Inviting Junior Safety Associate in Novo Nordisk

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: Junior Safety Associate

Job Description
Novo Nordisk is one of the world’s most successful pharmaceutical companies and with a great growth potential. Do you want to be part of this?

The role entails to perform initial evaluation and data entry of all serious and non-serious adverse events (SAEs). Data entry and coding of adverse events from spontaneous post marketed reports, clinical trials phase 1-4 based on individual case histories, correspondence with affiliates, other departments and various administrative assignments. Data verification between source data and Argus database. Ensure accurate and consistent coding of all events entered in Argus with the use of MedDRA (Medical Dictionary for Regulatory Activities). Evaluate seriousness, causality and listedness. Assess the need for follow up information and issue or draft follow up requests, as applicable. Archiving of cases in Argus

In addition, assist with related administrative and procedural activities as required or requested. Ensure that all tasks are performed in compliance in accordance to GCP/GMP/GXP requirements.

Qualifications
Only Graduates or Post graduates in the field of medicine, dentistry, nursing, pharmacy, homeopathy, unani, Ayurveda and physiotherapy are required to post their resumes. In case you send a non-relevant resume, the resume will be automatically rejected and such candidates will not be able to re-apply for any future positions at Novo Nordisk A/S for the next 6 months.

You have a working knowledge of MS Windows applications including MS Office tools. Excellent written and spoken English. Solid Novo Nordisk organizational or pharmaceutical company understanding. Knowledge of medicinal terminology and clinical pharmacology Knowledge of basic and advanced GCP (Good Clinical Practice) Knowledge of basic and advanced GMP (Good Manufacturing Practice)

You are diligent and have an eye for detail. You show a high level of flexibility and you have excellent communication and cooperation skills. Furthermore, you have a good sense of humour.

We invest a lot in both professional and personal development and have a thorough individualised development plan for each employee. As part of your job you will receive intensive training in Pharmacovigilance.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Additional Information:
Requisition ID: 15692BR
Education: graduates, Post graduates
Industry Type: Pharma/ Biotech/Clinical Research
End Date: 31^st Aug, 2013