Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).
Post: Associate Trial Data Programmer
Job Description
- Ensuring the integrity of clinical trial databases
- Handle all trial execution related to CDMS with regard to programming and UAT
- Understand and comply with all applicable standard operating procedures and working instructions
- Develop and maintain good communications and working relationships with Data Management team
- Data entry screens and validation/derivation procedures should be built as per trial-specific standards and abiding to project
- The Associate Trial Data Programmer should have attention on irregularities, deviations and should therefore arrive for the probable solutions for the foreseen risks and thus to decide on the relevant proposals for actions.
- Has basic programming skills to understand database tables and relationships between different tables, Can create views in OC
- Should be able to extract raw data listings as required and be able to use novoDOCS
- Experienced in one of MS office application and capable of using the whole MS office suite.
Candidate Profile
M.Sc / B.Sc in Life Science or comparable degree in computer science, Information Technology clinical information management or equivalent qualifications.
Minimum 1-2 yrs in Trial Setup and Programming in Oracle Clinical is mandatory. Good knowledge on SQL and PL-SQL..
Note: Freshers need not apply
Additional Information:
Experience: 1-2 Years
Qualification: B.Sc, M.Sc in life sciences
Location: Bangalore- Karnataka
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Other
End Date: 30th April, 2015
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