Cardiac Data Processing Specialist _ Chennai _ Office Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a v…
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Full-time
associate degree
Competitive Base Salary, Performance Related Incentives, Medical Coverage, Dental Coverage, Vision Coverage, Retirement And Pension Plans
Posted 65d ago
~40 hrs/week
Responsibilities
Review and process cardiac data recordings according to study protocols while ensuring data accuracy and completeness. Collaborate with cross-functional teams and trial sponsors to resolve data discrepancies and maintain regulatory compliance.
Requirements
Requires an associate degree or higher in Life Sciences, Health Sciences, or a related field. Prefers 1-2 years of experience in data coordination, quality assurance, or clinical trials.
Full job description
Cardiac Data Processing Specialist Chennai Office Based
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Cardiac Data Processing Specialist at ICON, you will be responsible for reviewing, processing, and ensure the quality of cardiac data for clinical trials, supporting the delivery of high-quality data and compliance with regulatory standards.
What You Will Do:
Your role will involve delivering cardiac sciences work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
Review and process cardiac data recordings according to study-specific protocols and data acquisition guides.
Perform data quality assurance and correction, ensuring accuracy and completeness of clinical trial data.
Communicate data discrepancies to trial sponsors and sites, and resolve queries using the Query Management System.
Collaborate with Medical Operations and cross-functional teams to support data readiness and project timelines.
Maintain strict confidentiality and compliance with Good Clinical Practice (GCP) and regulatory requirements.
Complete administrative tasks such as time reporting and expense documentation in a timely manner.
Your Profile:
You will bring relevant cardiac sciences experience, along with the following qualifications and skills.
Required qualifications and experience:
Associate degree or higher in a relevant field (Life Sciences, Health Sciences, or related).
1-2 years of experience in data coordination, quality assurance, or clinical trials preferred.
Strong attention to detail and organizational skills.
Excellent communication and problem-solving abilities.
Proficiency in Microsoft Office Suite and familiarity with clinical data systems.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Offices: ICON plc, South County Business Park, Leopardstown, Dublin, D18 X5R3, IE · 123 Smith Street, Farmingdale, New York NY 11735, US · Block 2, Hamilton House, National Technology Park, Limerick, V94 TRW8, IE · 100 Longwater Avenue, Green Park, 3rd Floor, North and South Wings, Reading, England RG2 6GP, GB · 1 Almondview Office Park, West Lothian, Livingston, EH54 6SF, GB
Medical DeviceTherapeuticsGovernment and Public Health SolutionsClinical Research ServicesCommercialisation and OutcomesOncologyValue Based HealthcareClinical TrialsPatient RecruitmentInnovation