aligned with contract and strategy. * Manage timelines, budgets, and risk mitigation ...
New
Lead global/regional clinical trials from start-up through close-out. * Develop and execute study management plans aligned with contract and strategy. * Manage timelines, budgets, and risk mitigation ...
New
Clinical Project Manager, Internal Medicine, IQVIA Biotech
Indianapolis, IN · On-site
$93K - $232K/yr
Lead global/regional clinical trials from start-up through close-out. * Develop and execute study management plans aligned with contract and strategy. * Manage timelines, budgets, and risk mitigation ...
New
Clinical Project Manager, Internal Medicine, IQVIA Biotech
Indianapolis, IN · On-site
$93K - $232K/yr
Lead global/regional clinical trials from start-up through close-out. * Develop and execute study management plans aligned with contract and strategy. * Manage timelines, budgets, and risk mitigation ...
New
As Director/General Manager, you will lead operations and contribute to growth at our clinical trial packaging facility. This leadership role carries full P&L responsibility and accountability for ...
As Director/General Manager, you will lead operations and contribute to growth at our clinical trial packaging facility. This leadership role carries full P&L responsibility and accountability for ...
As Director/General Manager, you will lead operations and contribute to growth at our clinical trial packaging facility. This leadership role carries full P&L responsibility and accountability for ...
As Director/General Manager, you will lead operations and contribute to growth at our clinical trial packaging facility. This leadership role carries full P&L responsibility and accountability for ...
Associate Director, Clinical Development Trial Lea
Indianapolis, IN · On-site
$217K/yr
Remote options will be considered Highly Desired Skills: • Experience with oncology (early & late phase clinical trials) • Applied knowledge of project management methodology, processes and tools ...
Associate Director, Clinical Development Trial Lea
Indianapolis, IN · On-site
$217K/yr
Remote options will be considered Highly Desired Skills: • Experience with oncology (early & late phase clinical trials) • Applied knowledge of project management methodology, processes and tools ...
Clinical Data Coordinator (Clinical Research Technician)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists in the conduct of clinical research studies or trials following established protocols and ... Maintains and manages inventory and research study supplies; may be responsible for facilitating ...
Clinical Data Coordinator (Clinical Research Technician)
Indianapolis, IN · On-site
$23.25 - $30.75/hr
Assists in the conduct of clinical research studies or trials following established protocols and ... Maintains and manages inventory and research study supplies; may be responsible for facilitating ...
Use project management skills, processes, and tools to develop and execute local, regional, and/or global clinical trials. * Understand the scope of work required to complete the clinical trial ...
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Use project management skills, processes, and tools to develop and execute local, regional, and/or global clinical trials. * Understand the scope of work required to complete the clinical trial ...
Support or lead patient recruitment, retention, and engagement strategies across clinical trials ... Manage complex project timelines, dependencies, deliverables, approvals, and risks. * Coordinate or ...
New
Support or lead patient recruitment, retention, and engagement strategies across clinical trials ... Manage complex project timelines, dependencies, deliverables, approvals, and risks. * Coordinate or ...
New
Imaging Specialist Manager
Indianapolis, IN · On-site +1
IMAGING SPECIALIST MANAGER LIVE What you will do In this vital role you will plan and execute imaging operations for clinical trials globally. You will manage and coordinate the operational imaging ...
Imaging Specialist Manager
Indianapolis, IN · On-site +1
IMAGING SPECIALIST MANAGER LIVE What you will do In this vital role you will plan and execute imaging operations for clinical trials globally. You will manage and coordinate the operational imaging ...
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS). 5. ...
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS). 5. ...
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS). 5. ...
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS). 5. ...
... and management of projects within late phase clinical trials areas. Focused therapeutic areas : Metabolic, Hepatology, Cardiovascular & Respiratory Key Responsibilities: Strategic Planning:
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... and management of projects within late phase clinical trials areas. Focused therapeutic areas : Metabolic, Hepatology, Cardiovascular & Respiratory Key Responsibilities: Strategic Planning:
... and management of projects within late phase clinical trials areas. Focused therapeutic areas : Metabolic, Hepatology, Cardiovascular & Respiratory Key Responsibilities: Strategic Planning:
Quick apply
... and management of projects within late phase clinical trials areas. Focused therapeutic areas : Metabolic, Hepatology, Cardiovascular & Respiratory Key Responsibilities: Strategic Planning:
Clinical Research Physician - Medical Development - Diabetes
Indianapolis, IN · On-site
$198 - $356.40/hr
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS)
Clinical Research Physician - Medical Development - Diabetes
Indianapolis, IN · On-site
$198 - $356.40/hr
... global clinical trials in support of registration and commercialization of the product; the ... Participate in risk management planning along with affiliates and Global Patient Safety (GPS)
Oncology RN - Clinical Research
Indianapolis, IN · On-site
$40 - $45/hr
Registered Nurse - Oncology (Phase I Trials) *Clinical research experience NOT required* This ... Strong organizational and time management skills to handle patient visits ranging from 1 to 8 hours.
Quick apply
Oncology RN - Clinical Research
Indianapolis, IN · On-site
$40 - $45/hr
Registered Nurse - Oncology (Phase I Trials) *Clinical research experience NOT required* This ... Strong organizational and time management skills to handle patient visits ranging from 1 to 8 hours.
The Manager, Clinical Development Trial Lead (CDTL) leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to ...
The Manager, Clinical Development Trial Lead (CDTL) leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to ...
The Manager, Clinical Development Trial Lead (CDTL) leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to ...
The Manager, Clinical Development Trial Lead (CDTL) leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to ...
Clinical Research Coordinator II
$22.50 - $29.75/hr
Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision * Manage complex study visit schedules and protocol-related ...
Clinical Research Coordinator II
$22.50 - $29.75/hr
Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision * Manage complex study visit schedules and protocol-related ...
Clinical Trials Manager information
See Indiana salary details
$27.45 - $33.27
4% of jobs
$33.27 - $39.09
6% of jobs
$39.09 - $44.92
7% of jobs
$49.28 is the 25th percentile. Wages below this are outliers.
$44.92 - $50.74
9% of jobs
$50.74 - $56.56
15% of jobs
The median wage is $59.13 / hr.
$56.56 - $62.38
18% of jobs
$66.53 is the 75th percentile. Wages above this are outliers.
$62.38 - $68.21
21% of jobs
$68.21 - $74.03
7% of jobs
$74.03 - $79.85
6% of jobs
$79.85 - $85.67
3% of jobs
$85.67 - $91.50
2% of jobs
$27
$59
$91
How much do clinical trials manager jobs pay per hour?
What does a clinical trials manager do?
What are some common challenges faced by clinical trials managers and how can they be addressed?
What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?
What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?
| Aspect | Clinical Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees entire clinical trial process, manages teams, ensures compliance, and handles budgets. | Assists with patient recruitment, data collection, and site coordination under supervision. |
| Required Credentials | Bachelor’s or higher in life sciences, often with project management experience. | Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred. |
| Work Environment | Works in clinical trial sites, research organizations, or pharmaceutical companies. | Primarily works at clinical sites, hospitals, or research facilities. |
In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.
What are the most commonly searched types of Clinical Trials jobs in Indiana?
The most popular types of Clinical Trials jobs in Indiana are:
What are popular job titles related to Clinical Trials Manager jobs in Indiana?
For Clinical Trials Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Trials Manager jobs in Indiana look for?
The top searched job categories for Clinical Trials Manager jobs in Indiana are:
- Clinical Trial Recruitment Specialist
- Clinical Study Manager
- Remote Merck Clinical Trials
- Sr Clinical Data Manager
- Senior Clinical Data Standards
- Clinical Trials Assistant
- Clinical Research Program Manager
- Merck Clinical Trial Manager
- Clinical Research Associate Manager
- Contract Senior Clinical Research Associate
What cities in Indiana are hiring for Clinical Trials Manager jobs?
Cities in Indiana with the most Clinical Trials Manager job openings:

Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Job description
At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.
We are seeking a visionary leader to shape and drive Clinical Data Science strategy across our global clinical development portfolio. This role ensures the rigorous application of statistical principles and advanced data science methodologies to optimize clinical trial efficiency and accelerate innovation. The Executive Director will spearhead the integration of AI/ML solutions for applications in disease diagnosis, modeling, imaging, genomics, proteomics, and precision medicine. Acting as the primary data science representative to global regulatory authorities, this individual will defend strategies and influence industry standards.
Strategic Leadership:
- Define and execute Clinical Data Science strategies for clinical studies and development plans across the portfolio.
- Serve as the primary spokesperson for Data Science at Health Authority meetings, leading preparation of responses and influencing regulatory perspectives.
Innovation & Execution:
- Drive adoption of cutting-edge AI/ML methodologies for disease modeling, biomarker analysis, and precision medicine.
- Oversee multiple large-scale, critical data science initiatives, ensuring timely, high-quality deliverables aligned with industry best practices.
Risk Management & Problem Solving:
- Evaluate analytical options, proactively identify risks, and develop novel solutions to complex challenges.
Thought Leadership & External Engagement:
- Represent the organization at technical seminars and conferences; build networks with industry experts to advance best practices.
Team Leadership & Development:
- Manage and mentor a diverse team of data scientists and people managers across geographies.
- Foster career growth through open dialogue, performance management, and strategic development planning.
Operational Excellence:
- Ensure GxP compliance in data science programming for clinical trials.
- Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency.
Executive Communication:
- Deliver clear, compelling communication of complex data science concepts to internal and external stakeholders with executive presence.
Qualifications
- Ph.D. in Biostatistics or a Master's Degree in Biostatistics in combination with a Ph.D.in Bioinformatics or related computational sciences.
- Deep expertise in statistical methods and their application in clinical trials.
- Minimum 10 years of industry experience in clinical development, including Data Science and Biostatistics.
- Recognized thought leader in at least one data science discipline (e.g., AI/ML modeling, precision medicine).
- Proven experience presenting at external forums and influencing regulatory authorities.
- Strong people leadership experience in a Data Science setting.
- Prior research experience in neurology, particularly Alzheimer's disease biomarkers (plasma, CSF, imaging), strongly preferred.
Eisai Salary Transparency Language:
The annual base salary range for the Executive Director, Clinical Data Science is from :$273,200-$358,600Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.
Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.
Certain other benefits may be available for this position, please discuss any questions with your recruiter.
Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.
Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:
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E-Verify Participation
About Eisai
Sourced by ZipRecruiter
Eisai is a global pharmaceutical company (headquartered in Woodcliff Lake, NJ, US), renowned for its innovative research and development in neuroscience and oncology. The primary focus of the company is to provide therapeutic treatments and solutions for diseases like Alzheimer's, cancer, and other neurological disorders. Eisai was founded in Japan in 1941 and has since developed a strong presence across international markets. Eisai's core values center around their philosophy of 'human health care' (hhc), where they aim to make significant and positive contributions to patients and their families' healthcare worldwide.
Industry
Pharmaceutical and medicine manufacturing and biotechnology research and development
Company size
1,001 - 5,000 Employees
Headquarters location
Nutley, NJ, US