Senior Clinical Data Programmer
vor 1 Woche
Add expected salary to your profile for insights.
The SCDP acts as primary point of contact for project team members to address and resolve issues at technical and DB development level.
They are also responsible for providing technical and development leadership across multiple projects assigned to the CDP team members ensuring that they deliver in accordance with the requirements.
Responsibilities Participate in Client and Project meetings as required to explain the CDP requirements, process and throughput times.Undertake troubleshooting and resolution of any technical issues.
Liaise with data management, statistical and clinical teams to ensure efficient operations and problem resolution.Liaise with internal Biometrics specialized teams to resolve issues affecting timely completion of CDP deliverables.
Escalate issues to Manager CDP and Director CDP, as required.Undertake advanced programming/custom functions for study DB edit checks and configuration and development of other system requirements.Undertake quality and technical reviews of team members' critical CDP deliverables as part of database builds, database migrations, database lock and database decommissioning activities, as well as CDP filing of critical documentation required in the TMF.Undertake technical scoping and impact analysis for system changes and migrations.Review validation results and undertake development fixes.
Proactively identify and communicate risk and database update requirements.Minimum Qualifications & Experience: Graduate in information science or life science related field, or similar.More than five years' experience in a Senior Clinical Data Programmer role in a pharmaceutical company, CRO or EDC software provider, including supervision and training of other programmers.Extensive programming experience in different EDC tools e.g., Medidata Rave, Viedoc, Veeva and associated modules like RTSM, ePRO is preferred.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 one 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 in 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.
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Headquartered in Australia and focused exclusively on the Asia Pacific, Novotech is internationally recognized as a leading regional full-service CRO.
With the increasing pace of globalization in drug development, Novotech's expertise in the vibrant and fast growing Asian region has been instrumental in the success of hundreds of phase I-IV clinical trials from Australia to India.
Headquartered in Sydney, with operations in New Zealand, China, Hong Kong, India, Malaysia, the Philippines, Singapore, South Africa, South Korea, Taiwan and Thailand, Novotech's service offering has come to be recognized for its quality both by our clients, as well as industry analyst groups.
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