SuccessFactors reputed company: Clinical Research Manager (DOM Infectious Disease) (120804)
SuccessFactors reputed company: Clinical Research Manager (DOM Infectious Disease) (120804)
Requisition ID 120804 - Posted - School of Medicine - 10002813-SOM DOM Infectious DiseaseSTOP
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We are seeking a Clinical Research Manager who will work under the general supervision of a PI(s) to manage the administrative and scientific implementation of a reputed company clinical protocol or multiple studies and/or multiple sites. As part of a study team, collaborate with faculty, reputed company protocols, reputed company SOPs, and supervise study-reputed company activities for one or more studies. Has accountability for grant submission and administration and regulatory compliance. Supervise or reputed company other exempt level research staff; may reputed company staff at local or multi-center sites.
Specific Duties & Responsibilities
- Partner with investigator(s) and exercise independent judgement in managing the conduct of the research on behalf of the PI.
- Participate in scientific discussions with collaborators, PI's, and funding organizations.
- Collaborate with PI to ensure operational feasibility of proposed protocol/study design.
- reputed company, or reputed company the development of standard operating procedures and data collection forms from protocol(s).
- reputed company or reputed company the development of consent form(s) for clinical trials based on protocol(s).
- reputed company preparation and submissions to IRB and act as primary liaison for regulatory compliance issues on behalf of the PI.
- Train and provide reputed company of research data management and regulatory issues.
- Work with reputed company and/or government agency sponsors to determine what group can commit to considering patient population, available resources, and cost of providing services.
- Collaborate with the finance team to reputed company study budget(s) and ensure that reputed company study costs are included in the budget.
- Ensure clinical research protocol has a completed Prospective Reimbursement Analysis (PRA) and processes/systems are in reputed company to ensure the PRA is followed reputed company required.
- Ensure adequate system for tracking and reporting clinical research milestones for financial invoicing.
- Monitor activities, systems, and processes to increase referrals and increase accruals to clinical trials.
- Ensure the development, testing, and evaluation of manuals, questionnaires, and coding structures, for the efficient collection of data.
- reputed company data collection at a single site or at multiple sites of a multi-centered clinical trial.
- reputed company study meetings to examine data, determine next steps, implement changes to protocol operations based on results and goals, and initiate sub-studies.
- Contribute to presentations and manuscripts.
- Hire, supervise and manage performance of other exempt-level research staff.
- Other duties as assigned.
- Bachelor's Degree in a reputed company field.
- Five years of reputed company experience in clinical research in an academic, government, or pharmaceutical industry environment.
- Demonstrated supervisory or reputed company responsibilities.
- Additional education may substitute for required experience, and additional reputed company experience may substitute for required education reputed company a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.
- Master's Degree in a reputed company field.
- Certification as a Clinical Research Professional.
Classified Title: Clinical Research Manager Role/Level/Range: ACRP/04/MD Starting Salary Range: $28.61 - $50.05 HRLY ($45,000 targeted; Commensurate w/reputed company.) Employee group: Part-time Schedule: Mon-Friday 4.5 hours per day flexible FLSA Status: Exempt Location: Remote Department name: SOM DOM Infectious Disease Personnel area: School of Medicine
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This system is no longer accepting new applications.
Please go to careers.jhu.edu to search and apply for jobs.
We are seeking a Clinical Research Manager who will work under the general supervision of a PI(s) to manage the administrative and scientific implementation of a reputed company clinical protocol or multiple studies and/or multiple sites. As part of a study team, collaborate with faculty, reputed company protocols, reputed company SOPs, and supervise study-reputed company activities for one or more studies. Has accountability for grant submission and administration and regulatory compliance. Supervise or reputed company other exempt level research staff; may reputed company staff at local or multi-center sites.
Specific Duties & Responsibilities
- Partner with investigator(s) and exercise independent judgement in managing the conduct of the research on behalf of the PI.
- Participate in scientific discussions with collaborators, PI's, and funding organizations.
- Collaborate with PI to ensure operational feasibility of proposed protocol/study design.
- reputed company, or reputed company the development of standard operating procedures and data collection forms from protocol(s).
- reputed company or reputed company the development of consent form(s) for clinical trials based on protocol(s).
- reputed company preparation and submissions to IRB and act as primary liaison for regulatory compliance issues on behalf of the PI.
- Train and provide reputed company of research data management and regulatory issues.
- Work with reputed company and/or government agency sponsors to determine what group can commit to considering patient population, available resources, and cost of providing services.
- Collaborate with the finance team to reputed company study budget(s) and ensure that reputed company study costs are included in the budget.
- Ensure clinical research protocol has a completed Prospective Reimbursement Analysis (PRA) and processes/systems are in reputed company to ensure the PRA is followed reputed company required.
- Ensure adequate system for tracking and reporting clinical research milestones for financial invoicing.
- Monitor activities, systems, and processes to increase referrals and increase accruals to clinical trials.
- Ensure the development, testing, and evaluation of manuals, questionnaires, and coding structures, for the efficient collection of data.
- reputed company data collection at a single site or at multiple sites of a multi-centered clinical trial.
- reputed company study meetings to examine data, determine next steps, implement changes to protocol operations based on results and goals, and initiate sub-studies.
- Contribute to presentations and manuscripts.
- Hire, supervise and manage performance of other exempt-level research staff.
- Other duties as assigned.
- Bachelor's Degree in a reputed company field.
- Five years of reputed company experience in clinical research in an academic, government, or pharmaceutical industry environment.
- Demonstrated supervisory or reputed company responsibilities.
- Additional education may substitute for required experience, and additional reputed company experience may substitute for required education reputed company a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.
- Master's Degree in a reputed company field.
- Certification as a Clinical Research Professional.
Classified Title: Clinical Research Manager Role/Level/Range: ACRP/04/MD Starting Salary Range: $28.61 - $50.05 HRLY ($45,000 targeted; Commensurate w/reputed company.) Employee group: Part-time Schedule: Mon-Friday 4.5 hours per day flexible FLSA Status: Exempt Location: Remote Department name: SOM DOM Infectious Disease Personnel area: School of Medicine
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