Sr Clinical Research Program Manager
About The Position
SUMMARY: Reporting to the Principal Investigator(s), and in accordance with established policies and procedures, the incumbent is responsible for the operation of research programs, including recruitment, implementation programs, processes and outcome evaluation of the program. color:blue Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: Brown University Health employees are expected to embrace Brown University Health's mission of Delivering health with care and successfully role model Brown University Health's values of Compassion, Accountability, Respect, and Excellence as these guide our everyday actions with patients, customers and one another. Assists Principal Investigator(s) with development, design and data management specifics of new studies and forms; may assist with tabulating and reviewing data results for publication and reporting. Also assists in developing grant applications, developing and managing budgets, subcontracts, and expenditures. Provides for training and orientation to research and grant procedures. Coordinates work schedule, monitors adherence to procedures/protocols. Provides input into development of performance evaluation for non-clinical aspects of staff assigned to project. Recommends corrective action as appropriate. May organize and implement aspects of research protocols and assist in coordinating clinical research projects, which may include: record review, establishing and maintaining research records, and entering data into computerized database. Assists research investigators in budgeting and managing financial accounts effectively within the guidelines and policies established by the Hospital as well as sponsoring agencies. Resolves problems and monitors monthly expense reports for accuracy and conformance to budget. Addresses variances as required to meet the grant budget. May prepare special analyses as appropriate. Coordinates all required submissions related to protocol, physicians and procedures to the protocol office – regulatory affairs. Coordinates collaborative work with other investigators and/or sites. Also coordinates audits and on-site visits by the pharmaceutical companies and any other appropriate groups. Maintains quality assurance, safety, environmental and infection control in accordance with established hospital department policies and objectives. Coordinates and/or conducts annual training in these areas. May require outside travel to evaluate sites or for other grant-related reasons. Maintains and enhances professional expertise through educational opportunities and review of pertinent literature.
Requirements
- Masters Degree in relevant discipline or occupation is preferred. May consider relevant education and/or work experience year for year for degree.
- Excellent computer skills and familiarity with statistics.
- May require valid driver’s license where grant requires travel outside of hospital.
- Three or more years progressively more responsible relevant experience, depending on size and complexity of program(s) or organization.
- Experience should demonstrate leadership skills and ability to effectively prepare and monitor budgets.
Responsibilities
- Assists Principal Investigator(s) with development, design and data management specifics of new studies and forms; may assist with tabulating and reviewing data results for publication and reporting.
- Assists in developing grant applications, developing and managing budgets, subcontracts, and expenditures.
- Provides for training and orientation to research and grant procedures.
- Coordinates work schedule, monitors adherence to procedures/protocols.
- Provides input into development of performance evaluation for non-clinical aspects of staff assigned to project.
- Recommends corrective action as appropriate.
- May organize and implement aspects of research protocols and assist in coordinating clinical research projects, which may include: record review, establishing and maintaining research records, and entering data into computerized database.
- Assists research investigators in budgeting and managing financial accounts effectively within the guidelines and policies established by the Hospital as well as sponsoring agencies.
- Resolves problems and monitors monthly expense reports for accuracy and conformance to budget.
- Addresses variances as required to meet the grant budget.
- May prepare special analyses as appropriate.
- Coordinates all required submissions related to protocol, physicians and procedures to the protocol office – regulatory affairs.
- Coordinates collaborative work with other investigators and/or sites.
- Also coordinates audits and on-site visits by the pharmaceutical companies and any other appropriate groups.
- Maintains quality assurance, safety, environmental and infection control in accordance with established hospital department policies and objectives.
- Coordinates and/or conducts annual training in these areas.
- May require outside travel to evaluate sites or for other grant-related reasons.
- Maintains and enhances professional expertise through educational opportunities and review of pertinent literature.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
Number of Employees
101-250 employees
