Clinical Site Lead

🔥 14 hours ago

🤠 Texas – Remote

🤠 Texas – Remote

💵 $61.3k - $122.7k / 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

• Drive study execution and operational excellence across Abbott Cardiovascular therapies • Support protocol execution, product and disease-state knowledge, procedure support, procedure outcomes, trend identification, clinical trial enrollment, and ICH-GCP application • Adhere to site nomination, qualification, and startup processes • Lead ongoing training and retraining of site stakeholders to ensure protocol adherence • Manage site recruitment and data collection performance, including enrollment, discrepancy resolution, and compliance • Use operational metrics to minimize screen failure and attrition • Monitor compliance with regulatory requirements, Good Clinical Practice, and accuracy standards through site initiation, periodic, and close-out visits • Develop and maintain a productive Dallas-area clinical territory and qualified clinical sites • Assess investigators and identify appropriate investigators according to study-specific and regulatory requirements • Maintain relationships with principal investigators, research coordinators, regulatory personnel, and legal personnel • Provide technical support to customers and field staff • Facilitate communication between clinical sites and Abbott clinical staff • Manage study startup, enrollment, regulatory, and quality activities • Nominate and qualify sites, establish execution expectations, and facilitate site initiation visits • Train facility staff on protocol requirements and technology • Develop site-specific enrollment and deviation-avoidance strategies • Evaluate site performance and provide feedback • Attend study procedures and follow-ups or ensure trained personnel attend • Collect essential documents, obtain missing data, review adverse events and protocol deviations • Review source documentation and investigational-site data for accuracy and completeness • Resolve data queries and action items • Report monitoring-visit findings and maintain complete monitoring records • Train site and Abbott staff for clinical trials and commercial launches • Collaborate with commercial partners on product education and customer support • Provide technical troubleshooting and clinical expertise • Adapt to shifting priorities and competing demands • Maintain an area of clinical and technical expertise

🎯 Requirements

• Associates Degree • 1 year experience • Preferred: Bachelor’s Degree or Master’s Degree in engineering, science, health science, nursing, or a related field, or equivalent or related experience in cardiology or clinical research • Preferred: 2+ years of progressively more responsible relevant clinical trial experience in the cardiovascular field • Preferred: Competency in catheterization lab and operating room protocol and procedures • Preferred: Ability to travel approximately 50% • Core level Abbott certification and/or equivalent level proficiency • Excellent oral and written communication skills • Independent problem-solving skills and ability to make decisions • Ability to remain current on clinical and Abbott product knowledge, competitive positioning, and published scientific and economic evidence

🏖️ Benefits

• Career development with an international company • Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan • Retirement savings plan with high employer contribution • Tuition reimbursement • Freedom 2 Save student debt program • FreeU education benefit • Employee diversity and workplace recognition programs