Job in RIMS Data Management as Associate at Novo Nordisk

Novo nordisk's data management department was established in Bangalore, India in the month of September 2007 and has significantly grown from 10 members to a strong team of over 140 Clinical Data Management professionals. It has witnessed significant transformations right from providing DM services to IO region reporting to IOCDC to becoming an integral part of Global development from Aug 2010. It is a young, enthusiastic and dynamic team with varied skillsets and professionals from diverse backgrounds such as pharmacy, life-sciences, physiotherapy, computer / information sciences and business administration.

Post : Associate - RIMS Data Management

Job Description
You will be responsible for RIMS jobs, RIMS executed forms archival into Documentum system, RIMS Data Entry for Regulatory changes & updates and ensure high quality in data entry in accordance with defined KPI's and SOP’s and internal guidelines/policies; daily maintenance and control of data in RIMS system and securing quality of existing data. Continuous collaboration with RAHQ DK and RA in business regions through mails, tele conferences etc. , do follow-ups and record the internal work flow data into internal data tracking system, to enable the jobs traceability, KPI Reports etc., as per the procedures. Work as per targets and timelines, support the team as per business requirements & be a good team player, able to understand required process quickly, actively involved in cross functional activities, responsible for sharing better practices, responsible for own continuous development.   Daily operational business has to comply with defined KPIs and SOPs. There is a limited degree of independence; however as innovation is critical in respect to LEAN including continuous improvement, you are expected to be proactive and take an active part in the daily operations.


Candidate Profile
Relevant academic degree at minimum bachelor level e.g. Graduation in Science, Pharmacy/computer science. Professional skills include Data Entry & Data Management, Knowledge in Regulatory Affairs, Regulatory Affairs Documentation, and Knowledge in Register Database preferred; Above 1 year relevant work experience, strong skills on service culture and delivery.  Proficiency in oral and written English is essential together with a high degree of integrity.

Additional Information:
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
Requisition ID: 47808BR
End Date: 10th July,  2017

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