Brief Position Description:
The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).
Responsibilities :
- The CDP-II shall be responsible for programming activities on a project. This shall include designing and implementation of clinical database, programming of data review listings and programming of data reconciliation. The CDP-II shall ensure quality standards per SOPs and ICH-GCP.
- Participates in project team meetings as required.
- The CDP-II shall be responsible for designing, programming, testing and maintenance of clinical trial databases in different clinical trial applications in accordance with Novotech standards.
- Perform external data loads, i.e. labs, ECGs etc., as needed. Act as liaison with vendors to establish data transfer specifications standards.
- Ensure all programming activities and processes performed are conducted in accordance with standard operating procedures and good programming practices.
- Experience in developing, validating and maintaining clinical trials built in different EDC applications.
- Ability to learn new process, programming languages and adapt with new technologies.
- Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
- To have the technical knowledge and provide guidance on providing interfaces or data exchanges between the clinical database and other database, programming or reporting systems.
- Support in the validation of electronic systems, software and programs implemented in accordance with current regulatory requirements.
- Support on project meetings and telephone conferences where required. The CDP shall support the Project Lead on a project on tasks as needed.
Requirements :
- Graduate in information science or life science related field, or similar.
- Two years experience in a similar role in a CRO or pharmaceutical company.
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 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 talking to you about working at Novotech.
ResponsibilitiesResponsibilities for Clinical Data Programmer-II at NovotechThe CDP-II shall be responsible for programming activities on a project. This shall include designing and implementation of clinical database, programming of data review listings and programming of data reconciliation. The CDP-II shall ensure quality standards per SOPs and ICH-GCP.
Participates in project team meetings as required.
- The CDP-II shall be responsible for designing, programming, testing and maintenance of clinical trial databases in different clinical trial applications in accordance with Novotech standards.
- Perform external data loads, i.e. labs, ECGs etc., as needed. Act as liaison with vendors to establish data transfer specifications standards.
- Ensure all programming activities and processes performed are conducted in accordance with standard operating procedures and good programming practices.
- Experience in developing, validating and maintaining clinical trials built in different EDC applications.
- Ability to learn new process, programming languages and adapt with new technologies.
- Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
- To have the technical knowledge and provide guidance on providing interfaces or data exchanges between the clinical database and other database, programming or reporting systems.
- Support in the validation of electronic systems, software and programs implemented in accordance with current regulatory requirements.
- Support on project meetings and telephone conferences where required. The CDP shall support the Project Lead on a project on tasks as needed.
Graduate in information science or life science related field, or similar.
Two years experience in a similar role in a CRO or pharmaceutical company.
About UsNovotech is a global full-service clinical Contract Research Organization (CRO).
At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition, innovation, and growth. Named Employer of Choice, Great Place to Work and Employer of Choice for Gender Equality (EOCGE), we are committed to fostering an environment that reflects the life-changing work we do.
Since 1997, we have expanded our global footprint, now with 30+ offices across Asia-Pacific, the United States, and Europe. This growing network unites professionals from diverse backgrounds and disciplines to advance therapies that improve patient outcomes worldwide.
At Novotech, our employees are at the heart of our success. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.
With access to mentorship opportunities, professional development programs, and a dynamic community, Novotech offers a platform for driven individuals to achieve personal growth while shaping the future of healthcare. Join us to be a part of a team that values your contributions and supports your ambition to make a global impact.
At Novotech we have advanced therapeutic and regulatory expertise, the ability to execute across markets and a client-centric service model, so that our clients get a trusted, long-term partner and an accelerated path to bring their life-changing advances to market. This gives our employees the opportunity to develop their careers by joining a diverse and supportive global organization with a collaborative culture, whilst working with clients on the cutting-edge of life sciences.
At Novotech you will work alongside empowered teams with a shared commitment to success.
- Strategic vs transactional mindset.
- Ability to gain insights and make proactive decisions quickly.
- Culture that fosters partnership and collaboration, where every voice is heard and valued.
- Ongoing support from senior stakeholders and leadership team.
Skills Required
- Graduate degree in information science, life science, or a similar field
- Two years of experience in a similar role at a CRO or pharmaceutical company
What We Do
Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, "Novotech" and "PPC". Novotech is a full-service clinical CRO with labs, phase I facilities, and drug development consulting services.
