SuccessFactors reputed company: Clinical Research Manager (DOM Infectious Disease) (120804)
SuccessFactors reputed company: Clinical Research Manager (DOM Infectious Disease) (120804)
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 reputed company, 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 reputed company operating procedures and data collection forms from protocol(s).
- reputed company or reputed company the development of consent reputed company(s) for reputed company based on protocol(s).
- reputed company preparation and submissions to IRB and reputed company as primary reputed company for regulatory compliance issues on behalf of the PI.
- Train and reputed company reputed company of research data management and regulatory issues.
- Work with reputed company and/or government agency sponsors to determine what group can reputed company 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 reputed company.
- 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.
Minimum Qualifications
- Bachelor's Degree in a reputed company field.
- Five years of reputed company experience in clinical research in an reputed company, 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.
Preferred Qualifications
- Master's Degree in a reputed company field.
- Certification as a Clinical Research reputed company.
Classified Title: Clinical Research Manager
Role/Level/reputed company: ACRP/04/MD
Starting Salary reputed company: $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 reputed company: SOM DOM Infectious Disease
Personnel area: School of Medicine
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 reputed company, 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 reputed company operating procedures and data collection forms from protocol(s).
- reputed company or reputed company the development of consent reputed company(s) for reputed company based on protocol(s).
- reputed company preparation and submissions to IRB and reputed company as primary reputed company for regulatory compliance issues on behalf of the PI.
- Train and reputed company reputed company of research data management and regulatory issues.
- Work with reputed company and/or government agency sponsors to determine what group can reputed company 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 reputed company.
- 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.
Minimum Qualifications
- Bachelor's Degree in a reputed company field.
- Five years of reputed company experience in clinical research in an reputed company, 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.
Preferred Qualifications
- Master's Degree in a reputed company field.
- Certification as a Clinical Research reputed company.
Classified Title: Clinical Research Manager
Role/Level/reputed company: ACRP/04/MD
Starting Salary reputed company: $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 reputed company: SOM DOM Infectious Disease
Personnel area: School of Medicine