Opportunity for Clinical Research Associate @ 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: Clinical Research Associate
Job Description
The key responsibilities Trainee Clinical Research Associate is to coordinate with regulatory team for HA dossier preparation and submission. To coordinate with local trial manager for EC dossier preparation and submission. To ensure collection and review of green light documents as per NN Sop’s. To plan and conduct site monitoring visits as per the protocol timelines. To review and ensure maintenance of investigator trial files on regular basis. To prepare monitoring reports and upload into IMPACT after review by PM/LTM within specified timelines. To ensure smooth closeout of the study as per guidelines.
Last but not least, acting in line with ethical standards of the organization by personally observing when in the field that we all live with BE policies.
Candidate Profile
You hold Graduate/Post graduate in science, Pharmacy or Medical. Additional qualification in clinical research would be preferred. Minimum 1 year experience trainee CRA or 1-2 years of experience in clinical research in a CRO or a Pharma company.
You have excellent communication & influencing skills and can drive projects and processes.
You are fluent in both written and spoken English.
Additional Information:
Experience: 1-2 Years
Qualification: B.Pharm, B.Sc, M.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Location: Bangalore- Karnataka
Requisition ID 29677BR
Last date: 10th June, 2015
Click here to apply
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: Clinical Research Associate
Job Description
The key responsibilities Trainee Clinical Research Associate is to coordinate with regulatory team for HA dossier preparation and submission. To coordinate with local trial manager for EC dossier preparation and submission. To ensure collection and review of green light documents as per NN Sop’s. To plan and conduct site monitoring visits as per the protocol timelines. To review and ensure maintenance of investigator trial files on regular basis. To prepare monitoring reports and upload into IMPACT after review by PM/LTM within specified timelines. To ensure smooth closeout of the study as per guidelines.
Last but not least, acting in line with ethical standards of the organization by personally observing when in the field that we all live with BE policies.
Candidate Profile
You hold Graduate/Post graduate in science, Pharmacy or Medical. Additional qualification in clinical research would be preferred. Minimum 1 year experience trainee CRA or 1-2 years of experience in clinical research in a CRO or a Pharma company.
You have excellent communication & influencing skills and can drive projects and processes.
You are fluent in both written and spoken English.
Additional Information:
Experience: 1-2 Years
Qualification: B.Pharm, B.Sc, M.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Location: Bangalore- Karnataka
Requisition ID 29677BR
Last date: 10th June, 2015
Click here to apply
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