Job Title
Principal Clinical Research Scientist
Job Profile
Principal Clinical Research Scientist','130000060U','!*!Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 70,000 people.
Primary Job Function
Provides scientific expertise throughout the development and implementation of clinical studies. Writes/manages clinical trial protocols, protocol amendments, and scientific publications. Works on cross-functional teams and interacts with various study support groups in order to assist in clinical strategy, the development of study plans, and project deliverables.
Uses their scientific knowledge in order to provide directives to staff as well as study sites.
Core Job Responsibilities
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
· Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
· Communicates with R&D;, Regulatory Affairs, Senior Management and investigational sites on clinical trial work and clinical science objectives through cross-functional meetings and/or presentations.
· Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process.
· Participates in the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction.
· Writes study protocols, protocol amendments, informed consents, clinical trial training material and scientific papers for publication by evaluating scientific literature and publications, analyzing scientific data and staying abreast of current clinical practice. Responsible for providing the clinical science support on cross-functional teams and advising on scientific aspects of the clinical trials.
· Interprets clinical study results in preparation for new product applications by evaluating scientific literature and publications, analyzing scientific data and staying abreast of current clinical practice.
· Presents scientific data by communicating accurate, succinct summaries of clinical study work at industry gatherings, investigational meetings and regulatory agency meetings.
· Provides accurate progress reports on clinical projects by writing assigned clinical portions of reports for submission to regulatory agencies, Institutional Review Boards, Medical Ethics Committees, etc
Position Accountability / Scope
Understands business environment and relates extensive knowledge of internal and external technological activities to trends. Interfaces with senior management on significant matters, often requiring the coordination of activity across organizational units. Participates in the development of other technical contributors by facilitating training and providing feedback and guidance. May lead a project team. Provides technical leadership to business units. Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees. Exercises judgment independently. Plans and organizes project assignments of substantial variety and complexity. Erroneous decisions or recommendations would typically result in failure to achieve major organizational objectives.','!*!Minimum Education
Advanced degree (MD, PhD, or PharmD degree) highly preferred for consideration. Bachelors degree required. Degree in the sciences, medicine, or similar discipline highly preferred. Minimum of 8 years of related work experience with a complete understanding of specified functional area, or an equivalent combination of education and work experience.
Minimum Experience / Training Required
Comprehensive knowledge of a particular technological field. Experience in coronary and endovascular technological field highly preferred. Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships. Is recognized as an expert in work group and across functions. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Has broad knowledge of various technical alternatives and their potential impact on the business.','Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)','Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)','Experienced','CLINICAL RESEARCH','USA-California-Santa Clara','','AVD-Vascular','Full-time','Day','Day','Yes, 15 % of the Time','','','Principal Clinical Research Scientist
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Location: USA-CA-Santa Clara |
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Posted on
Aug 16,2026 |
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Company info
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