Principal Field Clinical Lead

🔥 4 minutes ago

🏈 Ohio, Michigan, +1 more states – Remote

🏈 Ohio – Remote 🚗 Michigan – Remote 🔔 Pennsylvania – Remote

💵 $99.3k - $198.7k / year

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Abbott

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1888

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare • Healthcare Insurance • Biotechnology

Abbott is a global healthcare company committed to advancing medical technologies and improving lives around the world. It offers a broad range of leading products in diagnostics, medical devices, nutrition, and branded generic medicines. Abbott's innovations such as the FreeStyle Libre glucose monitoring systems and BinaxNOW rapid antigen tests are transforming diabetes management and COVID-19 response. Through its partnerships and initiatives, Abbott aims to foster health equity, improve access to healthcare, and address critical health challenges like malnutrition and infectious diseases. Abbott is also dedicated to sustainability and social responsibility, striving to make life-changing technologies accessible and affordable.

📋 Description

• Manage and develop strategic relationships with clinical trial sites, investigators, and research teams • Support clinical trial execution from site identification and qualification through activation, enrollment, monitoring, and closeout • Maximize patient screening opportunities and achieve enrollment objectives • Identify enrollment barriers and implement recruitment and study-performance solutions • Maintain knowledge of site capabilities, research infrastructure, and investigator interests • Facilitate communication between clinical sites and Abbott teams • Serve as a subject matter expert for TAVI clinical programs and investigational technologies • Provide procedural guidance and technical support during investigational TAVI procedures • Support physicians and healthcare teams with procedural planning, device utilization, and protocol adherence • Partner with commercial field teams when procedural expertise is required • Ensure proper application of study protocols and patient eligibility criteria • Design and deliver education 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 content for investigator meetings, conferences, physician training programs, and internal initiatives • Communicate clinical data, trial objectives, and evidence-based recommendations • Collaborate with Clinical Affairs and Medical Affairs teams on current and future research • Support study design, enrollment strategies, trial performance, and diverse patient enrollment • Partner with Engineering, Clinical Affairs, and Product Development on next-generation TAVI platforms • Provide clinical insights for product enhancements and innovation • Participate in pre-clinical and clinical evaluations, including First-in-Human, Early Feasibility, and IDE trials • Mentor and develop Field Clinical Specialists • Lead cross-functional projects and assist with onboarding, coaching, and personnel development • Identify operational improvements and process standardization opportunities • Conduct activities in accordance with FDA regulations, GCP guidelines, company policies, quality requirements, and study protocols • Ensure accurate and timely documentation and communication of clinical activities • Build collaborative relationships with customers, physicians, investigators, and internal partners • Work cross-functionally with Clinical Affairs, Medical Affairs, Medical Directors, Program Management, Global Clinical Organization, R&D, Engineering, Marketing, and Commercial Structural Heart teams

🎯 Requirements

• Associate degree with 13+ years of relevant experience, or bachelor’s degree with 10+ years of relevant experience, or master’s/advanced degree with 5+ years of relevant experience • Relevant discipline in Biological Sciences, Health Sciences, Nursing, Biomedical Engineering, Clinical Research, or related healthcare/scientific field • 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 training physicians and healthcare staff on advanced cardiovascular procedures • Minimum 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, and structural heart disease therapies • Experience managing physician relationships and supporting high-volume clinical centers • 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 and collaborate 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 • Ability and willingness to travel approximately 50% to 75%, including overnight travel; US and OUS • Flexibility to support physician and customer needs outside standard business hours, including occasional evenings and weekends • Maintain required certifications and training for assigned product lines and study processes

🏖️ Benefits

• Career development with an international company • Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan in the next calendar year • Excellent retirement savings plan with a high employer contribution • Tuition reimbursement • Freedom 2 Save student debt program • FreeU education benefit toward a bachelor’s degree • Training and career development, including onboarding programs and tuition assistance • Competitive compensation, incentives and retirement plans • Medical, dental, vision, wellness and occupational health programs • Paid time off • 401(k) retirement savings with a generous company match • Fast-paced work environment with safety prioritized • Clean, well-lit and temperature-controlled production areas • Company stability and community involvement