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Clinical Data Programmer

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 III you are responsible for specifying, developing, validating and executing programs and generation of clinical data deliverables. The Clinical Data Programmer Ill is additionally responsible for QC of junior programmer deliverables and assisting with project management activities.
 

JOB FUNCTIONS/RESPONSIBILITIES:

·         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, .

·         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 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 req

 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

- See more at: http://careers.iconplc.com/job/clinical-data-programmer-i-jobid-010665_2#sthash.udYHwMo3.dpuf

Job Posted by

·         Company:iconplc

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies. In a highly fragmented industry, we are one of a small group of organisations with the capability and expertise to conduct clinical trials and development projects on either a local or global basis. We have the operational flexibility to provide development services on a stand-alone basis or as part of an integrated full service solution.