Janice Bell Email and Phone Number

This role is responsible for coordinating the daily activities of designated clinical research trials, which includes recruitment, screening, data collection, and management of study related documents; assist in research related staff training; and assist in other assigned clinical and administrative tasks.Oversee the recruitment, screening, enrolling, and obtaining of consent from study participants. Recruitment includes using proper resources in identifying potential research participants, preparation of advertising materials, and coordinating advertising implementation.Oversee research participant visits throughout the study, this includes preparing paperwork, conducting study related procedures, completing case report forms and properly interacting with research director, study physicians, and co-investigators on participant progress. This also includes coordinating activities and education of other research staff/technicianBlood sample processing responsible for handling, processing, and analyzing blood samples to ensure accurate and timely results for diagnostic purposes. This role involves working in a laboratory setting, adhering to strict protocols to maintain sample integrity and comply with health and safety regulationsCentrifuge blood samples to separate components, such as plasma, serum, and cellsPrepare samples for various types of tests, including hematology, chemistry, and immunology assaysOversee all data entry into EDC Systems, quarterly meetings to discuss outcomes, worked directly with Dr. Fayad to assure data entry and quality

The Michigan Center for Translational Pathology (MCTP) was formed in 2007 as a focused initiative to bring basic research discoveries from molecular medicine to clinical applications for the identification of biomarkers and therapeutic targets for cancer diagnosis and treatment. We have made several noteworthy discoveries that have driven cancer research forward and intend to develop these findings to advance cancer diagnostics and targeted therapies. It is our hope to explore avenues for the development of personalized medicine based upon an individual’s specific genetic abnormalities underlying the development of his/her disease. MCTP’s overarching mission is to: 1) To establish the University of Michigan as the international leader in discovery and characterization of disease biomarkers and therapeutic targets using an integrated multi-disciplinary, systems biology approach. 2) Establish a new paradigm of bringing personalized medicine to routine clinical care through the use of high throughput sequencing. In parallel with the UM Health System, MCTP also has four core components to the mission: research, education, patient care and service. Our specific goals are to: Discover new disease biomarkers and candidate therapeutic targets using genomic, proteomic, and bioinformatics approaches. Employ a systems biology perspective in characterizing the molecular alterations in human disease. Translate and commercialize molecular discoveries for clinical utility. Train future translational cancer researchers. Ensure the long term scientific and funding success of the MCTP. Translate next generation sequencing based approaches (including associated bioinformatics) for clinical use in personalized medicine. Transform the practice of pathology and medicine.

•This role is responsible for coordinating the daily activities of designated clinical research trials, which includes recruitment, screening, data collection, and management of study related documents; assist in research related staff training; and assist in other assigned clinical and administrative appointed tasks.•Oversee the recruitment, screening, enrolling, and obtaining of consent from study participants. Recruitment includes using proper resources in identifying potential research participants, preparation of advertising materials, and coordinating advertising implementation.•Oversee research participant visits throughout the study, This includes preparing paperwork, conducting study related procedures, completing case report forms and properly interacting with research director, study physicians, and co-investigators on participant progress. This also includes coordinating activities and education of other research staff/technicians.•For multi-center trials, preparing paperwork, binders, and proper personnel for monitoring visits.•Monitor and detect all adverse outcomes and meet all requirements of the IRB and FDA for reporting and documentation. Assure program compliance with all federal, state, and local regulatory and institutional policies.•Scoring of study related procedures, including questionnaires, performance tests, and sleep related procedures. Also responsible for maintenance of study related database.•Involvement in outreach activities and external resources for research related purposes. This may include, but is not limited to, meeting with external physicians and their staff for recruitment or maintaining communication with a study sponsor.•Facilitate research participant questions and adverse events with proper research study staff.

• This role is responsible for coordinating the daily activities of designated clinical research trials, which includes recruitment, screening, data collection, and management of study related documents; assist in research related staff training; and assist in other assigned clinical and administrative appointed tasks.• Oversee the recruitment, screening, enrolling, and obtaining of consent from study participants. Recruitment includes using proper resources in identifying potential research participants, preparation of advertising materials, and coordinating advertising implementation.• Oversee research participant visits throughout the study, This includes preparing paperwork, conducting study related procedures, completing case report forms and properly interacting with research director, study physicians, and co-investigators on participant progress. This also includes coordinating activities and education of other research staff/technicians.• For multi-center trials, preparing paperwork, binders, and proper personnel for monitoring visits.• Monitor and detect all adverse outcomes and meet all requirements of the IRB and FDA for reporting and documentation. Assure program compliance with all federal, state, and local regulatory and institutional policies.• Scoring of study related procedures, including questionnaires, performance tests, and sleep related procedures. Also responsible for maintenance of study related database.• Involvement in outreach activities and external resources for research related purposes. This may include, but is not limited to, meeting with external physicians and their staff for recruitment or maintaining communication with a study sponsor.• Facilitate research participant questions and adverse events with proper research study staff.

• Implementation and execution of research study recruitment. These duties include discussion of recruitment strategies for a given study with the assigned Clinical Research Coordinator (CRC)and/or Principal Investigator. Responsible for identification of potential participants (whether database reviews, recruitment through external physician practices, advertising, etc.).• Responsible for making initial contact with potential research participants, describing the study to them, performing pre-screening questionnaires and possible scheduling screening visits. Continuously recruiting for all assigned studies and to implementing strategies as needed, under the direction of the Principal Investigator, CRC, or Director. Part of recruitment will also be responsibility of maintaining a recruitment database for participants screened for a particular study as well as maintenance of a general research database.• Responsible for the development of recruitment materials, which includes development of flyers, recruitment letters, coordination of media buys for recruitment, and maintenance of any related documentation.• Involvement in departmental responsibilities. • Responsible for monitoring and ordering of all needed office and clinical supplies for the Research Center.• Work on other projects and duties, including clinical or administrative directed projects, as assigned by Director of Research.• Phlebotomy on research patients

Together with its customers and sales partners, Allianz is one of the strongest financial communities with a presence in over 70 countries. Around 78 million private and corporate customers rely on Allianz's knowledge, global reach, capital strength and solidity to help them make the most of financial opportunities and to avoid and safeguard themselves against risks. Our ambition is to be the partner of choice - with excellent employees, top-notch operating performance and the necessary financial strengthKey ResponsibilitiesSupports our underwriters by performing a variety of essential functions and/or tasksincluding, but not limited to those identified below:•Process incoming inquiries and calls in an automated/non-automated call delivery equipment•Assume ownership of customer inquiries, concerns and feedback until the resolution is successfully accomplished and or resolved•Escalate difficult questions, issues and complaints to SR Account Representative or Account Specialist•Process all transactions in PI and or CL products including but, not limited to High Net Worth, HPR, Manuel Processing, Composite Rating, ISO Rating, PEN’s, and other cross functional and cross transactional skills•Compute rates and premiums for new and renewal business. Compute rates and premiums for new and renewal business•Perform applicable procedures in compliance with home office, corporate and regulatory standards•Gather, organize and analyze specified information and reports to assist in the underwriting decisions•Comply with all internal procedures and practices demonstrating the ability to meet service performance and quality standards•Complete assignments and achieve targeted results•Adjusts to plans changing priorities by supporting cross trained and cross functional teams and needed•Work effectively in a team environment using professional interpersonal and communication skills by applying the competencies and shared values in a timely manner-

Supervises the daily clinical research operations for the research program, fully integrating research protocols with applicable research management systems and processes. Responsible for supervising and coordinating the organization and execution of multiple research projects that may involve multiple sites of a specialized research program, fully integrated with applicable research management systems and processes, as well as management of the research team. Develops and maintains comprehensive knowledge of research program and associated protocols. Coordinates the comprehensive and compliant execution of protocols in accordance with research governing entity requirements, including but not limited to Sponsor, FDA and IRB requirements. Assists PI with research study design and development of research protocol. Responsible for research project budget development, identifying and classifying routine care versus research related care. Supervises research protocol requirements including; timely completion and communication of regulatory documents, reporting of serious adverse events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines. Serves as a liaison between investigators, research personnel, to assist in protocol interpretation, enrollment and safety questions. Supervises and coordinates research project budget development, assisting PI with identifying and classifying routine care versus research. May develop and coordinate the research subject study schedule and calendar in compliance with the research protocol. Supervises and coordinates the organization of research data for the research program.

CME Project Manager Position Overview:Under the supervision of the Neurological Institute CME Manager, the Neurological Institute CME Project Manager develops and administers CME symposia and other educational programs for the Neurological Institute. Seeks education grants from industry, completes CME applications and associated forms. Summary: Assists in the development of departmental projects. Manages implementation and maintenance of projects and process improvements. Coordinates resources, develops project plans and process flows.Job Responsibilities: Facilitates development, implementation and coordination of resources to complete projects and process improvement initiatives. Develops, implements and maintains project work plans. Designs process flows to support project scope. Prepares regular progress reports and distributes information. Collects and organizes project data results; analyzes results, interprets control charts and produces reports that evaluate results. May make recommendations for changes as requested. Facilitates meetings with project representatives. Adheres to timelines and organizational expectations. Resolves team conflicts. Partners with IT personnel to identify, evaluate and coordinate system enhancements designed to support project requirements. Performs other duties as assigned.

Plans educational activities for the Neurological Institute.

Serves as the Institute Research Regulatory Officer, responsible for developing, implementing, and maintaining the Research Regulatory & Quality Assurance (QA) Program for the Institute in collaboration with Institute and central research administration management. Serves as the Institute liaison with central compliance offices and leads all regulatory and quality audits and inspections, identifying and resolving compliance issues and concerns, developing and implementing quality improvement plans to mitigate future risk, and reporting on research compliance activities. Establishes standard operating procedures and guidelines for the conduct of research that are in alignment with those of the sponsoring organization, external regulatory agencies and central research administration offices. Develops and maintains research education program, tracking participation and certification.

Responsible for the coordination of the implementation and conduct of multiple research projects of a specialized research program, fully integrated with applicable research management systems and processes. Oversees the administrative functions of multi-site research studies. Develops and maintains comprehensive knowledge of research program and associated protocols. Coordinates the comprehensive and compliant execution of protocols in accordance with research governing entity requirements, including but not limited to Sponsor, FDA and IRB requirements. Administers and performs specialized testing as required by research protocol. Coordinates the development of training and educational material for research program and orients, educates and trains appropriate personnel and research subjects. Assists PI with research study design and development of research protocol. Responsible for research project budget development, identifying and classifying routine care vs research related care.

Responsible for the coordination of the implementation and conduct of multiple research projects of a specialized research program, fully integrated with applicable research management systems and processes. Oversees the administrative functions of multi-site research studies. Develops and maintains comprehensive knowledge of research program and associated protocols. Coordinates the comprehensive and compliant execution of protocols in accordance with research governing entity requirements, including but not limited to Sponsor, FDA and IRB requirements. Administers and performs specialized testing as required by research protocol. Coordinates the development of training and educational material for research program and orients, educates and trains appropriate personnel and research subjects. Assists PI with research study design and development of research protocol. Responsible for research project budget development, identifying and classifying routine care vs research related care.