Washington University in St. Louis
Senior Clinical Research Coordinator - Psychiatry
Washington University in St. Louis, St Louis, Missouri, United States
Senior Clinical Research Coordinator
The Cruchaga lab at the NeuroGenomics and Informatics Center is hiring a senior clinical research coordinator. This person will oversee and coordinate complex or multi-site clinical research studies, serve as a resource to provide comprehensive information to clinical research staff, promote smooth clinical operations, prepare regulatory compliance documents, coordinate interaction with other departments, and supervise clinical research coordinators and staff. Primary duties and responsibilities include: Acting as the primary liaison to the principal investigator in developing plans for clinical research projects; collaborating in the preparation of manuscripts for publication and preparation of grant proposals to sponsoring agencies; assisting in the preparation of amendments to protocols and/or modifications to study design as appropriate. Evaluating and interpreting collected clinical data in conjunction with the principal investigator as appropriate; preparing oral or written presentations or reports and analyses setting forth progress trends and providing recommendations or conclusions of the same. Managing protocol study start up and study launch, submission, and maintenance of essential regulatory documents. Designing, implementing and managing all phases of study/protocol; ensuring compliance with protocol guidelines and requirements of regulatory agencies; identifying problems and/or inconsistencies and monitoring participants progress to include documentation and reporting of adverse events; resolving IRB/protocol management issues and recommending corrective action as appropriate; serving as liaison with funding or sponsoring agency. Responsible for the development of forms, questionnaires and the application of research techniques; assisting in writing instructional procedure manuals for study progress, data collection and coding. Assisting in budget review and invoice tracking. Providing guidance and supervision to members of research team in the implementation and evaluation of clinical research; training new staff; serve as lead or as point of reference for other research coordinators for questions, staff scheduling, feedback on performance. Participate in the hiring, training, and evaluation of clinical research staff. Assisting in scheduling and facilitating site visits by external and internal monitors and auditors. Providing study coordinator functions and performing all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consenting participants for non-therapeutic clinical trials and performing blood draws and other specimen collection as needed. Performing other duties incidental to the work described above. Required qualifications: Education: Bachelors degree or combination of education and/or experience may substitute for minimum education. Certifications: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross. Work experience: Clinical research (3 years). Skills: Supervision. A driver's license is not required for this position.
The Cruchaga lab at the NeuroGenomics and Informatics Center is hiring a senior clinical research coordinator. This person will oversee and coordinate complex or multi-site clinical research studies, serve as a resource to provide comprehensive information to clinical research staff, promote smooth clinical operations, prepare regulatory compliance documents, coordinate interaction with other departments, and supervise clinical research coordinators and staff. Primary duties and responsibilities include: Acting as the primary liaison to the principal investigator in developing plans for clinical research projects; collaborating in the preparation of manuscripts for publication and preparation of grant proposals to sponsoring agencies; assisting in the preparation of amendments to protocols and/or modifications to study design as appropriate. Evaluating and interpreting collected clinical data in conjunction with the principal investigator as appropriate; preparing oral or written presentations or reports and analyses setting forth progress trends and providing recommendations or conclusions of the same. Managing protocol study start up and study launch, submission, and maintenance of essential regulatory documents. Designing, implementing and managing all phases of study/protocol; ensuring compliance with protocol guidelines and requirements of regulatory agencies; identifying problems and/or inconsistencies and monitoring participants progress to include documentation and reporting of adverse events; resolving IRB/protocol management issues and recommending corrective action as appropriate; serving as liaison with funding or sponsoring agency. Responsible for the development of forms, questionnaires and the application of research techniques; assisting in writing instructional procedure manuals for study progress, data collection and coding. Assisting in budget review and invoice tracking. Providing guidance and supervision to members of research team in the implementation and evaluation of clinical research; training new staff; serve as lead or as point of reference for other research coordinators for questions, staff scheduling, feedback on performance. Participate in the hiring, training, and evaluation of clinical research staff. Assisting in scheduling and facilitating site visits by external and internal monitors and auditors. Providing study coordinator functions and performing all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consenting participants for non-therapeutic clinical trials and performing blood draws and other specimen collection as needed. Performing other duties incidental to the work described above. Required qualifications: Education: Bachelors degree or combination of education and/or experience may substitute for minimum education. Certifications: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross. Work experience: Clinical research (3 years). Skills: Supervision. A driver's license is not required for this position.