Opening for Clinical Research / Life science / Pharmacy candidates for the post of Clinical Research Associate @ Novo Nordisk
Novo Nordisk is a global healthcare company with 90 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 39,000 employees in 75 countries, and markets its products in more than 180 countries.
Job Title : Clinical Research Associate
Eligibility : B.sc/M.sc Clinical research / Life science/ B.pharma/ M.pharma
Experience : 1-2 years
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.
Click here to apply
Novo Nordisk is a global healthcare company with 90 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 39,000 employees in 75 countries, and markets its products in more than 180 countries.
Job Title : Clinical Research Associate
Eligibility : B.sc/M.sc Clinical research / Life science/ B.pharma/ M.pharma
Experience : 1-2 years
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.
Click here to apply
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