Clinical Data Programmer
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please see similar roles below...
*LI-NM1
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As Clinical Data Programmer you are responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables.
Role
• 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 CC process.
• Create data programming specifications per specified study requirements.
• Program clinical data programs per specification.
• Validate clinical data programs per the formal, documented CC process.
• 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.
• Review and quality assure CRF annotations produced by other programmers.
• Review and quality assure supporting documentation produced by other programmers.
• 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
• Manage programming and validation activities across a single project, ensuring that timelines are met and deliverables are of sufficient quality.
Requirements
• EU Proven experience in clinical data programming.
• Successfully manage multiple tasks and timelines.
• Demonstrated ability to perform assigned tasks individually.
• Demonstrated 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 o
• Advanced knowledge of the clinical data programming development life cycle, Advanced knowledge of clinical data programming concepts.
• Associate's degree in information systems, science or related discipline or relevant experience required.
Benefits of Working in ICON
Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
What’s Next
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Inside ICONContent type
BlogsPublish date
04/18/2024
Summary
Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis
Teaser label
IndustryContent type
BlogsPublish date
04/18/2024
Summary
Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials
Teaser label
IndustryContent type
BlogsPublish date
04/12/2024
Summary
Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ
Who we are
Similar jobs at ICON
Salary
Location
Germany, Europe, United Kingdom, Switzerland
Department
Medical Affiars & Medical Writing Roles
Location
Any EMEA Location
Germany
Switzerland
UK
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Medical Writing
Job Type
Permanent
Description
Senior Clinical Trial Transparency Associate is in charge of preparing scientific content to be posted on intranet websites (Health Authority, Company) based on source documents, according to defined
Reference
2024-109700
Expiry date
01/01/0001
Author
Natalia RothAuthor
Natalia RothSalary
Location
India, Chennai
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
• Review and process safety events (pre-marketing, post-marketing, medical device and drug) and/or other medically related information per assigned tasks and project specific procedures • Perform revi
Reference
JR118870
Expiry date
01/01/0001
Author
Archana BakkiyarajanAuthor
Archana BakkiyarajanSalary
Location
Ireland, Dublin
Department
Full Service - Corporate Support
Location
Budapest
Dublin
Warsaw
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Human Resources
Job Type
Permanent
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 I
Reference
JR118579
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Location
Osaka
Tokyo
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Contractor
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
Reference
JR119216
Expiry date
01/01/0001
Salary
Location
Taiwan
Department
Clinical Trial Management
Location
Taiwan
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Job Title: Local Trial ManagerWorking location: Home based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment drivin
Reference
2024-110017
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy TangSalary
Location
Taipei
Department
Clinical Monitoring
Location
Taipei
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Senior Clinical Research AssociateWorking Location: Taiwan Home Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environ
Reference
2024-110013
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy Tang