Project Manager - Clinical Trial Operations Exp. Req. (Job 1421)
DLH United States · $90K–$110K/yr
Technology, Information and Internet · 1,001-5,000 employees
About the role
The Project Manager will oversee end-to-end clinical trial operations, including study start-up, site coordination, and protocol implementation. They are responsible for managing project scope, schedules, resource plans, and ensuring adherence to quality standards throughout the project lifecycle.
What they look for
Requirements
Candidates must hold a Bachelor's degree in a relevant field with at least 4 years of experience, or a Master's degree with 2 years of experience in clinical trial operations. Strong knowledge of regulatory requirements such as GCP, ICH, and FDA/NIH guidelines is required.
Benefits
Full description
About Us
DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation. Our experts in public health, performance evaluation, and health operations solve the complex problems faced by civilian and military customers alike by leveraging advanced tools – including digital transformation, artificial intelligence, data analytics, cloud enablement, modeling, and simulation, and more. DLH is dedicated to the idea that “Your Mission is Our Passion” and brings a unique combination of government sector experience, proven methodology, and unwavering commitment to innovation to improve the lives of millions.
Overview
DLH is seeking a career-level Project Manager (PM) with strong clinical research expertise to join our talented and innovative team in support of our Public Health and Scientific Research (PHSR) Operating Center. The PM will provide primary project management oversight for clinical research studies for the Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections (ACTG) Clinical Trials Network.
Responsibilites
- Responsible for the performance of relatively small technical projects or a definable portion of a larger technical program in accordance with contract requirements and company policies, procedures and guidelines.
- Directs and supervises all support resources for the performance of project assignments and activities.
- Manages the technical direction of a project through the design, implementation, and testing in accordance with project objectives.
- Responsible for all aspects of the development and implementation of assigned projects and provides a single point of contact for those projects.
- Takes projects from original concept through final implementation.
- Interfaces with all areas affected by the project, including end users, computer services, and client services.
- Defines project scope and objectives.
- Develops detailed work plans, schedules, project estimates, resource plans, and status reports.
- Conducts project meetings and is responsible for project tracking and analysis.
- Ensures adherence to quality standards and reviews project deliverables.
- Manages the integration of vendor tasks and tracks and reviews vendor deliverables. Provides technical and analytical guidance to the project team.
- Recommends and takes action to direct the analysis and solutions of problems.
- Oversees end-to-end clinical trial operations, including study start-up, site coordination, protocol implementation, enrollment tracking, and study close-out.
- Conducts project meetings and maintains overall responsibility for project tracking, analysis, and issue remediation.
Qualifications
- Bachelor’s degree in public health, life sciences, health administration, or a related field with 4+ years of experience in clinical trial operations or Master’s degree with 2+ years of experience in clinical trial operations (Preferred).
- Strong knowledge of regulatory requirements (GCP, ICH, FDA/NIH guidelines).
- Proven ability to manage complex projects collaboratively.
- Excellent communication, organizational, and problem-solving skills.
Preferred Qualifications
- PMP certification preferred
- Experience supporting clinical trials in infectious diseases or related therapeutic areas
- Previous engagement with large, multi-site clinical research programs or networks.
Basic Compensation: $$90,000 - $110,000 yearly salary
The salary range listed reflects what we reasonably expect to pay for this role at the time of posting. The final offer may vary based on skills, experience, geographic location, market conditions, and internal equity. Additional compensation may include performance incentives and program-specific awards. We do not use salary history to determine compensation, in line with applicable law.
Benefits
DLH Corp offers our employees an excellent benefits package, including Personal Time Off (PTO), medical, dental, vision, supplemental life with AD&D, short and long-term disability, flexible spending accounts, parental leave, legal services, and more. We want our employees to save for their future; therefore, we offer a 401(k) Retirement Plan, which includes a matching component. DLH is dedicated to your career development, providing training to help drive success, with access to our best-in-class e-learning suite for formal and informal learning, professional and technical certification preparation, and education assistance at accredited institutions.
#LI-REMOTE
EEO
DLH Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment. DLH will provide reasonable accommodation to individuals with disabilities and disabled Veterans who need assistance to apply.
DLH is committed to maintaining a fair and authentic interview process
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