Icon Plc Hiring Clinical Data Programmer

Welcome to ICON, a global leader in Clinical Research dedicated to advancing and improving patients’ lives. Our success is deeply rooted in the talent and diversity of our teams, which enable us to be a better partner to our customers. Our mission is to set new standards in the healthcare industry, making a positive impact on patients worldwide.

We cultivate a unique ‘Own It’ culture, driven by four core values: Accountability & Delivery, Collaboration, Partnership, and Integrity. As a Clinical Research Organization, we aspire to deliver excellence to our clients and patients at every interaction, ultimately becoming the preferred partner in drug development.

If you share our vision and are passionate about making a difference, we invite you to join our dynamic and supportive team, working alongside some of the industry’s brightest and most friendly professionals.

Vacancies List:

• Company Name: ICON
• Company Address: Chennai, Trivandrum, Bangalore
• Company Website: ICON

Position Title:

Clinical Data Programmer

Job Location:

India – Chennai, Trivandrum, and Bangalore

Job Description:

As a Clinical Data Programmer at ICON, you will play a critical role in our mission. Your responsibilities will include:

• Embracing and embodying ICON’s core values that prioritize People, Clients, and Performance.
• Being an active member of the staff who contributes to the culture of process improvement, focusing on streamlining processes, adding value to our business, and meeting client needs.
• Occasional travel, approximately 0%, both domestically and/or internationally.

In the realm of Clinical Data Management Systems (CDMS), your responsibilities will include:

• Participating in study-specific database setup within at least one CDMS system, such as Oracle RDC, Oracle Inform, Medidata Rave, DataTrak UX EDC, Oracle Clinical, and CRF WorkManager.
• Reviewing database specification documents, including CRF Specifications and Data Validation Specifications (DVS).
• Building clinical study database CRF/database screens as per specifications provided by Clinical Data Programming Leads.
• Creating/programming edit checks, special actions, and derivations as per DVS.
• Collaborating with the centralized CDMS Validation Group to ensure the resolution of programming issues within stipulated timelines.
• Completing and maintaining all study documentation in adherence to ICON procedures.
• Updating study databases as specified by Change Request documents and procedures.
• Troubleshooting and resolving issues related to study building and edit check programming.
• Potential participation in study team meetings.
• Attending sponsor audits and providing assistance as required.
• Contributing to internal user group meetings to share knowledge and stay up-to-date with the latest updates and features.
• Ensuring timely responses to queries and proper routing of unresolved queries to subject matter experts (SMEs).

In Clinical Data Standards (CDS), your role will involve:

• Annotating CRFs in accordance with CDISC published or sponsor-specific guidelines.
• Creating data set specifications as per specified study requirements.
• Programming data sets based on specifications.
• Validating data sets through formal, documented quality control processes.
• Developing data programming specifications according to study requirements.
• Programming clinical data programs per specification.
• Validating clinical data programs through formal, documented QC processes.

Benefits of Working in ICON:

We recognize that our success depends on the quality and dedication of our team. Hence, we’ve established a culture that rewards high performance and nurtures talent. Our benefits include:

• Competitive salary packages benchmarked against industry standards.
• Annual bonuses linked to performance goals.
• A range of health-related benefits for you and your family.
• Competitive retirement plans and related benefits like life assurance.