The Clinical Scientist at Cook Research is responsible for providing senior leadership and scientific expertise. In addition, the Clinical Scientist will coordinate with cross-functional teams in the development of strategy and oversight for the clinical study/program.
Responsibilities
Develop and maintain relationships with physician experts (such as National Principal Investigators, Steering Committee Members) to meet company objectives for the project
Coordinate the presentation of information to DSMB, in accordance with the DSMB Charter, including, but not limited to, data summaries and presentations, study notifications, patient summaries, and attendance at meetings when necessary
Provide technical and scientific support/guidance for a specific project or area of treatment/technology or disease
Work with cross functional teams (Engineering, Regulatory, Business Units, etc.) to evaluate new clinical projects and study strategy
Develop clinical study designs and facilitate the transition of the project to clinical project management team
Review and provide input to clinical study-related documents, plans and training materials (e.g., CIP, IB, CRF Specifications, Study-specific IC Template, Clinical Study Overview Presentation, Progress Report)
Provide support and review materials for Investigator Meetings and Site Initiation Meetings
Lead efforts for the analysis, interpretation, presentation and reporting of clinical and imaging data to relevant stakeholders (project teams, executive management, physicians); collaborate with the CPM
In studies with an imaging component: Coordinate plan for receipt and review of imaging and coordinate efforts in the selection, training and management of core laboratory for independent review of imaging, as applicable
Work with relevant stakeholders to develop and execute publication and presentation plan for the study
Review study data and milestones, and coordinate study strategy with relevant stakeholders; and
Maintain effective communication with cross functional teams and stakeholders.
Qualifications
Advanced degree in Life Sciences or Engineering required, PhD or MD preferred
Extensive experience in the conduct and management of clinical studies
Working knowledge of the regulatory authorities and other regulatory requirements that may impact global clinical studies
Conscientious, influential person with an outstanding work ethic and strong personal discipline
Sufficiently assertive to deal with confrontational situations while recognizing the need to communicate in an effective and diplomatic manner
Ability to present a professional and personable demeanor in all interactions
Experience in writing study protocols and other technical documents
Qualified candidates must be legally authorized to be employed in the United States. Cook does not intend to provide sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Physical Requirements
Willingness and ability to travel 10-20% of the time
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Medical Equipment Manufacturing
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