Clinical Monitoring Lead
Quick Summary
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,
What We Offer
~1 min readThe Clinical Monitoring Lead (CML) supports clinical monitoring quality, oversight, and execution within an assigned region. This role partners with Clinical Site Management Leadership to support monitoring excellence through monitoring activities, compliance support, monitoring documentation review, issue resolution, and continuous improvement efforts.
The CML collaborates with Clinical Site Leads, study teams, and quality partners to support consistent execution of monitoring plans, regulatory compliance, timely issue resolution, and adherence to company standards. The CML serves as a key monitoring resource, helping ensure high-quality monitoring practices and inspection readiness across assigned studies.
The CML demonstrates proficiency in Site Quality Monitoring, KCI process, SIV, PMV, and COV activities and develops expertise in monitoring-related clinical data systems and study-specific Monitoring Plans. In addition to monitoring assigned sites, the CML supports monitoring training, execution, and best practice implementation throughout the region while collaborating with Field Clinical Quality Managers and cross-functional study teams.
May be consulted in the following areas: study and CRF design, site audits, local document review and study document preparation. The CML contributes to successful study execution by supporting high-quality monitoring practices, compliance, and operational effectiveness.
$61,300.00 – $122,700.00In specific locations, the pay range may vary from the range posted.
- Monitor clinical studies at sites within an assigned territory (and others as requested) to ensure compliance with study requirements, Good Clinical Practice (GCP), applicable regulations, and company procedures.
- Review monitoring documentation and monitoring activities for quality, completeness, and compliance with study requirements.
- Support monitoring issue identification, escalation, and resolution activities.
- Contribute to inspection readiness activities and support monitoring-related quality initiatives.
- Assist with review of monitoring trends and quality metrics to support consistency and continuous improvement.
- Support onboarding and training of Clinical Site Leads and monitoring personnel on monitoring processes.
- Participate in monitoring-focused training initiatives and sharing of best practices.
- Collaborate with study teams, Clinical Site Leads, and quality partners to address monitoring-related questions and issues.
- Partner with study teams and regional leadership to support monitoring performance, quality objectives, and study execution goals.
- Support implementation and maintenance of monitoring tools, processes, and operational resources.
- Identify opportunities to improve monitoring quality, efficiency, and consistency.
- Escalate significant compliance or quality concerns according to company policies and procedures.
- Participate in projects and initiatives that improve monitoring effectiveness, quality, compliance, and operational efficiency.
- Support audit, inspection, and quality-related activities as requested.
- Remain current on clinical research regulations, GCP requirements, monitoring practices, and applicable therapeutic-area knowledge.
Requirements
~1 min read- Bachelor's degree or an equivalent combination of education and work experience.
- 3 years' experience in a clinical research environment or other equivalent experience.
- Knowledge of regulations and standards (Good Clinical Practices) for conducting clinical research.
- Polished communicator: written documentation and oral presentations/discussions/meetings.
- Ability to work in a highly matrixed and geographically diverse business environment.
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Ability to leverage and/or engage others to accomplish projects.
- Strong verbal and written communication skills with ability to effectively communicate at multiple levels in the organization.
- Ability to multitask, prioritize, and meet deadlines in a timely manner.
- Strong organizational and follow-up skills, as well as attention to detail.
- Experience and training on GCP.
- Bachelor's degree in Engineering, Biological Sciences, Nursing, or a related field OR equivalent or related experience in cardiology or clinical research.
- 2 years' experience as a field clinical monitor.
- 3 to 5 years of relevant clinical trial experience in the cardiovascular and/or Neuromodulation field.
- 2+ years of medical device experience.
- Experience with GCP, ISO standards, and clinical trial guidelines.
- Flexibility to work across all U.S. time zones.
- Experience supporting monitoring activities, monitoring quality, compliance initiatives, audit readiness, or inspection support activities.
- Demonstrated ability to evaluate monitoring activities and identify opportunities for process improvement.
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.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Location & Eligibility
Listing Details
- First seen
- September 27, 2026
- Last seen
- September 27, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 65%
- Scored at
- September 27, 2026
Signal breakdown
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