Provide administrative support in biomedical human subjects research for DHS. Ensure ethical standards in research protocols and offer customer support for stakeholders.
Responsibilities
Provide timely and professional customer service and support by delivering accurate information, assistance, and documents to principal investigators, study team members, program manager, approval authorities and other DHS stakeholders.
Actively monitor a central inbox for new emails, prioritizing urgent or important messages for immediate attention; identify and escalate complex or sensitive emails to the appropriate POC for further handling.
Update and manage human research protocol files from intake and throughout the lifecycle and the information management systems used to track protocol review related data and other information.
Coordinate active backup of working materials to facilitate review of future actions by team members.
Contribute to the development of training and education materials.
Other related duties, as assigned
Requirements
BA/BS in a life science, biomedical, or related field
2 years of relevant professional experience
Basic working knowledge of human subjects' protections, regulations, and guidelines
Experience in maintaining and tracking data and progress of regulatory reviews with ability to organize work assignments
Excellent written and oral communication skills and the ability to work well with various individuals and collaborate across teams throughout a dynamic and diverse research enterprise.
Ability to prioritize among multiple tasks in a fast-paced, deadline-driven environment, relying on your own resources and initiative.
Strong skills in using MS Office software and shared workspaces such as SharePoint and OneDrive.
Must work effectively in a team environment.
Benefits
Competitive pay
Exceptional benefits
Range of work/life programs based on employment classification and personalized preferences
Clinical Research Associate ensuring sites conduct studies and reporting data accurately. Monitoring, site management, and collaboration with the study team.
Clinical Research Associate overseeing Phase I - IV clinical trials at IQVIA. Collaborating with site staff to ensure study compliance and data integrity while supporting global clients.
Clinical Research Associate conducting Phase I to IV clinical trials in Canada. Collaborating with clinical teams to ensure compliance and study execution.
Senior Clinical Research Associate executing and supervising clinical trials from Phase I to IV. Collaborating closely with clinical trial directors and assessing site capabilities in Canada.
Research Associate supporting DWIHN’s Innovation & Community Engagement team by conducting applied research and informing strategic decisions. Ensuring initiatives are grounded in evidence and reflective of trends and needs in behavioral health.
Research Analyst at Ipsos supporting strategic insights through research project execution. Involves quantitative research design and managing key market research projects.
Clinical Research Associate monitoring clinical studies in immunology and cardiovascular diseases at AstraZeneca. Ensuring accurate data submission and reporting in a collaborative team environment.
Research Analyst developing quantitative analyses on the Chinese energy market for clients. Enjoy autonomy and engagement opportunities in a supportive environment.
Research Specialist providing legal and business research support at Dentons Canada. Utilizing AI tools and collaborating in a hybrid environment across the firm.