Principal Field Clinical Specialist

Principal Clinical Field Specialist 

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Youâll 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 high employer contribution

• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelorâs degree.

• A company recognized as a great place to work in dozens of countries around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity 

We have an exciting opportunity for the right candidate to join our rapidly growing clinical team within the Abbott Structural Heart division. We are seeking an experienced Field Clinical Specialist (FCS). Primarily responsibilities will include outstanding management of Pre and Post market Transcatheter Aortic Valve Implant (TAVI) clinical trial execution in an assigned territory. In this role, the FCS supports internal and external customers and cross-functional teams.

Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of STRUCTURAL HEART disease.  We aim to lead the markets we serve by requiring the solutions we offer customers provide an improved benefit/risk profile as compared to existing standards of care; a performance threshold that by definition, guides and ensures the productive output of our engineering, business development, and clinical research efforts result in outcomes that advance the standard of care.

What You'll Work On:

• Effectively manage territory by developing long-standing research partnerships with clinical sites, establishing regular touch points with site investigators and research teams to elevate trial visibility. Supporting site research teams by streamlining screening activities, developing tools and best practices to qualify trial candidates, and identifying barriers to enrollment.

• Acquire critical knowledge of sitesâ clinical research capabilities to support Abbottâs clinical evidence generation strategies.

• Responsible for ensuring timely clinical trial site nominations, qualification assessments, and activations for the Structural Heart Division.

• Be a TAVI Subject Matter Expert (SME) and trainer of FCPS, providing expertise in subject eligibility, training, and case support delivering strong enrollment, outstanding clinical outcomes, and data quality.

• Train physicians, support staff, and research personnel on investigational devices, clinical trial Procedural techniques and protocols.

• Maintain Clinical Investigation Protocol (CIP) expertise, to facilitate appropriate trial subject selection for TAVI clinical trials.

• Provide procedural guidance to physicians when implanting investigational TAVI devices or acting as back-up to commercial clinical support as needed.

• Act as a mentor and trainer to less experienced FCSs within their region or in other parts of the country.

• Coordinate communication with internal and external customers to facilitate efficient and compliant clinical trial execution.

• Develop presentation materials to support Investigator Meetings, National Conferences, as well as TAVI product technical training and best practices.

• Convey franchise clinical evidence and strategy with confidence to physicians and research partners.

• Function as a âpipelineâ between Abbott and the Medical Community, constantly communicating valuable information to internal and external customers (product planning, engineering, marketing, and education).

• Support engineering efforts on next generation TAVI platform development by contributing clinical knowledge to early product design iterations and performing in-vitro / in-vivo device and system evaluations.

• Develop clinical best practices on next generation TAVI platforms and provide procedural case support for all phases of product development, from First in Man through Early Feasibility, and IDE Studies.

• Engage with clinical sites to raise subject diversity awareness in neighboring communities and identify barriers to enrolling a diverse trial population.

• Identify opportunities to establish best practices within the organization.

• Complete and maintain certifications that are relevant to their specific product area.

• Complies with U.S (United States). Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

• Performs other related duties and responsibilities, on occasion, as assigned. These duties may include taking calls on evenings and/or weekends for time-sensitive patient case reviews and customer needs.

• Role will evolve as we scale for professional growth opportunities.

• Assist in managing all other FCPS.

This FCS position works closely with Global Clinical Affairs (GCA) including the Medical Director and Program Management, Global Clinical Organization (GCO) field personnel, and Abbottâs Commercial TAVI team. This position has significant interaction with Study Investigators, Research Coordinators, Physician Assistants, and Nurses. This position is required to execute their job responsibilities within established corporate policies and standard operating procedures.

Required Qualifications:

• Masterâs Degree in Biological Sciences, Engineering, a related field, or equivalent. An advanced credential is preferred.

• An advanced credential in a relevant discipline/concentration such as Biological Sciences. Professional Health Science certification or designation.

• Typically, at least four years of clinical research experience (preferably field clinical affairs) is preferred.

• Significant experience in a field-based role in the medical device industry, particularly experience with Cath Lab/Hybrid OR procedures and protocol.

• Ability to work in a geographically diverse business environment.

• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

• Ability to leverage and/or engage others to accomplish projects.

• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

• Multitasks, prioritizes, and meets deadlines in a timely manner.

• Independent worker with strong organizational and follow-up skills, as well as attention to detail.

• Ability to travel approximately 50% - 75%.

* 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.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on X @AbbottNews.

The base pay for this position is $95,000.00 â $190,000.00. In specific locations, the pay range may vary from the range posted.