Clinical Data Programmer III Post in ICON in Chennai
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
• Recognize, exemplify and adhere to ICON's values which centers 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.
• Travel (approximately 0%) domestic and/or international
• *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 data set and programming specifications produced by otner 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 & sponsos 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.
• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions,
• USILATAM/CAN, At least 4 years prior experience in clinical data programming.
• EU/APAC: 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
• 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.
Location: Chennai
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 22nd Sep, 2013
For more Jobs visit Jobes Mantra
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
Post: Clinical Data Programmer III - 005435
Job Description
• Recognize, exemplify and adhere to ICON's values which centers 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.
• Travel (approximately 0%) domestic and/or international
• *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 data set and programming specifications produced by otner 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 & sponsos 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.
QUALIFICATIONS/EXPERIENCE REQUIRED:
• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions,
• USILATAM/CAN, At least 4 years prior experience in clinical data programming.
• EU/APAC: 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
• 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.
Additional Information:
Location: Chennai
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 22nd Sep, 2013
For more Jobs visit Jobes Mantra
Kindly Share This Job With Yours Friends.
0 comments:
Post a Comment