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À propos de ce poste Cardiac Specialist I chez Clario

Clario · Télétravail · Costa Rica Remote

At Clario, a part of Thermo Fisher Scientific, we help transform lives by unlocking better evidence that accelerates the development of life-changing therapies. As a Cardiac Specialist I, you will play a critical role in the analysis and processing of cardiac safety data used in global clinical trials. Working in a remote production environment, you will perform electrocardiogram (ECG) measurements, Holter and Ambulatory Blood Pressure Monitoring (ABPM) data processing, and safety assessments while ensuring the highest levels of quality, accuracy, and regulatory compliance. This is an excellent opportunity for professionals with a strong cardiovascular foundation who are passionate about clinical research, patient safety, and data integrity.

 

What We Offer

  • Competitive compensation
  • Private medical and dental insurance
  • Life insurance coverage
  • Annual bonus (Aguinaldo) and vacation benefits in accordance with Costa Rican legislation
  • Remote work flexibility
  • Wellness and learning programs that support professional growth and career development

 

What You'll Be Doing

  • Perform interval duration and heart rate measurements on digital and paper ECGs in accordance with established Standard Operating Procedures (SOPs).
  • Analyze ECG waveforms, place digital calipers, and perform measurement adjustments utilizing approved methodologies.
  • Use validated software tools to convert cardiac image files into XML format and verify conversion accuracy.
  • Calibrate and scale PDF-based ECG records to ensure accurate cardiac measurements.
  • Process cardiac safety data from continuous Holter recordings.
  • Extract protocol-specific 12-lead ECG time points and export XML files to designated databases for measurement activities.
  • Evaluate cardiac safety data for alert findings and follow escalation procedures when clinically significant observations are identified.
  • Perform Ambulatory Blood Pressure Monitoring (ABPM) processing activities.
  • Manage multiple workflows and prioritize assignments according to operational requirements and business priorities.
  • Participate in quality assurance programs to demonstrate accuracy, precision, consistency, and repeatability.
  • Maintain compliance with SOPs, work instructions, regulatory requirements, and departmental standards.
  • Meet or exceed established productivity, quality, and turnaround-time metrics.
  • Identify and report system or application performance issues through appropriate management and technical support channels.
  • Contribute to continuous improvement initiatives that enhance quality, efficiency, and customer satisfaction.

 

What We Look For

  • Associate's degree, ECG certification, or an equivalent combination of education and experience required.
  • Bachelor's degree in healthcare, life sciences, or related field preferred.
  • Strong knowledge of cardiovascular physiology and anatomy.
  • 1 to 2 years of experience in an ECG Core Laboratory, cardiac diagnostics environment, clinical research organization, or related healthcare setting.
  • Experience working in environments governed by GCP, GDPR, and data privacy regulations preferred.
  • Experience processing ECG, Holter, cardiac telemetry, or other cardiac safety data.
  • Strong computer skills, including Microsoft Office applications, Google Workspace, Excel, and database systems.
  • Ability to work independently, demonstrate initiative, and solve problems effectively.
  • Strong organizational skills and ability to manage competing priorities within a metrics-driven production environment.
  • Excellent attention to detail and commitment to data quality.
  • Strong verbal and written English communication skills.
  • Ability to collaborate effectively within a team environment while maintaining high individual productivity.
  • Positive, proactive, and customer-focused approach to work.
  • Ability to work remotely from Costa Rica while maintaining productivity and quality expectations.

At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.


Clario, a part of Thermo Fisher Scientific is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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À propos de Clario

Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 20

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