Abbott Posted September 30, 2026

Principal Field Clinical Lead- Houston or Dallas, TX

Abbott Park, Illinois, United States FULL_TIME
Notify me about similar jobs

Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 122,000 colleagues serve people in more than 160 countries.

Principal Field Clinical Lead

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.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

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

Within Abbott's Structural Heart business, our mission is to restore health and improve quality of life through innovative solutions for the treatment of structural heart disease. We are committed to developing technologies that improve patient outcomes, advance clinical practice, and provide meaningful benefits for physicians, healthcare systems, and the patients they serve.

As a global leader in transcatheter heart valve technologies, Abbott continues to invest in clinical research, physician education, and next-generation therapies that shape the future of structural heart interventions.

Abbott Structural Heart is seeking a highly experienced Principal Field Clinical Lead (FCL) to support pre-market and post-market Transcatheter Aortic Valve Implantation (TAVI) clinical studies within an assigned territory.

In this senior clinical role, the Principal FCL serves as a key partner to physicians, study investigators, research coordinators, and internal stakeholders to ensure successful clinical trial execution, exceptional patient outcomes, and high-quality clinical data.

The Principal FCSL functions as a clinical and procedural expert, providing physician education, procedural support, site management, enrollment strategy, and clinical trial leadership. This individual will also contribute to the development of future TAVI technologies by partnering with Clinical Affairs, Research & Development, Engineering, and Commercial teams to advance Abbott's structural heart portfolio.

Success in this role requires a deep understanding of structural heart disease, transcatheter valve therapies, clinical research operations, and physician training within Cath Lab and Hybrid Operating Room environments.

What You’ll Work On

Clinical Trial Leadership & Site Management

Manage and develop strategic relationships with assigned clinical trial sites, investigators, and research teams.

Support all phases of clinical trial execution, including site identification, qualification, activation, enrollment, monitoring, and study closeout activities.

Collaborate with investigators and site personnel to maximize patient screening opportunities and achieve enrollment objectives.

Identify enrollment barriers and implement solutions that improve patient recruitment and study performance.

Maintain a comprehensive understanding of site capabilities, research infrastructure, and investigator interests to support Abbott's clinical evidence generation strategy.

Facilitate communication between clinical sites and Abbott teams to ensure efficient study execution and issue resolution.

TAVI Clinical and Procedural Support

Serve as a subject matter expert for Abbott's TAVI clinical programs and investigational technologies.

Provide procedural guidance and technical support during investigational TAVI procedures.

Support physicians and healthcare teams in procedural planning, device utilization, and study protocol adherence.

Partner with commercial field teams when additional procedural expertise is required.

Ensure proper application of study protocols and eligibility criteria for patient selection.

Maintain expertise in current and emerging structural heart therapies, competitive technologies, and evolving treatment strategies.

Physician and Clinical Staff Education

Design and deliver educational programs for physicians, research coordinators, physician assistants, nurses, and Cath Lab personnel.

Train healthcare professionals on investigational devices, clinical protocols, procedural best practices, and study requirements.

Develop educational content and presentation materials for: Investigator Meetings

National and regional conferences

Physician training programs

Internal educational initiatives

Serve as a trusted clinical resource for both internal and external stakeholders.

Clinical Evidence and Research Support

Support the generation and dissemination of clinical evidence related to Abbott's TAVI portfolio.

Effectively communicate clinical data, trial objectives, and evidence-based recommendations to healthcare professionals.

Collaborate with Global Clinical Affairs and Medical Affairs teams to support ongoing and future research initiatives.

Assist in identifying opportunities to improve study design, enrollment strategies, and overall trial performance.

Promote diverse and representative patient enrollment across clinical trials.

Product Development and Innovation

Partner with Engineering, Clinical Affairs, and Product Development teams to support next-generation TAVI platform development.

Provide real-world clinical insights that inform product design enhancements and future innovation efforts.

Participate in pre-clinical and clinical evaluations of emerging technologies.

Assist in developing procedural best practices for new platform introductions and early-stage clinical evaluations, including: First-in-Human Studies

Early Feasibility Studies

IDE Clinical Trials

Leadership and Mentorship

Mentor and develop less-experienced Field Clinical Leads.

Share best practices and support the ongoing development of field clinical teams.

Provide leadership across cross-functional projects and initiatives.

Assist management with onboarding, coaching, and development of clinical personnel as needed.

Identify opportunities for operational improvements and process standardization across the organization.

Compliance and Quality

Conduct all activities in accordance with: FDA regulations

Good Clinical Practice (GCP) guidelines

Company policies and procedures

Quality system requirements

Clinical study protocols

Maintain all required certifications and training for assigned product lines and study processes.

Ensure accurate and timely documentation and communication of clinical activities.

Foster professional and collaborative relationships with customers, physicians, investigators, and internal partners

This position works closely with / Cross-functional Partnerships:

Global Clinical Affairs (GCA)

Medical Directors

Program Management Teams

Global Clinical Organization (GCO)

Research & Development

Engineering

Marketing

Medical Affairs

Commercial Structural Heart Teams

The role also requires significant interaction with:

Interventional Cardiologists

Cardiac Surgeons

Study Investigators

Research Coordinators

Cath Lab Staff

Physician Assistants

Nurse Practitioners

Registered Nurses

Required Qualifications

Education

Associate degree with 13+ years of relevant experience, or

Bachelor's degree with 10+ years of relevant experience, or

Master's degree or advanced degree with 5+ years of relevant experience.

Relevant disciplines include:

Biological Sciences

Health Sciences

Nursing

Biomedical Engineering

Clinical Research

Other related healthcare or scientific fields

Experience

Significant experience supporting implants and procedures involving complex transcatheter valve technologies.

Extensive experience within a structural heart or transcatheter valve medical device organization.

Previous experience providing physician and healthcare staff training on advanced cardiovascular procedures.

Minimum of 4 years of clinical research experience, preferably within Field Clinical Affairs or Medical Device Clinical Operations.

Strong understanding of: TAVI/TAVR procedures

Clinical trial execution

Cath Lab workflows

Hybrid Operating Room environments

Structural heart disease therapies

Experience managing physician relationships and supporting high-volume clinical centers.

Knowledge, Skills & Competencies

Deep clinical and procedural knowledge of structural heart therapies.

Exceptional presentation and physician training skills.

Strong leadership and mentoring capabilities.

Ability to influence without direct authority.

Excellent written and verbal communication skills.

Strong organizational and project management abilities.

Ability to work independently while effectively collaborating across cross-functional teams.

Skilled at managing multiple priorities in a fast-paced environment.

High attention to detail and commitment to quality.

Ability to build credibility and trust with physicians, investigators, and internal stakeholders.

Travel Requirements

Ability and willingness to travel approximately 50% to 75%, including overnight travel as required. US and OUS

Flexibility to support physician and customer needs outside standard business hours, including occasional evenings and weekends.

Apply Now

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 $99,300.00 – $198,700.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Principal
Function
Clinical Development
Therapeutic area
Not listed
Location
Abbott Park, Illinois, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 403 comparable Principal Clinical Development roles across 64 biopharma companies.

403Comparable roles tracked
382Currently active
64Companies hiring similar roles
34Countries represented

Salary context

172 of 403 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Patient Safety, Medical Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $392,100 (median $253,000)

Where these roles are based

Top locations among the 403 comparable roles

United States253
India40
United Kingdom21
China10
Taiwan8
Spain7

+ 28 more countries

Seniority mix

403 of 403 peers have a known seniority level

Director219
Senior143
Principal41

Therapeutic area mix

86 of 403 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology50
Neuroscience11
Immunology7
Respiratory6
Cardiovascular / CVRM5
Dermatology & Aesthetics3
Ophthalmology3
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Johnson & Johnson Raritan, United States Principal
Same function Same seniority Same country
60%similar
Merck North Wales, Pennsylvania, United States of America Principal
Same function Same seniority Same country
60%similar
Johnson & Johnson Raynham, United States Principal
Same function Same seniority Same country
60%similar
Merck North Wales, Pennsylvania, United States of America Principal
Same function Same seniority Same country
60%similar
Neurocrine Biosciences Inc. US CA San Diego, United States Principal
Same function Same seniority Same country
60%similar
Neurocrine Biosciences Inc. US CA San Diego, United States Principal
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Principal Scientist, Clinical Pharmacology & Pharmacometrics
Johnson & Johnson · Raritan, United States · Principal
Function Therapeutic area Seniority Country
60%
Sr Principal Clinical Engineer
Johnson & Johnson · Raynham, United States · Principal
Function Therapeutic area Seniority Country
60%
Sr. Principal Scientist, Clinical Pharmacology
Neurocrine Biosciences Inc. · US CA San Diego, United States · Principal
Function Therapeutic area Seniority Country
60%
Principal Scientist, Translational Medicine, Neuroscience
Merck · West Point, Pennsylvania, United States of America · Principal
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.