As clinical trials manager, responsibilities include review and mastery of clinical research documents (protocols, case report forms, reports and statistical analysis), monitoring recruitment and ...
As clinical trials manager, responsibilities include review and mastery of clinical research documents (protocols, case report forms, reports and statistical analysis), monitoring recruitment and ...
Clinical Trials Manager
Washington, DC · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research documents (protocols, case report forms, reports and statistical analysis), monitoring recruitment and ...
Clinical Trials Manager
Washington, DC · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research documents (protocols, case report forms, reports and statistical analysis), monitoring recruitment and ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Chicago, IL · On-site +1
Job Summary The Clinical Trials Manager will manage and coordinate a variety of complex and independent activities involved with planning and conducting multiple research studies for the Alliance.
Clinical Trials Manager
Chicago, IL · On-site +1
Job Summary The Clinical Trials Manager will manage and coordinate a variety of complex and independent activities involved with planning and conducting multiple research studies for the Alliance.
As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial ...
As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial ...
Clinical Trials Manager
Chicago, IL · On-site
Job Summary The Clinical Trials Manager will manage and coordinate a variety of complex and independent activities involved with planning and conducting multiple research studies for the Alliance.
Clinical Trials Manager
Chicago, IL · On-site
Job Summary The Clinical Trials Manager will manage and coordinate a variety of complex and independent activities involved with planning and conducting multiple research studies for the Alliance.
As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial ...
As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial ...
Clinical Trials Manager
Marlborough, MA · On-site
Our account managers and recruiters have over a decade of experience in various verticals. GCM ... Working in a GxP environment. experience with clinical outsourcing, clinical trials required for ...
Clinical Trials Manager
Marlborough, MA · On-site
Our account managers and recruiters have over a decade of experience in various verticals. GCM ... Working in a GxP environment. experience with clinical outsourcing, clinical trials required for ...
Clinical Trials Manager
Boston, MA · On-site
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
Clinical Trials Manager
Boston, MA · On-site
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
Clinical Trials Manager
Foster City, CA · On-site
In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
Clinical Trials Manager
Foster City, CA · On-site
In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
Clinical Trials Manager
Shreveport, LA · On-site
Clinical Trials Manager Lead the team that runs our clinical research Location: Shreveport, LA (standard medical office; some local travel) Type: Full-time · Exempt · Reports to Principal/President ...
New
Quick apply
Clinical Trials Manager
Shreveport, LA · On-site
Clinical Trials Manager Lead the team that runs our clinical research Location: Shreveport, LA (standard medical office; some local travel) Type: Full-time · Exempt · Reports to Principal/President ...
New
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ... Manages a geographical (region)s of assigned clinical studies, multiple components of larger ...
The Manager Clinical Trials position monitors progress and performance of all projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other ...
The Manager Clinical Trials position monitors progress and performance of all projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other ...
Supports the planning, execution and reporting of clinical programs/ trials Clinical Research Protocols Reviews Clinical Protocols Study Management Reviews study documents (i.e., investigator ...
Supports the planning, execution and reporting of clinical programs/ trials Clinical Research Protocols Reviews Clinical Protocols Study Management Reviews study documents (i.e., investigator ...
Clinical Trials Manager - Oncore Data
Oklahoma City, OK · On-site
$55K - $72K/yr
Clinical Trials Manager - Oncore Data Job no: 493887 Work type: Managerial Location: Oklahoma City Categories: Technology/Research Pay Range: Targeted salary from $55,800 - $72,600 annually, based on ...
Clinical Trials Manager - Oncore Data
Oklahoma City, OK · On-site
$55K - $72K/yr
Clinical Trials Manager - Oncore Data Job no: 493887 Work type: Managerial Location: Oklahoma City Categories: Technology/Research Pay Range: Targeted salary from $55,800 - $72,600 annually, based on ...
CLINICAL TRIALS MANAGER
Raritan, NJ · On-site
$44/hr
Minimum of 8 years direct clinical research experience, of which a minimum of 4 years clinical research supervisory or management capacity with budgetary responsibility. * Knowledge of applicable ...
CLINICAL TRIALS MANAGER
Raritan, NJ · On-site
$44/hr
Minimum of 8 years direct clinical research experience, of which a minimum of 4 years clinical research supervisory or management capacity with budgetary responsibility. * Knowledge of applicable ...
Clinical Trials Manager information
See salary details
$28.85 - $34.97
4% of jobs
$34.97 - $41.08
6% of jobs
$41.08 - $47.20
7% of jobs
$51.79 is the 25th percentile. Wages below this are outliers.
$47.20 - $53.32
9% of jobs
$53.32 - $59.44
15% of jobs
The median wage is $62.14 / hr.
$59.44 - $65.56
18% of jobs
$69.92 is the 75th percentile. Wages above this are outliers.
$65.56 - $71.68
21% of jobs
$71.68 - $77.80
7% of jobs
$77.80 - $83.92
6% of jobs
$83.92 - $90.03
3% of jobs
$90.03 - $96.15
2% of jobs
$28
$62
$96
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.
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States with the most job openings for Clinical Trials Manager jobs include:
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Full-time
Medical, Dental, Vision, Life, Retirement
Posted 5 days ago
Georgetown University rating
7.6
Based on 21 frontline employees who took The Breakroom Quiz
291st of 627 rated colleges and universities
Job description
Georgetown University comprises two unique campuses in the nation's capital. With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world.
Requirements
Job Overview
Clinical Trials Manager, Department of Neurology/Memory Disorders - Georgetown University. Participates in clinical trial set up, execution, documentation, education/recruitment, and provides general data management of the most complex clinical studies in the Department of Neurology, Memory Disorders Program. As clinical trials manager, responsibilities include review and mastery of clinical research documents (protocols, case report forms, reports and statistical analysis), monitoring recruitment and retention, adherence to study visit schedule, timely data entry (develops data management plans), compliance with all study procedures including close-out and training of other staff members on protocol measures and GU clinical research policies as needed. Responsible for patient cognitive testing (minimum two-years cognitive testing experience necessary), caregiver communication and interview, chart review and data organization using various web-based databases.
The Clinical Trials Manager will also prepare for and facilitate research and monitoring visits as well as administer cognitive testing to subjects. The incumbent will manage multiple local and multi-center clinical trials and will need to be detail-oriented with a solid base of management skills and interpersonal skills. The individual is expected to have working knowledge of compliance policies with respect to the clinical regulatory environment and requires little to no supervision to perform all job functions. Acts as liaison with clinicians, pharmaceutical companies and the federally-funded Alzheimer's Disease Research Institute (ATRI) to implement studies and to meet all data timelines, in part to ensure timely and accurate study payments to GU. Corresponds directly with study sponsors to facilitate subject participation, submits subject visit information and resolves data queries. The position will provide support to the Principal Investigator (PI), co-investigators and all other study collaborators for neurology clinical trials. The manager is also responsible for maintaining and facilitating regulatory documents, including IRB submissions, together with the Regulatory Manager. The clinical trials manager will also prepare dynamic training guides to promote seamless onboarding for new staff members in the Memory Disorders Program and will work diligently - including troubleshooting for all Memory Disorders staff- within the OnCore system to manage study visit data and study visit payments to participants. The manager will be required to obtain and retain all necessary certifications in order to perform the position effectively.
Work Interactions
Works as part of a team to establish effective management of clinical trials within the Department of Neurology, Memory Disorders Program. Recruit, conduct, establish and organize, document and maintain approval for these trials. The position will provide support to the Principal Investigator (PI), co-investigators and all other study collaborators for Memory Disorders Program clinical trials. Works with PIs, fellows, subjects and team members to conduct safe, accredited clinical trials in the Department of Neurology.
Operates with a strong understanding of current GU policies and SOPs related to research and compliance. Works under the direct supervision of the Research Director Neurology/Memory Disorders. This position
also requires interaction with patients, sponsors and CROs.
Requirements and Qualifications
Bachelor's or Master's degree and 3-5 years of experience or equivalent relevant work experience; e.g. each year or work experience may be substituted for each year of education required
Excellent organizational and communication skills with ability to work independently and collaboratively with investigators and subjects
Attention to detail is critical and must be self-directed with a solid base of management skills.
Must be able to manage multiple tasks
Must be able to demonstrate successful track records using analytical, organizational and problem-solving skills
Excellent interpersonal skills and ability to communicate professionally and clearly.
Solids writing skills include grammar, punctuation, composition and spelling.
Computer proficiency essential, with demonstrated knowledge of PC software programs including Windows, MS Office, internet and email.
Work Mode Designation
This position has been designated as On-Campus. Please note that work mode designations are regularly reviewed in order to meet the evolving needs of the University. Such review may necessitate a change to a position's mode of work designation. Complete details about Georgetown University's mode of work designations for staff positions can be found on the Department of Human Resources website:https://hr.georgetown.edu/mode-of-work-designation.
Pay Range:
The projectedsalary or hourly pay range for this position which represents the full range of anticipated compensation is:
$44,022.00 - $73,406.80Compensation is determined by a number of factors including, but not limited to, the candidate's individual qualifications, experience, education, skills, and certifications, as well as the University's business needs and external factors.
Current Georgetown Employees:
If you currently work at Georgetown University, please exit this website and login to GMS (gms.georgetown.edu) using your Net ID and password. Then select the Career worklet on your GMS Home dashboard to view Jobs at Georgetown.
Submission Guidelines:
Please note that in order to be considered an applicant for any position at Georgetown University you must submit a resumefor each position of interest for which you believe you are qualified. Documents are not kept on file for future positions.
Need Assistance:
If you are a qualified individual with a disability and need a reasonable accommodations for any part of the application and hiring process, please visit the Office for Equal Opportunity Compliance website for general information about requesting accommodations, as well as information about requesting accommodations specifically for applicants. You also can also contact the Office for Equal Opportunity Compliance at (202) 687-4798 or oeoc@georgetown.edu.
Need some assistance with the application process? Please call 202-687-2500. For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works website.
EEO Statement:
GU is an Equal Opportunity Employer. All qualified applicants are encouraged to apply, and will receive consideration for employment without regard to age, citizenship, color, disability, family responsibilities, gender identity and expression, genetic information, marital status, matriculation, national origin, race, religion, personal appearance, political affiliation, sex, sexual orientation, veteran status, or any other characteristic protected by law.
Benefits:
Georgetown University offers a comprehensive and competitive benefit package that includes medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts and an array of voluntary insurance options. You can learn more about benefits and eligibility on the Department of Human Resources website.
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About Georgetown University
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Georgetown University, located in Washington, DC, US, is one of the oldest and most prestigious institutions in the higher education industry. As a private research university, Georgetown offers a wide range of programs and services in various academic disciplines. The institution was founded in 1789 by John Carroll, America's first Catholic bishop, and carries a rich history ingrained in Jesuit values like cura personalis (care for the whole person) and men and women for others. The mission of Georgetown University is to shape individuals who seek to better the world and its diverse cultures, thus creating a positive impact on societies. It is recognized for its fruitful legacy in academics, commitment to social justice, and fostering of global awareness and understanding among its students.
Industry
Colleges, universities, and professional schools
Company size
5,001 - 10,000 Employees
Headquarters location
Washington, DC, US
Year founded
1789