Job Description
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
Responsibilities:
• Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
• Create data set specifications per specified study requirements.
• Program data sets per specification.
• Validate data sets per the formal, documented QC process.
• Create data programming specifications per specified study requirements.
• Program clinical data programs per specification.
• Validate clinical data programs per the formal, documented QC process.
• Review and quality assure CRF, data set and programming specifications, program code and outputs.
• Create and maintain study documentation as required, in accordance with ICON Standard Operating Procedures.
• Execute programs and generate clinical data outputs to according to study/client requirements.
• Participate in testing of clinical data system upgrades and documenting of test scripts when required.
• Adhere to Data Management department quality control procedures.
• Liaise with other ICON functions & sponsors as needed.
• To undertake other reasonably related duties as may be assigned from time to time.
• Contribute to department process improvements, SOPs and WPs
• Demonstrable expertise with CDISC CDASH, SDTM, CRT-DDS, ADaM, and controlled terminology.
• Manage multiple projects, ensuring that timelines are met and deliverables are of sufficient quality
• Presentation and attendance at appropriate scientific meetings and conferences.
Required Skills:
• Demonstrated ability to produce programmed clinical data deliverables (CDS only).
• Ability to successfully manage multiple tasks and timelines.
• Ability to perform assigned tasks with little supervision.
• Ability to liaise professionally with team members.
• Team player with strong verbal and written communication skills.
• Demonstrated ability to learn new technologies, applications and techniques.
• Expert knowledge of the clinical data programming development life cycle.
• Expert knowledge of clinical data programming concepts.
• Knowledge of SQL programming desirable.
• Advanced knowledge of SAS programming.
PROCESS
Technical and competency selection:
When you spot an opportunity you're interested in and submit an application, one of our Talent Acquisition Specialists will contact you to evaluate your suitability for this position, as well as for other openings within the business. The evaluation will look at your technical skills and your competencies – for example, delivering excellence.
Interview
After this, we'll let you know if we'll be progressing with your application. If you have been successful at this stage, we will talk you through a telephone interview. This will then be followed by an interview with our Hiring Manager, either face to face or by tele-conference.
Offer
If you're successful, we will notify you with details of the offer, talk you through our culture and values, answer any questions you may have – and above all, welcome you to the ICON team
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
Responsibilities:
• Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
• Create data set specifications per specified study requirements.
• Program data sets per specification.
• Validate data sets per the formal, documented QC process.
• Create data programming specifications per specified study requirements.
• Program clinical data programs per specification.
• Validate clinical data programs per the formal, documented QC process.
• Review and quality assure CRF, data set and programming specifications, program code and outputs.
• Create and maintain study documentation as required, in accordance with ICON Standard Operating Procedures.
• Execute programs and generate clinical data outputs to according to study/client requirements.
• Participate in testing of clinical data system upgrades and documenting of test scripts when required.
• Adhere to Data Management department quality control procedures.
• Liaise with other ICON functions & sponsors as needed.
• To undertake other reasonably related duties as may be assigned from time to time.
• Contribute to department process improvements, SOPs and WPs
• Demonstrable expertise with CDISC CDASH, SDTM, CRT-DDS, ADaM, and controlled terminology.
• Manage multiple projects, ensuring that timelines are met and deliverables are of sufficient quality
• Presentation and attendance at appropriate scientific meetings and conferences.
Required Skills:
• Demonstrated ability to produce programmed clinical data deliverables (CDS only).
• Ability to successfully manage multiple tasks and timelines.
• Ability to perform assigned tasks with little supervision.
• Ability to liaise professionally with team members.
• Team player with strong verbal and written communication skills.
• Demonstrated ability to learn new technologies, applications and techniques.
• Expert knowledge of the clinical data programming development life cycle.
• Expert knowledge of clinical data programming concepts.
• Knowledge of SQL programming desirable.
• Advanced knowledge of SAS programming.
PROCESS
Technical and competency selection:
When you spot an opportunity you're interested in and submit an application, one of our Talent Acquisition Specialists will contact you to evaluate your suitability for this position, as well as for other openings within the business. The evaluation will look at your technical skills and your competencies – for example, delivering excellence.
Interview
After this, we'll let you know if we'll be progressing with your application. If you have been successful at this stage, we will talk you through a telephone interview. This will then be followed by an interview with our Hiring Manager, either face to face or by tele-conference.
Offer
If you're successful, we will notify you with details of the offer, talk you through our culture and values, answer any questions you may have – and above all, welcome you to the ICON team
💡 Quick Summary
Seeking a career-building opportunity? The Senior Clinical Data Programmer position is now open for candidates interested in the Software Developer Jobs sector. This role in Chennai offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Software Developer Jobs is a plus.
