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Novotech hiring Clinical Data Programmer Trainee. Pharmacy or Clinical Research or life science related field or similar. Eligible

 Novotech hiring Clinical Data Programmer Trainee.. Pharmacy or Clinical Research or life science related field or similar eligible 








Brief Position Description:



The core responsibility for this position is as a member of the Data Management SAS department at Novotech. The Clinical Data Programmer SAS Trainee (CDP-ST) will be responsible for performing SAS programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).


Minimum Qualifications & Experience:



Graduate in Information Technology or Pharmacy or Clinical Research or life science related field or similar. Base SAS Certified with good understanding of Clinical Research terminologies. Awareness about different electronic data capture tools and metadata would be an added advantage. 


Responsibilities:


• The Clinical Data Programmer SAS Trainee will be responsible for SAS programming activities on different projects across different EDC applications in accordance with Novotech standards.

• Perform programming and QC of SAS programs for data listings or reconciliation listings or patient profiles or any other tables/graphs as per specifications for the Data Management group.


• The Clinical Data Programmer SAS Trainee may be requested to design eCRFs and edit checks after necessary training for the respective EDC tools and provide technical support on projects.


• Perform data mapping/reconciliation specifications and programming per the for the respective project. This will also include alpha testing before releasing.


 


 Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.


JOB-DETAILS.EMPLOYER-DESCRIPTION-TITLE

Novotech has offices in 11 geographies across the region, and site partnerships with key medical institutions.


Novotech provides clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management. Novotech obtained the ISO 27001 certification which is the best-known standard in the ISO family providing requirements for an Information Security Management System. Together with the ISO 9001 Quality Management system, Novotech aims at the highest IT security and quality standards for patients and biotechnology companies.

JOB-DETAILS.ORGANIZATION-DESCRIPTION-TITLE

Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services.


It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. Novotech is positioned to serve biopharmaceutical clients conducting clinical trials in Asia and globally.


As of September 30, 2021, Novotech had over 2,750 FTEs across 11 geographies in Asia-Pacific, the United States and the UK.




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