Biostatistics and Clinical Trials Advisor The Opportunity: To achieve an organization's mission ... You will be responsible for managing incoming requirements, facilitating engagements within offices ...
Biostatistics and Clinical Trials Advisor The Opportunity: To achieve an organization's mission ... You will be responsible for managing incoming requirements, facilitating engagements within offices ...
We are exploring the addition of an experienced Clinical Trials Program Manager to provide leadership in planning, coordinating, and executing decentralized clinical trials (DCTs) in support of the ...
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We are exploring the addition of an experienced Clinical Trials Program Manager to provide leadership in planning, coordinating, and executing decentralized clinical trials (DCTs) in support of the ...
Share Biostatistics and Clinical Trials Advisor The Opportunity: To achieve an organization ... You will be responsible for managing incoming requirements, facilitating engagements within offices ...
Share Biostatistics and Clinical Trials Advisor The Opportunity: To achieve an organization ... You will be responsible for managing incoming requirements, facilitating engagements within offices ...
Clinical Research Coordinator 1
Washington, DC · On-site
$67K/yr
Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials. * Collaborate with Data Manager(s ...
Clinical Research Coordinator 1
Washington, DC · On-site
$67K/yr
Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials. * Collaborate with Data Manager(s ...
Clinical Research Coordinator
Washington, DC · On-site
$27.50 - $36.75/hr
Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of ...
Clinical Research Coordinator
Washington, DC · On-site
$27.50 - $36.75/hr
Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of ...
Clinical Research Manager
$105K - $120K/yr
About the Position The Clinical Research Manager oversees on-site research operations to include supervision of the conduct of clinical trials, recruitment of new research studies and investigators ...
Clinical Research Manager
$105K - $120K/yr
About the Position The Clinical Research Manager oversees on-site research operations to include supervision of the conduct of clinical trials, recruitment of new research studies and investigators ...
Clinical Trial Physician
Washington, DC · On-site
$110 - $140/hr
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
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Clinical Trial Physician
Washington, DC · On-site
$110 - $140/hr
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
Clinical Trial Physician
Washington, DC · On-site
$110 - $140/hr
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
Clinical Trial Physician
Washington, DC · On-site
$110 - $140/hr
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
Clinical Research Manager
Bethesda, MD · On-site
$105K - $120K/yr
About the Position The Clinical Research Manager oversees on-site research operations to include supervision of the conduct of clinical trials, recruitment of new research studies and investigators ...
Clinical Research Manager
Bethesda, MD · On-site
$105K - $120K/yr
About the Position The Clinical Research Manager oversees on-site research operations to include supervision of the conduct of clinical trials, recruitment of new research studies and investigators ...
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...
Participates in the planning, implementation and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract Research Organization (CRO) partners, if applicable. Manage ...
Participates in the planning, implementation and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract Research Organization (CRO) partners, if applicable. Manage ...
Study Builder / Clinical Trials / REDCap with Security Clearance
Bethesda, MD · On-site
$120K - $126K/yr
This role involves translating clinical study requirements into technical system solutions, performing user acceptance testing (UAT), and managing technical implementations for clinical trials.
Study Builder / Clinical Trials / REDCap with Security Clearance
Bethesda, MD · On-site
$120K - $126K/yr
This role involves translating clinical study requirements into technical system solutions, performing user acceptance testing (UAT), and managing technical implementations for clinical trials.
... in ongoing clinical trials for life threatening illnesses with the NIH in Bethesda, MD. The ... Provides education regarding adjustment to illness and managing protocol related logistics.
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... in ongoing clinical trials for life threatening illnesses with the NIH in Bethesda, MD. The ... Provides education regarding adjustment to illness and managing protocol related logistics.
... in ongoing clinical trials for life threatening illnesses with the NIH in Bethesda, MD. The ... Provides education regarding adjustment to illness and managing protocol related logistics.
Quick apply
... in ongoing clinical trials for life threatening illnesses with the NIH in Bethesda, MD. The ... Provides education regarding adjustment to illness and managing protocol related logistics.
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Clinical Program Manager
Bethesda, MD · On-site
$85K - $141K/yr
Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...
Clinical Program Manager
Bethesda, MD · On-site
$85K - $141K/yr
Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Drive global clinical trials from first site activation to final patient visit-own the strategy ... Required Experience * 2+ years of global study management experience * Experience across multiple ...
Clinical Program Manager
Bethesda, MD · On-site
$85K - $141K/yr
Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...
Clinical Program Manager
Bethesda, MD · On-site
$85K - $141K/yr
Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials * Lead day-to-day study management activities across study startup, conduct, maintenance, and ...
Requirements Job Overview The Clinical Research Coordinator I (CRCI) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of ...
Requirements Job Overview The Clinical Research Coordinator I (CRCI) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of ...
Clinical Trials Manager information
See Reston, VA salary details
$30.01 - $36.38
4% of jobs
$36.38 - $42.74
6% of jobs
$42.74 - $49.11
7% of jobs
$53.88 is the 25th percentile. Wages below this are outliers.
$49.11 - $55.47
9% of jobs
$55.47 - $61.84
15% of jobs
The median wage is $64.65 / hr.
$61.84 - $68.20
18% of jobs
$72.74 is the 75th percentile. Wages above this are outliers.
$68.20 - $74.57
21% of jobs
$74.57 - $80.94
7% of jobs
$80.94 - $87.30
6% of jobs
$87.30 - $93.67
3% of jobs
$93.67 - $100.03
2% of jobs
$30
$65
$100
How much do clinical trials manager jobs pay per hour?
What does a clinical trials manager do?
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 some common challenges faced by clinical trials managers and how can they be addressed?

Full-time
Medical, Life, Retirement, PTO
Posted 8 days ago
Booz Allen Hamilton rating
8.8
Based on 48 frontline employees who took The Breakroom Quiz
13th of 72 rated business consultants
Job description
The Opportunity:
To achieve an organization's mission, leaders need strong team members who can create processes, communicate requirements, and develop innovative solutions throughout the execution of the mission. Whether completing an immediate task, recognizing a process gap, recommending a solution, or flexing to support an immerging requirement, our clients need a consultant who can help manage operations while managing responses to external inquiries in a timely manner. That is why we need you, an experienced Biostatistics and Clinical Trials Advisor, to provide technical expertise and project development for emerging opportunities within healthcare.
As part of our team, you'll serve as a strategic technical consultant to the Advanced Research Projects Agency for Health (ARPA-H), helping conceptualize, create, and execute advanced government-funded research and development programs to accelerate better health outcomes for everyone. Work with world-class scientists and engineers to support the development of high-impact solutions to society's most challenging health problems. Leverage technical expertise to provide strategic assessments of new technologies in support to senior ARPA-H decision makers. Maintain responsibility for producing and presenting findings and recommendations to a team of colleagues and clients on the feasibility and potential impact of future research programs, assisting with the management of current programs, and facilitating commercialization of successfully developed technologies.
You'll serve as a Biostatistics and Clinical Trials Advisor helping clients to develop stakeholder management strategies, establish new business processes, and complete research and analysis to determine viable solutions. You will be responsible for managing incoming requirements, facilitating engagements within offices and across the Agency, and being readily available to shift your focus to fulfill emerging client requests. Your attention to detail, flexibility, communication skills, understanding of the client's mission, and problem-solving will enable the mission's success.
What You'll Work On:
Support strategy development and program execution for biostatistics, clinical trials, artificial intelligence/machine learning for clinical trials, and computational modeling initiatives
Offer deep technical insight into the design and evaluation of clinical trials, including innovative approaches such as adaptive, platform, digital twins, or in silico clinical trial simulations
Advise on quantitative and statistical modeling for pharmacology, including Bayesian, frequentist, and empirical modeling approaches
Evaluate the credibility and standards for computational and physicsbased models for drugs, biologics, and advanced therapeutics, such as Quantitative Systems Pharmacology, Pharmacokinetic/Pharmacodynamic, or digital twin
Coordinate with federal stakeholders and other interagency partners to support the development, evaluation, and transition of new drug clinical trial projects
Evaluate the conceptual and technical soundness of research programs spanning biostatistics, clinical trials, artificial intelligence/machine learning for clinical trials, and computational modeling
Assist in defining program goals, technical milestones, budgets, and performer expectations for high-impact scientific initiatives; conduct technical reviews of performer progress to ensure alignment with ARPA-H objectives
Interact with clients, government officials, and other executives in various sectors
Join us. The world can't wait.
You Have:
3+ years of experience building physics-based and mechanistic models for drugs or biologics
1+ years of experience supporting new drug clinical trials of any phase for products regulated by FDA CDER or CBER, such as drugs, biologics, or advanced therapies
Experience with Bayesian, frequentist, and empirical methods
Experience supporting and advising government leadership or federal research programs
Knowledge of biostatistics and statistical modeling
Knowledge of clinical trial design
Ability to manage budgets, technical milestones, and multidisciplinary research efforts across multi-site or multi-performer programs
Doctorate degree in Biostatistics, Bioinformatics, Computational Biology, Epidemiology, or a Biomedical or Health Sciences field
Nice If You Have:
Experience with disease- or patient-specific digital twin models
Experience with in silico clinical trial simulations, specifically clinical trial optimization via in silico simulations
Experience with synthetic data generation to augment real control patients in clinical trials
Experience in the development or evaluation of artificial intelligence/machine learning approaches
Experience with innovative clinical trial design approaches such as adaptive and platform trial designs
Experience with assessing the credibility or development of standards for computational and physics-based models such as Quantitative Systems Pharmacology (QSP) and Pharmacokinetic/Pharmacodynamic (PK/PD) models
Experience operating within a government environment and supporting senior federal leaders
Ability to manage multiple priorities at once
Possession of excellent communication skills
Compensation
At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen's benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page.
Salary at Booz Allen is determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The projected compensation range for this position is $86,800.00 to $198,000.00 (annualized USD). The estimate displayed represents the typical salary range for this position and is just one component of Booz Allen's total compensation package for employees. This posting will close within 90 days from the Posting Date.Identity Statement
As part of the hiring process, we will ask you to complete an identity verification process that leverages advanced biometrics and artificial intelligence to ensure authenticity and protect against identity fraud. You are expected to be on camera during interviews and assessments. We reserve the right to take your picture to verify your identity and prevent fraud.
Candidate AI Usage Policy
AI is a part of our daily work at Booz Allen, and we are committed to the responsible and ethical use of AI tools. However, we want to ensure a fair candidate process based on your own skills and knowledge. As part of this commitment, the use of artificial intelligence (AI) or other tools to assist with responses during interviews (whether in-person or virtual) is prohibited unless permission is explicitly provided.
Work Model
Our people-first culture prioritizes the benefits of collaboration, whether it occurs in person or virtually. To support engagement and effective communication, employees working virtually are generally expected to have their cameras on during meetings.
Remote: If this position is listed as remote, there may still be occasions when you are required to work in person at a Booz Allen or customer facility.
Hybrid: If this position is listed as hybrid, you will be expected to work from a Booz Allen facility frequently, in alignment with leadership expectations and the needs of the role. You may also be required to work from or visit a customer facility.
Onsite: If this position is listed as onsite, work will primarily be performed at a Booz Allen office or customer facility, where employees will collaborate directly with colleagues and customers as required by the role.
Commitment to Non-Discrimination
All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, local, or international law.
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About Booz Allen Hamilton
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Booz Allen Hamilton is a leading provider of management and technology consulting services to the US government in defense, intelligence, and civil markets. Headquartered in McLean, Virginia, the firm also serves major corporations, institutions, and not-for-profit organizations. Founded in 1914 by Edwin G. Booz, the company has a long-standing tradition of helping clients achieve success by delivering a wide range of consulting services that include strategic planning, human capital and learning, communication, systems development, and others. The company's mission is to empower people to change the world, and it has a reputation for maintaining the highest standards of integrity and-excellence.
Industry
It services
Company size
10,000+ Employees
Headquarters location
McLean, VA, US
Year founded
1914