ICON
Configuration & QC Specialist I
India · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerICON
- LocationIndia
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Configuration & QC Specialist I
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 Configuration & QC Specialist I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to configuration and database systems activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Assisting in the configuration and setup of clinical trial databases and electronic data capture (EDC) systems, ensuring accuracy and adherence to project specifications.
- Performing quality control (QC) checks on clinical trial data and study documentation to identify discrepancies, inconsistencies, and data entry errors.
- Collaborating with cross-functional teams including data management, biostatistics, and clinical operations to address QC findings and ensure data integrity and reliability.
- Supporting the development and implementation of validation plans and procedures to assess the functionality and performance of EDC systems and data management processes.
- Providing training and support to end-users on system configuration, data entry guidelines, and QC processes to promote compliance and efficiency.
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Your Profile:
You will bring relevant configuration and database systems experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- 1+ years of experience in clinical data management, data entry, or related role, preferably within the pharmaceutical or biotechnology industry.
- Familiarity with clinical trial databases and electronic data capture (EDC) systems, such as Medidata Rave, Oracle Clinical, or Inform.
- Strong attention to detail and analytical skills, with the ability to identify and resolve data-related issues.
- Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
- Proactive attitude with a willingness to learn and adapt to evolving technologies and processes.
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
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked