Clinical Program Manager
$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 ...
$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 ...
$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 ...
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
Quick apply
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
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 ...
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:
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:
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:
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:
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:
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
Quick apply
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
Bethesda, MD · On-site
$72K - $141K/yr
Our expert team delivers the latest therapies, access to 300+ clinical trials, and state-of-the-art ... Manage schedule for clinic nurses, medical assistants (if applicable), lab (If applicable) and ...
Bethesda, MD · On-site
$72K - $141K/yr
Our expert team delivers the latest therapies, access to 300+ clinical trials, and state-of-the-art ... Manage schedule for clinic nurses, medical assistants (if applicable), lab (If applicable) and ...
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
Quick apply
... trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess ... Provides education regarding adjustment to illness and managing protocol related logistics.
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
$150K - $225K/yr
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
$150K - $225K/yr
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
Phase I through post-marketing experience across anterior segment and retina trials * Clinical Ophthalmology, Optometry, and clinical trial expertise Primary Purpose The Project Delivery Manager (PDM ...
Phase I through post-marketing experience across anterior segment and retina trials * Clinical Ophthalmology, Optometry, and clinical trial expertise Primary Purpose The Project Delivery Manager (PDM ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
The Program Manager or Director will oversee a coordinated portfolio spanning rapid demonstration trials, parallel development of multiple antigen classes and vaccine platforms, scalable GMP ...
Bethesda, MD · On-site
$105K - $115K/yr
The Data and Analytics Manager is responsible for leading the day-to-day functions of a core Data ... trials, across military treatment facilities, academic institutions, and other sites nationwide.
Bethesda, MD · On-site
$105K - $115K/yr
The Data and Analytics Manager is responsible for leading the day-to-day functions of a core Data ... trials, across military treatment facilities, academic institutions, and other sites nationwide.
Washington, DC · On-site
$160K - $193K/yr
The Pharmacy Manager for Infusion Services will be responsible for leading and nurturing individual ... Participate in clinical trials, research protocols, and performance improvement initiatives.
Washington, DC · On-site
$160K - $193K/yr
The Pharmacy Manager for Infusion Services will be responsible for leading and nurturing individual ... Participate in clinical trials, research protocols, and performance improvement initiatives.
| Criteria | Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in trial management, knowledge of regulations | Bachelor's degree, clinical research experience, regulatory knowledge |
| Work Environment | Oversees multiple trials, manages teams, coordinates with sponsors | Handles daily trial activities, patient interactions, data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.

$85K - $141K/yr
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 22 days ago
7.7
Based on 27 frontline employees who took The Breakroom Quiz
42nd of 72 rated business consultants
Job Family:
Clinical Trial Operations
Travel Required:
Clearance Required:
What You Will Do:
We are currently searching for a Clinical Program Manger to support complex clinical research programs by coordinating investigators, research teams, oversight offices, regulatory agencies, partner institutions, and other key stakeholders to ensure studies run efficiently. This is a full-time opportunity located in Bethesda, MD.
Provide end-to-end project management for clinical research, including planning, execution, monitoring, and closeout of studies and portfolios.
Develop and maintain project management plans, work plans, schedules, and performance metrics to track progress, timelines, deliverables, and resource allocation.
Coordinate operational and startup activities for clinical trials, including feasibility assessments, site coordination for multi-center trials, and study activation.
Facilitate project meetings, track action items, and ensure effective communication among stakeholders, leadership, and collaborating institutions.
Monitor study progress, enrollment metrics, and portfolio performance, identifying risks, barriers, and opportunities for improvement.
Support protocol development, IRB and regulatory submissions, amendments, and compliance with clinical trial requirements and milestones.
Develop and implement risk management strategies, including mitigation plans and resolution of operational, regulatory, and programmatic issues.
Support audits, inspections, and monitoring visits, ensuring readiness and compliance with applicable standards and guidelines.
Assist with financial management activities, including budget development, expenditure tracking, forecasting, and reporting.
Serve as a liaison between research programs, regulatory offices, and partners, preparing briefings, reports, and communication materials for leadership.
Support acquisition planning, contractor oversight, and strategic initiatives, including performance tracking and process improvement efforts.
Prepare and deliver routine and ad hoc reports such as portfolio status, risk management, financial summaries, regulatory tracking, and annual program reports.
What You Will Need:
Master's degree in health and medical administrative services, nursing, or a related field.
Minimum of FOUR (4) years of experience supporting clinical research programs.
Experience supporting complex clinical research portfolios and coordinating across stakeholders.
Experience with clinical trial management systems and research databases.
Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or similar partnerships.
Experience supporting NIH, NCI, academic medical centers, or federally funded research programs.
Ability to manage multiple projects, timelines, and stakeholders simultaneously.
Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates with an active public trust or suitability are preferred.
What Would Be Nice To Have:
Certifications in any of the following: SOCRA, FAC-P/M, FAC-COR, and/or PMP Certification.
Strong project management, coordination, and communication skills.
Association of Clinical Research Professionals (ACRP) certification.
Experience in clinical trial design, feasibility assessments, and regulatory processes.
Experience supporting multi-site or multi-center clinical trials.
What We Offer:
Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.
Benefits include:
Medical, Rx, Dental & Vision Insurance
Personal and Family Sick Time & Company Paid Holidays
Parental Leave
401(k) Retirement Plan
Group Term Life and Travel Assistance
Voluntary Life and AD&D Insurance
Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts
Transit and Parking Commuter Benefits
Short-Term & Long-Term Disability
Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities
Employee Referral Program
Corporate Sponsored Events & Community Outreach
Care.com annual membership
Employee Assistance Program
Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)
Position may be eligible for a discretionary variable incentive bonus
About Guidehouse
Guidehouse is an Equal Opportunity Employer-Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.
Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.
If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.
All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or guidehouse@myworkday.com. Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.
If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse's Ethics Hotline. If you want to check the validity of correspondence you have received, please contact recruiting@guidehouse.com. Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant's dealings with unauthorized third parties.
Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.
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Business management consulting
10,000+ Employees
Falls Church, VA, US
2005