Ripple Effect este o firmă de consultanță înființată în 2003, care sprijină organizații federale, organizații din sectorul privat și organizații nonprofit prin expertiză și talente specializate. Echipa sa multidisciplinară activează în domenii precum managementul programelor, serviciile tehnice și științifice, comunicarea și informarea publică, cercetarea și evaluarea, precum și transformarea digitală. Compania își ajută clienții să elaboreze și să implementeze politici, programe și îmbunătățiri operaționale, adaptându-și abordarea la nevoile diferitelor industrii și medii organizaționale. Ripple Effect pune, de asemenea, accent pe diversitate și incluziune ca parte a culturii sale organizaționale.
Human Subjects Research Analyst
Review DHS-supported biomedical research protocols for regulatory compliance and support human research protection teams. Contribute to quality assurance, protocol management, and recommendations for executive leadership.
Descriere
- Review human subjects research submissions, including amendments, continuing reviews, award continuations, and final study reports.
- Assist with developing and reviewing DHS-supported research protocols for regulatory compliance.
- Monitor compliance with federal, DHS, state, local, and other human subjects protection requirements.
- Prepare regulatory reviews using standardized checklists.
- Flag deficiencies and noncompliance in protocol submissions.
- Help the DHS Human Research Protection Group Lead Analyst and federal staff assess complex regulatory and ethical issues.
- Support administrative reporting of recommendations to executive management.
- Maintain protocol records and related information management systems.
- Collaborate with senior scientists on a Human Research Protection Group team.
Cerințe
- Hold a bachelor’s degree in life science, biomedical science, or a related field.
- Have six years of relevant professional experience.
- Apply laws, regulations, policies, procedures, and guidance governing human subjects research and cadaver use.
- Make regulatory review recommendations that address deficiencies or noncompliance in human research.
- Bring professional experience in quality control or quality assurance.
- Communicate effectively in writing and verbally.
- Work effectively with diverse colleagues and collaborate across teams.
- Prioritize multiple projects in a fast-paced, deadline-driven setting.
- Demonstrate strong attention to detail and follow instructions reliably.
- Show commitment to quality and compliance.
- Have intermediate proficiency with Microsoft Office productivity software.
- Have intermediate proficiency with Microsoft Teams and SharePoint.
- Be able to travel locally, regionally, or nationally.
- A master’s degree in life science, biomedical science, or a related field is preferred.
- Relevant certifications such as CIP or SOCRA are preferred.
- CITI training consistent with local IRB policy is preferred.
- Experience serving on or administering an IRB is preferred.
- Experience as a government contractor supporting biomedical or health research programs within DHS or other federal systems is preferred.
- Intermediate experience using generative AI, automation, and structured data for labor estimates, pricing analytics, proposal benchmarking, and decision support—with appropriate human oversight and quality controls—is preferred.
Beneficii
- Competitive compensation.
- Comprehensive benefits.
- Programs that support work-life balance.
- Personalized preference programs.
- Flexible work arrangements.