Irb Manager Jobs in Alabama (NOW HIRING)

Management of Redcap database ... Assists the PI in the conduct of the clinical study according to FDS/IRB regulations and guidelines.

The role includes assisting with IRB submissions, maintaining regulatory documentation, and ... Ability to manage multiple priorities and regulatory submission deadlines. Collaborative and ...

Manages single IRB processes for multi-site studies and serves as primary liaison with relying institutions. 3. Ensures compliance with federal, state, and institutional regulations, including NIH ...

Prepare and manage documents required to initiate investigational drugs trials. Prepares research protocols for IRB submission, submits protocol amendments, prepares renewals and necessary regulatory ...

... IRB regulations, and Good Clinical Practice (GCP). * To assist with the management of the life ... cycle of the clinical trial as needed from study start-up through trial maintenance to study ...

... IRB submission processes. * Must have strong project management and risk assessment skills. * Must be able to communicate effectively with staff, investigators, sponsor representatives, legal ...

... and IRB submission processes. * Must have good project management and risk assessment skills. * Must be able to communicate effectively with staff, investigators, sponsor representatives, legal ...

... IRB regulations, and Good Clinical Practice (GCP). * To assist with the management of the life ... cycle of the clinical trial as needed from study start-up through trial maintenance to study ...

Coordinates and manages clinical care activities for pediatric hematology/oncology patients ... Ensures compliance with federal regulations, IRB requirements, sponsor guidelines, and Good ...

This role manages major compliance areas-including IRB, IACUC, biosafety/biosecurity, responsible conduct of research, export controls, material/data transfer agreements, and time & effort reporting.

Coordinates and manages clinical care activities for pediatric hematology/oncology patients ... Ensures compliance with federal regulations, IRB requirements, sponsor guidelines, and Good ...

IRB submissions, educational materials, reports, grant renewal reports, and study forms). * To ... Have strong project management and risk assessment skills. * Be able to communicate effectively ...

Prepares Institutional Research Board (IRB) documents under the direction of the PI, assists with ... Manages own time effectively and prioritizes work to achieve maximum results in a timely manner.

Develops or provides input for IRB documents. * Manages the life cycle of clinical research studies from feasibility to start-up through maintenance to closure. Manages participant care, including ...

Develops or provides input for IRB documents. * Manages the life cycle of clinical research studies from feasibility to start-up through maintenance to closure. * Manages participant care, including ...

... management. * Assists Research Protections staff and HMRI administration, as needed, with pre-clinical and clinical research areas of need, including Research Credentialing, IRB, Institutional Care ...

... IRB) requirements, Good Clinical Practice (GCP), HIPAA, and all applicable regulatory standards. * Manages clinical research activities throughout the study lifecycle, including participant ...

Ensure compliance with IRB protocols, HIPAA regulations, and institutional policies. * Assist with ... Ability to work independently and manage time-sensitive tasks * High level of professionalism ...

Manages all aspects of assigned clinical studies, including education. * Collects, analyzes, and ... Knowledge of IRB processes and HIPAA regulations. * Strong attention to detail for accurate data ...

Conducts and understands all study activities in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP). * Manages the life cycle of the clinical trial from study start-up ...