Clinical Research Specialist – Leading Protocol Development

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DLH Corporation

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1997

🏥 Healthcare

💼 Consulting

🎖️ Defense

Healthcare • Consulting • Defense

DLH Corporation is a company that addresses health and national security challenges through digital transformation, science research and development, and systems engineering. It offers solutions for federal programs by leveraging expertise in public health, performance evaluation, artificial intelligence, advanced analytics, cloud-based applications, and telehealth systems. DLH is committed to responsible citizenship and community service through its DLH Cares initiative. Additionally, DLH provides critical systems engineering and services for military systems and promotes workplace excellence, as evidenced by its Great Place To Work® Certification.

📋 Description

• Manage protocol teams as they design, implement, and report results from clinical trials • Lead protocol development, study start-up, and study conduct activities • Lead development of protocol documents, incorporating input from subject matter experts and investigators • Develop informed consent forms • Develop and manage study-specific ancillary documents, including manuals of procedure and site training materials • Manage and communicate study progress and activities • Drive resolution of issues encountered with sites during all study phases • Partner with clinical data management, statisticians, laboratory, and other cross-functional teams • Develop and implement processes to mitigate impediments to protocol development and implementation • Assess processes and implement solutions to improve efficiency • Provide coaching and knowledge transfer to team members • Attend an annual network meeting in the DC area

🎯 Requirements

• Master’s degree in public health, social sciences, or related discipline strongly preferred, with at least two years of experience in the design, development, and conduct of Phase I–III clinical trials • Bachelor's degree may be accepted with at least five years of experience in the design, development, and conduct of Phase I–III clinical trials • Experience leading protocol development, including writing clinical research protocols and ancillary documents, is required • Experience with HIV, hepatitis, and/or tuberculosis trials is preferred • Excellent verbal communication and organization skills • Ability to follow detailed work instructions • Strong problem-solving and decision-making skills • Ability to handle multiple tasks simultaneously and work collaboratively

🏖️ Benefits

• Basic compensation of $80,000–$90,000 yearly salary • Performance incentives and program-specific awards may be included • Personal Time Off (PTO) • Medical insurance • Dental insurance • Vision insurance • Supplemental life insurance with AD&D • Short-term disability • Long-term disability • Flexible spending accounts • Parental leave • Legal services • 401(k) Retirement Plan with matching component • Career development training • Best-in-class e-learning suite for formal and informal learning • Professional and technical certification preparation • Education assistance at accredited institutions