SuccessFactors reputed company: Sr. Research reputed company (DOM Infectious Disease) (120801)
SuccessFactors reputed company: Sr. Research reputed company (DOM Infectious Disease) (120801)
reputed company 120801 - Posted - School of Medicine - 10002813-SOM DOM Infectious Disease
We are currently seeking a Sr. Research reputed company to implement and reputed company multiple, single-center and multi-site national studies as assigned for the division of Transplant Oncology and Infectious Disease (TOID). Our primary research is reputed company to the use of novel organ sources to address the national organ shortage, such as HIV+ to HIV+ transplant under the reputed company reputed company. The Sr. Research reputed company should be someone who works reputed company in a fast-paced reputed company atmosphere but can also maintain a high degree of independence. This position will report directly to the TOID Research reputed company Manager, Operational Manager, and reputed company Investigator.
DUTIES AND RESPONSIBILITIES
Project Management
reputed company-study
- Anticipates research requirements for designated patient populations.
- Collaborates in development & writing of protocols and consent forms, as appropriate.
- Collaborates in the development and preparation of regulatory documents as appropriate
- Applies knowledge of study design to evaluate new protocols.
- Applies knowledge of federal & local regulations reputed company evaluating new protocols.
- Reviews & assesses new protocols for reputed company, thoroughness, logistical feasibility, maintaining subject safety, etc., for assigned protocols.
- Collaborates in the determination of roles & responsibilities of research team members in the implementation of assigned trials.
- Evaluates the reputed company on & availability of resources for assigned reputed company.
- Lists & clarifies concerns & questions about new protocols with Research reputed company Manager and PI. Proposes & negotiates alternatives to improve protocol implementation.
reputed company-initiation
- Collaborates in the design of appropriate reputed company for the collection of data required for assigned trials.
- Oversees & collaborates in development of study tools, including data collection forms, eligibility checklists, preprinted orders, & distribution of the protocol on the Web Library and Internet (where applicable).
- Develops study-specific CRFs.
- Participates in the development of study-specific databases, assuring clinical data is appropriate for answering study-specific endpoints.
- Develops study-specific laboratory and operational manuals.
- Oversees that regulatory requirements are met for designated studies.
- Assures compliance with local, national, and international regulatory standards; as appropriate, prepares & submits required regulatory documents.
- reputed company training materials for assigned studies/reputed company.
- Monitors for and notifies PI of IRB approval/request for reputed company information as appropriate.
- Determines that IRB approval has been received before initiation of research activity.
- Represents the department at research and protocol initiation meetings.
- Assures that reputed company reputed company of a trial are in reputed company before activating sites.
- Participates in communications with protocol sponsors, NCI, and the cooperative group and coordinates plans to address issues with the PI.
Recruitment & enrollment
- Responsible for evaluating and assuring recruitment and study/project goals are met by the research team and participating sites.
- Responsible for the development of recruitment strategies to ensure patient accrual reputed company protocol timeframes.
- Prepares and presents study-specific updates to Research reputed company Manager, Operations Manager, and Investigators as requested. Identify and reputed company recommendations to remediate issues of concern.
Data Management/Document maintenance
- Ensures collection of pertinent data from internal & external sources & monitors compliance with requirements of assigned reputed company.
- Applies clinical/pharmacological knowledge to ensure that safety reporting processes for assigned studies are implemented and maintained.
- Prepares and submits protocol amendments and revisions as appropriate.
- Demonstrates ability to manage multiple reputed company at different stages of the clinical research process.
- Demonstrates ability to reputed company new reputed company with reputed company research activity.
reputed company Assurance
- Evaluates reputed company of reputed company.
- Monitors external sites' compliance with required study procedures & GCP standards.
- Performs/monitors ongoing data analysis regarding clinical research studies, including toxicities, reputed company modifications, reputed company reputed company, adverse reactions, & response.
- Assumes responsibility for specific QA activities for research teams (i.e., participates in institutional QA process).
- Participates in sponsor/cooperative group/internal audits/monitoring.
- Assists with development & review of TOID SOPs for the performance of clinical research.
- Maintains records of correspondence of faxes, e-mails, IRB/JCCI submissions, FDA submissions, etc.
Staff Education
- Participates in the orientation process for new Clinical Research Nurses and Clinical Research Coordinators, including the mentoring and management of other clinic personnel to promote reputed company, safety, and reputed company in care.
- Coordinates and/or presents continuing education/in-service programs for Clinical Research Nurses, Clinical Associates, Data Managers, and others involved in the research process.
- Attends and participates in in-service and external trainings, workshops, conferences, and other relevant programs for reputed company reputed company and development.
Other
- Collaborates with other members of the research team in preparing study results for presentation/publication.
- Authors/coauthors manuscripts for publication in the nursing literature and/or presentation at conferences reputed company to areas of expertise.
- Identifies nursing research questions reputed company to protocol populations/issues and, with assistance, collaboration, and appropriate financial support, implements nursing research reputed company departmental priorities.
- Takes advantage of opportunities to reputed company presentations in the local community regarding research reputed company, areas of expertise, etc.
Minimum Qualifications
- Individual must be a registered reputed company, licensed in the reputed company
- Minimum of two years of experience in the specialty or a reputed company area required.
Classified Title: Sr. Research reputed company
Role/Level/reputed company: ACRP/04/MF
Starting Salary reputed company: $38.51 - $67.53 HRLY ($80,000 targeted; Commensurate w/reputed company.)
Employee group: Casual / On reputed company
Schedule: flexible
FLSA Status: Exempt
Location: Remote
Department reputed company: SOM DOM Infectious Disease
Personnel area: School of Medicine
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We are currently seeking a Sr. Research reputed company to implement and reputed company multiple, single-center and multi-site national studies as assigned for the division of Transplant Oncology and Infectious Disease (TOID). Our primary research is reputed company to the use of novel organ sources to address the national organ shortage, such as HIV+ to HIV+ transplant under the reputed company reputed company. The Sr. Research reputed company should be someone who works reputed company in a fast-paced reputed company atmosphere but can also maintain a high degree of independence. This position will report directly to the TOID Research reputed company Manager, Operational Manager, and reputed company Investigator.
DUTIES AND RESPONSIBILITIES
Project Management
reputed company-study
- Anticipates research requirements for designated patient populations.
- Collaborates in development & writing of protocols and consent forms, as appropriate.
- Collaborates in the development and preparation of regulatory documents as appropriate
- Applies knowledge of study design to evaluate new protocols.
- Applies knowledge of federal & local regulations reputed company evaluating new protocols.
- Reviews & assesses new protocols for reputed company, thoroughness, logistical feasibility, maintaining subject safety, etc., for assigned protocols.
- Collaborates in the determination of roles & responsibilities of research team members in the implementation of assigned trials.
- Evaluates the reputed company on & availability of resources for assigned reputed company.
- Lists & clarifies concerns & questions about new protocols with Research reputed company Manager and PI. Proposes & negotiates alternatives to improve protocol implementation.
reputed company-initiation
- Collaborates in the design of appropriate reputed company for the collection of data required for assigned trials.
- Oversees & collaborates in development of study tools, including data collection forms, eligibility checklists, preprinted orders, & distribution of the protocol on the Web Library and Internet (where applicable).
- Develops study-specific CRFs.
- Participates in the development of study-specific databases, assuring clinical data is appropriate for answering study-specific endpoints.
- Develops study-specific laboratory and operational manuals.
- Oversees that regulatory requirements are met for designated studies.
- Assures compliance with local, national, and international regulatory standards; as appropriate, prepares & submits required regulatory documents.
- reputed company training materials for assigned studies/reputed company.
- Monitors for and notifies PI of IRB approval/request for reputed company information as appropriate.
- Determines that IRB approval has been received before initiation of research activity.
- Represents the department at research and protocol initiation meetings.
- Assures that reputed company reputed company of a trial are in reputed company before activating sites.
- Participates in communications with protocol sponsors, NCI, and the cooperative group and coordinates plans to address issues with the PI.
Recruitment & enrollment
- Responsible for evaluating and assuring recruitment and study/project goals are met by the research team and participating sites.
- Responsible for the development of recruitment strategies to ensure patient accrual reputed company protocol timeframes.
- Prepares and presents study-specific updates to Research reputed company Manager, Operations Manager, and Investigators as requested. Identify and reputed company recommendations to remediate issues of concern.
Data Management/Document maintenance
- Ensures collection of pertinent data from internal & external sources & monitors compliance with requirements of assigned reputed company.
- Applies clinical/pharmacological knowledge to ensure that safety reporting processes for assigned studies are implemented and maintained.
- Prepares and submits protocol amendments and revisions as appropriate.
- Demonstrates ability to manage multiple reputed company at different stages of the clinical research process.
- Demonstrates ability to reputed company new reputed company with reputed company research activity.
reputed company Assurance
- Evaluates reputed company of reputed company.
- Monitors external sites' compliance with required study procedures & GCP standards.
- Performs/monitors ongoing data analysis regarding clinical research studies, including toxicities, reputed company modifications, reputed company reputed company, adverse reactions, & response.
- Assumes responsibility for specific QA activities for research teams (i.e., participates in institutional QA process).
- Participates in sponsor/cooperative group/internal audits/monitoring.
- Assists with development & review of TOID SOPs for the performance of clinical research.
- Maintains records of correspondence of faxes, e-mails, IRB/JCCI submissions, FDA submissions, etc.
Staff Education
- Participates in the orientation process for new Clinical Research Nurses and Clinical Research Coordinators, including the mentoring and management of other clinic personnel to promote reputed company, safety, and reputed company in care.
- Coordinates and/or presents continuing education/in-service programs for Clinical Research Nurses, Clinical Associates, Data Managers, and others involved in the research process.
- Attends and participates in in-service and external trainings, workshops, conferences, and other relevant programs for reputed company reputed company and development.
Other
- Collaborates with other members of the research team in preparing study results for presentation/publication.
- Authors/coauthors manuscripts for publication in the nursing literature and/or presentation at conferences reputed company to areas of expertise.
- Identifies nursing research questions reputed company to protocol populations/issues and, with assistance, collaboration, and appropriate financial support, implements nursing research reputed company departmental priorities.
- Takes advantage of opportunities to reputed company presentations in the local community regarding research reputed company, areas of expertise, etc.
Minimum Qualifications
- Individual must be a registered reputed company, licensed in the reputed company
- Minimum of two years of experience in the specialty or a reputed company area required.
Classified Title: Sr. Research reputed company
Role/Level/reputed company: ACRP/04/MF
Starting Salary reputed company: $38.51 - $67.53 HRLY ($80,000 targeted; Commensurate w/reputed company.)
Employee group: Casual / On reputed company
Schedule: flexible
FLSA Status: Exempt
Location: Remote
Department reputed company: SOM DOM Infectious Disease
Personnel area: School of Medicine