BENGALURU · FULLTIME
Configuration & QC Specialist I
ICON plc
Bengaluru · onsite · Posted 7d ago
Sourced from
Not disclosed1–3 yrsfulltimeBengaluru
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Section · 01
About this role
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
You will bring relevant configuration and database systems experience, along with the following qualifications and skills.
Required Qualifications And Experience
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee Please click here to apply
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.
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.
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee Please click here to apply
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Section · 02
Skills
medidata raveclinical data managementClinicalinformData Entry
Section · Company
About ICON Plc
ICON plc
Clinical Research
4.5k+
employees
1990
36 years old
Chennai, Tamil Nadu
India
About
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.
Industries
Clinical ResearchBiotech & Life sciencesPharma
Employee ratings
1,077 reviews
4.0/ 5
Culture
4.1
Career growth
3.2
Work-life
4.2
Employees rate it well for
Work Life Balance219Work Culture153Salary111Senior Management91Career Growth80
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