Project Manager/Senior Human Subject Protection Scientist
- Blue Bell
- Clinical Project Management
- ICON Full Service & Corporate Support
- Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
Project Manager/Senior Human Subject Protection Scientist-Fort Detrick MD-Onsite
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
***This position is contingent upon a future contract award and is not available for immediate hire. ***
Location onsite: Fort Detrick, Frederick MD
We are seeking an experienced Project Manager Human Subject Protection Scientist III to supervise contract personnel and support the US Army Medical Research and Development Command (USAMRDC) by ensuring compliance with human subjects protection and cadaver use regulations. This role combines project management, regulatory oversight, policy development, and quality assurance.
What you will be doing:
- Project Management & Leadership – Serve as the on-site PM, supervising contract personnel at OHARO and OHRO. Maintain a small caseload of protocols to stay current with processes and provide effective guidance.
- Protocol Review & Compliance – Conduct initial administrative reviews of research submissions, ensuring compliance with Federal, DoD, DA, state, host nation, and USAMRDC regulations. Identify deficiencies and provide regulatory recommendations.
- Policy & Procedure Development – Assist in updating policies and guidelines while providing regulatory guidance to investigators and research staff.
- Education & Training – Review and update training materials to reflect the latest human subjects protection and cadaver use regulations.
- Quality Assurance – Maintain and update protocol tracking systems, ensuring accuracy in automated compliance databases.
- Performance Improvement – Participate in workflow optimization initiatives, contributing to standard operating procedures (SOPs) and work instructions.
Your profile:
- Bachelor’s degree required, Master’s preferred
- 5+ years of experience in human research protection, IRB protocol review, regulatory compliance, or quality assurance.
- Project management experience, including staff supervision and workflow oversight.
- Strong knowledge of Federal, DoD, DA, and USAMRDC human subjects’ protection and cadaver use regulations, including the Common Rule and HIPAA.
- Certified IRB Professional (CIP) or Certified IRB Manager (CIM) preferred
- Experience conducting regulatory reviews, IRB pre-reviews, and compliance assessments.
- Proven ability to develop policies, procedures, and training programs for regulatory compliance.
- Strong leadership, problem-solving, and communication skills, with experience in performance improvement initiatives.
Location onsite: Fort Detrick, Frederick MD
#LI-TG2
#LI-Onsite
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high
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