Manager- Clinical Research Operations

Northside Hospital Research Position

Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond. Discover all the possibilities of a career at Northside today.

Primary Duties And Responsibilities

• Manage research projects assigned by the Research Program Director
• Manage assigned departments/staff
• Support Research Program with the development of appropriate goals, metrics and required documentation of project activities.
• Identify collaborative opportunities across project teams, practices, and hospital departments.
• Coordinate and lead meetings with NSH departments analyzing the feasibility of new research projects.
• Ensure the quality and integrity of research.
• Serve as a point of contact for Monitor visits from CROs, SMOs, and sponsors to help coordinate the visits with CRCs and CRNs and the availability of all necessary information to ensure accuracy and compliance.
• Monitors all research activity and maintains awareness of all clinical research projects.
• Provides compliance oversight for day-to-day operations
• Develops, maintains, and evaluates the SOPs for administering clinical research
• Conducts training on GCP, FDA, NIH, Human Subject Protection and necessary regulations.

Additional Duties And Responsibilities

• Resolve research conflicts during the normal course of business
• Maintain professional knowledge and skills, particularly in the areas of Good Clinical Practice guidelines and other research regulations
• Participate in the review, development and maintenance of automated processes and information technology for clinical research related activities
• Develop, maintain, and deliver education and training programs for the NSH research community, protection of human subjects, the research life cycle, protocol development, monitoring visits, and others.
• Other duties as assigned

Qualifications

Bachelor's degree in a relevant field. MBA preferred.

Minimum of 5 years' experience in a clinical research setting

Ability to correctly interpret laws, regulations and policies related to research compliance

Excellent organizational and project management skills with the ability to manage multiple tasks simultaneously

Knowledge of clinical trial policies and regulations and Good Clinical Practice (GCP)

Established interpersonal skills combined with the ability to be highly motivated and work independently

Demonstrated analytical and problem solving skills

Ability to work independently and as part of a team

Ability to manage teams of varying sizes

Knowledge of information technology systems supporting regulatory affairs, IRB and compliance research administration

Work Hours:

8-5p