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New · posted Nov 3

Abbott · Medical Devices

Clinical Site Lead

  • Remote, US) - Houston, TX territory
  • Remote
  • Full-time
  • Senior & Principal
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EmploymentFull-time
LocationRemote, US) - Houston, TX territory
DeadlineOpen until filled

The role

We are recruiting for a Clinical Site Lead to join our field team for the Houston and surrounding territory, including parts of Texas & Oklahoma. The Clinical Site Lead drives study execution and operational excellence across Abbott Cardiovascular therapies (Vascular, Cardiac Rhythm Management, EP, Structural Heart, and Heart Failure). This new team member is a recognized resource in protocol execution, increasing product and disease state knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research application.  
Additionally, adheres to specified site nomination, qualification, and startup processes. In this role you will lead ongoing training/retraining of all site stakeholders to ensure protocol adherence as well as continuously review, manage, and influence all aspects of site’s recruitment and data collection performance (enrollment, discrepancy resolution, compliance, etc.). The individual proactively utilizes appropriate operational metrics to minimize screen failure, attrition rate, etc. and monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.  
They may also be consulted in the following areas: study design, site payments, site audits, local document review, study documents preparation, and submission to site or competent authority/ethics committee.

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.

What you need

Required Qualifications

•    Bachelor's degree in engineering, science, health science, nursing, or a related field, OR equivalent or related experience in cardiology or clinical research.
•      2 + years of progressively more responsible relevant clinical trial experience in the cardiovascular field.

Ability to travel approximately 50%.

Preferred Qualifications   
•    Competency in catheterization lab and operating room protocol and procedures.

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

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

What you'll do

What You’ll Work On

With limited direction from leadership:  
1. Develop and maintain a productive clinical territory:  
Identify, develop, and maintain sites capable of delivering start-up goals, study participation levels and required data quality.  
Understand and assess investigators’ interests and qualifications.  
Identify appropriate investigators as defined by study-specific requirements and by the applicable regulatory code.  
Maintain open communication and relationships with key site personnel including the Principle Investigator, Research Coordinator, as well as regulatory and legal personnel.  
Provide ongoing technical support to customers and field staff.  
Facilitate communication between clinical sites and other Abbott clinical staff (e.g., operations management, study team, Site Contracts Associate), as needed.  
2. Manage all aspects of study lifecycle to include site regulatory and quality:  
Start Up, nominate, approach, and complete qualification processes including establishing site/sponsor expectations for study execution.  
Facilitate all aspects of the start-up process and site initiation visits  
Understand regulatory and legal requirements for study participation at a level that allows for appropriate collaboration with Abbott clinical staff, e.g. Site CRA, Site Contract Associate.  
Train facility staff regarding protocol requirements and technology.  
Enrollment  
Develop site-specific strategies to promote appropriate patient enrollment.  
Identify site successes and challenges and assist in implementing techniques that promote study goal achievement.  
Continuously evaluate site study performance and provide timely feedback to site.  
Attend study procedures and follow-ups when indicated (or ensure trained personnel attend).  
Regulatory and Quality  
Core level Abbott certification and/or equivalent level proficiency  
Develop site-specific strategies to avoid deviations.  
Educate site on tools to facilitate compliance.  
Provide timely feedback to the sites on key compliance indicators.  
Escalate non-compliant sites according to corporate policy.  
Collect essential documents, identify and obtain missing data, data corrections, reviewing adverse events and protocol deviations.  
Review data and source documentation from investigational sites for accuracy and completeness  
Facilitate resolution of data queries and action items at clinical sites  
Promptly reports the findings of monitoring visits according to Abbott processes.  
Maintain accurate, detailed and complete records of monitoring visits.  
3. Provide training and procedure coverage:  
Apply clinical and technical expertise to train site and Abbott staff for clinical trials and applicable commercial launches.  
As needed, provide clinical and technical expertise for clinical trial procedure support  
Attend study procedures and follow-ups (or ensure trained personnel attend).  
4. Collaborate with commercial partners:  
When appropriate, collaborate in the education of local sales groups on new product launches.  
When appropriate, contribute to the education of customers on new and existing Abbott products.  
Meet with key customers where Abbott GCO presence can elevate the customer experience.  
Act as an additional resource for technical questions and troubleshooting.  
5. Identify and adapt to shifting priorities and competing demands.  
6. Remain current on developments in the field of expertise including clinical and Abbott product knowledge, competitive positioning and published scientific and economic evidence.  
Maintain at least one area of expertise and function as a local clinical and technical resource.  
7. Possess independent problem-solving skills and ability to make decisions.  
8. Exhibit excellent oral and written communication skills. 

Pay and benefits

$61,300 – $122,700 a year

Employer provided
How this compares

The base pay for this position is

$61,300.00 – $122,700.00

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

  • Free medical coverage (Health Investment Plan PPO)

  • Retirement savings plan with high employer contribution

  • Tuition reimbursement

  • Freedom 2 Save student debt program

  • FreeU education benefit

  • Career development

Working conditions

Standard

TRAVEL

Yes, 50 % of the Time

MEDICAL SURVEILLANCE

No

JOB FAMILY

Clinical Affairs / Statistics

DIVISION

MD Medical Devices

LOCATION

United States of America : Remote

Smiling Abbott colleagues in Abbott T-shirts packing disaster relief boxes together

From the posting

About Abbott

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. 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 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 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.

Abbott company page · 107 open roles
Equal opportunity, accessibility and legal noticesAbbott's statements, word for word

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.

Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

Job intelligence

The context around this role

Live data · November 3, 2026

Salary intelligence

How the pay compares

This role's midpoint is 26% below the US median for Clinical Research roles at this level.

This roleEmployer provided

$61,300 to $122,700 a year

Senior & Principal roles in the US51 roles publishing pay

Middle half $120,250 to $130,500, median $124,500
Annual base pay
Annual base payLowMedianHigh
This role$61,300—$122,700
All US$120,250$124,500$130,500

This role: Abbott's own published range. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Research

The general path across 210 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not Abbott's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Clinical Research Associate · Clinical Research Coordinator

    $103K median113 open
  2. This role

    Senior & Principal

    Often: Senior Clinical Research Associate · Sr. CRA

    $125K median92 open
  3. Next step

    Manager

    Often: Associate Clinical Research Manager · Senior Clinical Research Manager

  4. Later

    Director

    Often: Associate Director, Site Monitoring · Director, Clinical Trial Liaison

Skills DNA

What this role leans on

How many of the posting's 8 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesDocumentation and SOPs: 3 linesInvestigations and CAPA: 1 lineValidation and qualification: 2 linesRegulatory submissions: 1 lineClinical trial conduct: 4 linesCollaboration and leadership: 3 linesGMPDocumentationInvestigationsValidationSubmissionsClinical trialsTeamwork
  • Clinical trial conduct4
  • Documentation and SOPs3
  • Collaboration and leadership3
  • GMP and compliance2
  • Validation and qualification2
  • Investigations and CAPA1
  • Regulatory submissions1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

Abbott on Regulatory Jobs

107
Open roles
97
Distinct roles
33
Locations

By discipline

  • Quality59 55%
  • Regulatory30 28%
  • Clinical17 16%

By level

  • Senior & Principal50 47%
  • Associate & Specialist32 30%
  • Manager21 20%
See all 107 Abbott roles

More roles at Abbott

All 107 Abbott roles

Similar Clinical Research roles elsewhere

Clinical Site Lead at Abbott

Open until filled. $61K–$123K a year, employer provided.

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