Clinical Program Manager

Dovel Technologies, Inc; Bethesda (MD); On-site; USD 85,000 - 141,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

Parental Leave

Tuition Reimbursement

Job summary

Dovel Technologies, Inc. in Bethesda, MD seeks a Clinical Program Manager to coordinate investigators, research teams, oversight offices, and regulatory bodies to ensure studies run efficiently.

You will provide end-to-end project management for clinical research, develop PM plans, monitor timelines and metrics, and support multi-center trial activation and regulatory milestones.

Qualifications

• Master’s degree in health administration, nursing, or a related field.
• Four+ years of experience supporting clinical research programs.
• Experience coordinating across investigators, regulatory bodies, and stakeholders.
• Experience with clinical trial management systems and research databases.

Responsibilities

• Provide end-to-end project management for clinical studies and portfolios.
• Develop and maintain PM plans, schedules, and performance metrics to track progress and resources.
• Coordinate startup activities and site coordination for multi-center trials and study activation.
• Support protocol development, IRB submissions, amendments, and regulatory milestones.
• Prepare routine and ad hoc portfolio and program status reports for leadership.

Education

Master’s degree in health administration, nursing, or related field

Tools

Clinical Trial Management Systems

Research databases

Job description

## Clinical Program ManagerApplylocations: US - MD, Bethesdatime type: Full timeposted on: Posted Todayjob requisition id: 42233**Job Family:**Clinical Trial Operations**Travel Required:**None**Clearance Required:**Ability to Obtain Public Trust**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.* Support complex clinical research portfolios by coordinating activities across investigators, research teams, regulatory bodies, and stakeholders 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.The annual salary range for this position is $85,000.00-$141,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.**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