Senior Clinical Scientist

Senior Clinical Scientist Apply locations United States - Minnesota - St. Paul

Time type Full time

Posted on Posted 6 Days Ago

Time left to apply End Date: December 6, 2024 (9 days left to apply)

Job requisition id 31103714

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION: Senior Clinical Scientist Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

Career development with an international company where you can grow the career you dream of. Free medical coverage for employees* via the Health Investment Plan (HIP) PPO. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our St. Paul, MN location, supporting transfemoral transcatheter mitral valve replacement (TF TMVR). The Senior Clinical Scientist will support scientific activities associated with the design, conduct, and reporting of clinical trials for this therapeutic area. At Abbott, we're advancing the treatment of heart disease through breakthrough, minimally-invasive medical technologies, restoring health and allowing people to get on with their lives.

What You'll Work On: This position will work closely with the clinical study team including project management, biostatistics, data management, and other clinical study personnel. This position will have significant interaction with the clinical site personnel to ensure excellent patient outcomes. Furthermore, this position will be required to execute job responsibilities within the corporate policies and standard operating procedures. Additionally this position:

Supports senior clinical personnel in the development 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 and writes study-related documents and/or contributes content of such documents, including, but not limited to, clinical study reports, clinical study protocols, case report forms, investigational brochures, and informed consent forms. Will assist in the development of procedures and methods aimed at ensuring excellent patient clinical outcomes during the conduct of clinical studies. Supports senior clinical personnel 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, and external stakeholders including steering committees, study leadership, and publication committees. Supports the development of the scientific podium and publication strategy in close collaboration with cross-functional teams and leads the execution of the publication strategy through coordination with investigator authors and internal teams. Serves as an active member of study teams and provides scientific support to justify trial design and ongoing scientific analysis during protocol development. May include generation of pre-protocol documentation of scientific information. Supports the review and analysis of statistical analysis plans. Generates documents to support regulatory submissions for Abbott products and/or responds to questions from regulatory authorities about existing submissions. Required Qualifications: Advanced degree in the sciences, medicine, or similar discipline. 5+ years of related work experience with a solid understanding of specified functional area, or an equivalent combination of education and work experience. Demonstrated scientific writing ability. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Independent decision making required. 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. Experience working on regulated, pre-market clinical studies. Experience working in a quality system environment. Preferred Qualifications: Experience conducting mitral valve replacement (TS TMVR in particular) trials preferred. Early Feasibility Study (EFS) experience preferred. Pre-market approval (PMA) application experience preferred. Experience evaluating and contracting CROs, scientific core labs, and establishing and managing trial Steering Committees preferred. Experience overseeing and conducting Medical Advisory Board (MAB) meetings preferred. Master's degree in the sciences, medicine, or similar discipline preferred. * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

The base pay for this position is $83,000.00 – $166,000.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Medical & Scientific Affairs

DIVISION:SH Structural Heart

LOCATION:United States > Minnesota > St. Paul > Woodridge : 177 East County Rd B

WORK SHIFT:Standard

TRAVEL:Yes, 5 % of the Time

MEDICAL SURVEILLANCE:No

SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf About Us Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it's next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

The people of Abbott come to work each day with relentless energy, enthusiasm, and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life's greatest health challenges.

We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

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