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- Completes grant writing and submissions and oversees study protocol development and implementation within all departments and institutes within MHS including the negotiation of all research related contracts with external organizations, funders and pharmaceutical companies; coordinates review of contracts and legal agreements for OHR.
- Oversees all clinical research databases. Provides compliance and data management oversight and completes routine reporting to local and federal agencies and develops coverage analysis for budgets and ensures billing compliance.
- May take oversight responsibility of the Medical Research Office providing supervision, guidance and decision-making in absence of the Chief Medical Research Officer.
- Assists is overseeing OHR s daily activities, developing and implementing study protocol development and operational plans and ensuring that standard operating procedures are carried out in accordance with all federal and local standard operating procedures and ethical guidelines.
- Oversees study protocol development and implementation within all departments and institutes within MHS. Liaison with local and central Institutional Review Boards, Human Resources, and Grants Administration.
- Develops specific research departmental goals, standards, and objectives which directly support the strategic plan and vision of the organization.
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Research Operations Director - Hollywood, United States - Memorial Healthcare System
Description
Summary:
Under the direction of the Chief Medical Research Officer, supports the overall research mission of the department, by working to increase grant funding (and maintain existing funding), facilitate the successful implementation and maintenance of ongoing research activities, enhance department-wide efficiencies, and promote an informed and collaborative work environment for faculty and staff. Manages the daily operations of the clinical research department to ensure alignment with departmental and organizational objectives.
Responsibilities:
Education and Certification Requirements: Doctorate (Required) or Masters with at least ten (10) years in research, biology, chemistry, physical sciences, social sciences, public health, health sciences, math, statistics or related field of study.
Required Work Experience: Seven (7) years of experience in clinical research, that includes experience with research personnel management and research-related legal contracts.
