Clinical and Safety Publisher

Job title: Clinical and Safety Publisher

Company: Novo Nordisk

Job description: By continuing to use and navigate this website, you are agreeing to the use of cookies.
Accept Close

Press Tab to Move to Skip to Content Link

Search by Keyword

Loading…

Category

Search by Location

×

Select how often (in days) to receive an alert:

×

Select how often (in days) to receive an alert:

Clinical and Safety Publisher

Category: Clinical Development and Medical

Location:

Bangalore, Karnataka, IN

Department- Clinical Reporting, GD-GBS

Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment and support your colleagues and stakeholders by challenging the status quo in a friendly and open-minded way? If so, there is a job opportunity waiting for you as our new Clinical Publisher. At Novo Nordisk, we will challenge you to do the best work of your life. Apply Now.

The Position:

Clinical Publisher will be responsible for Compilation and publishing of clinical documents including but not limited to Clinical Trial Reports (CTRs), Investigator’s Brochures (IB), Non-intervention Study Reports (NSRs), Clinical summaries and overviews, lay summaries etc. Plan and coordinate the collection of appendix material in collaboration with the medical writer, study group and local affiliates. Check appendix documentation and ensure adherence to internal and regulatory publishing standards (e.g., regarding navigation, bookmarks, hyperlinks, margins, header).

Support clinical users and troubleshoot issues related to the clinical templates. Perform eCTD checks of reports including but not limited to Non-clinical CRO Reports, Non-clinical Section Reports for Clinical Trial Reports, Non-clinical Principal Investigators Reports, Clinical CRO Reports for Clinical Trial Reports etc according to internal PDF check list. Contribute and conduct knowledge sharing sessions and sharing better practices in the team.

Qualifications:

  • Post-graduate (Pharmacy, Science, IT, Engineering) or relevant bachelor’s degree.
  • 2+ years of relevant experience in the routine use of Document Management Systems, MS Office, Portable Document Format (PDF) tools including Adobe Acrobat Professional and ISI toolbox.
  • General knowledge and understanding of FDA, ICH, and other regulatory electronic documentation requirements.
  • Good team player with communication and stakeholder management skills.

About the Department

The Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6-7 years, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled Medical Writers, Disclosure Medical Writers, Publishers and Document Controllers with Masters/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge on different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7-8 years in writing and reviewing regulatory documents and publications. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. Apart from writing and publishing regulatory documents, the team is also responsible for distribution of documents (CONNECT portal) and largely contributes to NN’s regulatory commitments by being involved in public disclosure activities.

Working at Novo Nordisk

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.

Contact

  • To submit your application, please upload your CV online (click on Apply and follow the instructions).

Deadline

Apply before 10th November, 2022.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Expected salary:

Location: Bangalore, Karnataka

Job date: Thu, 03 Nov 2022 23:55:39 GMT

Apply for the job now!