Novo Nordisk B Pharma Job Opening 2022 – Apply Online
Novo Nordisk Hiring Pharma candidates. B Pharma job opening 2022. Pharma job opening 2022.Project Manager job opening 2022. Candidates with bachelor’s degree in pharmacy may apply for the job opening at Novo Nordisk. Pharmacy job opening 2022. Check out all the details on the same below:
Does your motivation come from challenges and working in a dynamic environment? Is your ambition to create visible results? Are you enthusiastic about understanding the Clinical Operations and bringing attention to key project management challenges? Then you might have the right position for you.
Job Title: Project Manager
Category: Clinical Development and Medical
Location: Bangalore, Karnataka, IN
Eligbility Criteria:
- You should have a bachelor’s degree in pharmacy, nursing qualification, or equivalent.
- You should have least 5+ years of experience in clinical monitoring.
- Basic GCP qualification and high level of understanding of GCP requirements.
- You must have advanced-level knowledge of Excel and PowerPoint presentations.
- Good working knowledge of electronic clinical trials systems – IMPACT, EDC, IWRS, electronic TMF.
- Good Communication and should be able to collaborate with internal and external stakeholders.
The position
Project Manager is the main person accountable in making sure that deliverables
are met as per project timelines, within budget and complying with Protocol, country regulatory requirements, Helsinki Declaration, GCP (Good Clinical Practice) and NN SOPs (Standard Operating Procedures).You will be responsible for –
- Driving assigned clinical trial from the feasibility to Clinical trial reporting. The activities include planning, site selection, Ethics committee and health authority submissions, starting-up trial sites, organize investigator meetings.
- Training Site staff, CRAs, CTAs, and start-up teams about the protocol and other protocol-related information, providing operational and therapeutic expertise to the CDC project team, achieving deliverables within agreed timelines and in accordance with scientific, quality, and regulatory requirements and ensuring effective communication of all trial/project related issues between HQ, CDC, the region, and other Internal/external stakeholders.
- Responsible for representing CDC countries in relevant study meetings and organize these meetings: Trial Squad Meetings Monitor meetings, Investigator meetings, Study Result meetings.
- All trial-related documents review and customizations as relevant, coordinate contract finalization process as decided by the country legal responsible.
- Ensure all the sites are activated as early as possible. Escalate any projected delay to the clinical operations manager and/or CDC Head and also ensure all the sites are audit and inspection ready.
Apply Online
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