Principal Clinical Scientist at Abbott

Maple Grove, Minnesota, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Medical DevicesIndustries

Requirements

Advanced degree in the sciences, medicine, or similar discipline
8+ years of related work experience with a solid understanding of specified functional area, or an equivalent combination of education and work experience
Demonstrated ability to execute job responsibilities within corporate policies and standard operating procedures (inferred from job context)

Responsibilities

Develops, writes, or mentors others in creation of clinical strategy, risk management, or clinical evaluation planning for products and process changes, to gain regulatory approval for product release, additional claims or indications, by addressing issues from a clinical, medical, and scientific perspective and by interacting with appropriate personnel
Develops, writes, or mentors others in generation of study-related documents and/or contribute content and oversight of such documents, including, but not limited to, clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms
Designs or mentors others in the design of clinical trials and studies in collaboration with internal stakeholders including clinical project management, clinical operations, biostatistics data management, regulatory affairs, medical affairs as well as external stakeholders including steering and publication committees
Develop the scientific podium and publication strategy in close collaboration with cross-functional teams and lead the execution of the publication strategy through coordination with investigator authors and internal teams
Serve as an active member of study teams and provide scientific support to justify trial design and ongoing scientific analysis during protocol development. May include generation of pre-protocol documentation of scientific information
Review and critically analyze statistical analysis plans
Generate documents to support regulatory submissions for Abbott products and/or respond to questions from regulatory authorities about existing submissions
Work closely with the clinical study team including project management, biostatistician, data management, and other clinical study personnel
Significant interaction with leadership and regulatory authorities

Skills

Clinical Research

Clinical Trials

Project Management

Biostatistics

Data Management

Regulatory Affairs

Medical Devices

Abbott

Healthcare solutions in diagnostics and devices

About Abbott

Abbott Laboratories focuses on improving health through various medical technologies and health solutions. The company operates in areas such as cardiovascular health, diabetes management, diagnostic testing, nutrition, and neuromodulation for chronic pain and movement disorders. Abbott's products include advanced medical devices and diagnostic tests that help healthcare professionals and patients manage health conditions effectively. For example, their cardiovascular technologies assist in heart health management, while diabetes care products enable accurate glucose monitoring without painful fingersticks. Unlike many competitors, Abbott emphasizes accessibility and affordability in its offerings, aiming to make life-changing technologies available to a broader audience. The company's goal is to positively impact global health and well-being, supported by a commitment to sustainability and a 2030 Sustainability Plan.

Lake Bluff, IllinoisHeadquarters

1888Year Founded

IPOCompany Stage

HealthcareIndustries

10,001+Employees