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New · posted Nov 1

Abbott · Medical Devices

Sr. Clinical Site Lead

  • Remote, US
  • Remote
  • Full-time
  • Senior & Principal
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EmploymentFull-time
LocationRemote, US
DeadlineOpen until filled

The role

The Clinical Site Lead drives study execution and operational excellence across Abbott Cardiovascular therapies (Vascular, Cardiac Rhythm Management, EP, Structural Heart, and Heart Failure). 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.

Adheres to specified site nomination, qualification, and startup processes. Leads ongoing training/retraining of all site stakeholders to ensure protocol adherence. Continuously reviews, manages, and influences all aspects of site’s recruitment and data collection performance (enrollment, discrepancy resolution, compliance, etc.). Proactively utilizes appropriate operational metrics to minimize screen failure, attrition rate, etc. Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.

May 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.  

  • Competency in catheterizaion lab and operating room protocol and procedures.

  • Ability to travel approximately 75%, including internationally.

What you'll do

What You’ll Work On

With limited direction from leadership:

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.

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.

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).

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.

  • Identify and adapt to shifting priorities and competing demands. 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.

  • Develop working knowledge of disease states and product lines for all relevant Abbott clinical trials.

  • Upon leadership approval, complete and maintain certifications that are relevant to specific field(s) of expertise (where appropriate).

  • Possess independent problem-solving skills and ability to make decisions.
  • Exhibit excellent oral and written communication skills.

Pay and benefits

$78,000 – $156,000 a year

Employer provided
How this compares

The base pay for this position is

$78,000.00 – $156,000.00

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

  • Free medical coverage through Health Investment Plan (HIP) PPO

  • Retirement savings plan with high employer contribution

  • Tuition reimbursement

  • Freedom 2 Save student debt program

  • FreeU education benefit

Working conditions

Standard

TRAVEL

Yes, 75 % of the Time

MEDICAL SURVEILLANCE

Not Applicable

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

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

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 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.
Abbott company page · 108 open roles
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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.

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Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 6% below the US median for Clinical Research roles at this level.

This roleEmployer provided

$78,000 to $156,000 a year

Senior & Principal roles in the US50 roles publishing pay

Middle half $123,750 to $130,500, median $124,500
Annual base pay
Annual base payLowMedianHigh
This role$78,000—$156,000
All US$123,750$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 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Research

The general path across 193 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

    $110K median102 open
  2. This role

    Senior & Principal

    Often: Senior Clinical Research Associate · Sr. CRA

    $125K median87 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 35 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesDocumentation and SOPs: 5 linesInvestigations and CAPA: 4 linesValidation and qualification: 2 linesRegulatory submissions: 1 lineClinical trial conduct: 13 linesCollaboration and leadership: 13 linesGMPDocumentationInvestigationsValidationSubmissionsClinical trialsTeamwork
  • Clinical trial conduct13
  • Collaboration and leadership13
  • Documentation and SOPs5
  • GMP and compliance4
  • Investigations and CAPA4
  • Validation and qualification2
  • 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

108
Open roles
98
Distinct roles
32
Locations

By discipline

  • Quality61 56%
  • Regulatory30 28%
  • Clinical16 15%

By level

  • Senior & Principal50 46%
  • Associate & Specialist33 31%
  • Manager21 19%
See all 108 Abbott roles

More roles at Abbott

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Similar Clinical Research roles elsewhere

Sr. Clinical Site Lead at Abbott

Open until filled. $78K–$156K a year, employer provided.

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