Clinical Data Programmer Ii

2 weeks ago

Bengaluru, India Novotech Asia Full time

**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).

**Minimum Qualifications & Experience**

Graduate in information science or life science related field, or similar. Two years experience in a similar role in a CRO or pharmaceutical company.

**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.
- 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.
- Ability to learn new process, programming languages and adapt with new technologies

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.

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