PhD Lifescience Healthcare Job New

PhD Lifescience Healthcare Job – Apply Online

PhD Lifescience Healthcare Job – Apply Online. Novartis purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. Please find the below-given job details of the PhD Lifescience Healthcare Job. You can go through the details and apply online.

Position – Senior Medical Information Manager I

Location – Hyderabad #LI Hybrid

About the Role:

To be responsible for delivering sophisticated and highly sophisticated Medical Information (MI) activities, and for providing functional and therapeutic area/brand expertise to support responses to escalated medical enquiries on established brands from Novartis country affiliates worldwide.

Key Responsibilities:

  • Responsible for delivery of sophisticated and highly complex MI activities, including new Global guidance Documents for priority/launch brands.
  • Provide timely and quality responses to medical enquiries raised from Novartis country affiliates for established brands. Ensure adherence to critical metrics with regard to timeliness, and meet the minimum criteria in quality reviews conducted by management
  • Write and review MI results such as global guidance Documents (GGDs), MI Q&As to ensure they meet quality requirements – scientifically balanced and evidence-based, adhere to topic/key messages, language and grammar are accurate, regulatory/safety/legal aspects are considered.
  • Provide input into MI Service processes and standards to ensure optimal efficiency and productivity.
  • Contribute to the generation of reports for partners (SSP management, relevant Division management, Franchise and Brand teams) on enquiry metrics and insights from countries and regions.
  • Write (or review) highly complex MI services which require the experience and expertise of a Senior MI Manager. This can include services with a mixed model, with the Senior MI Manager working alongside the MI Manager.

Minimum requirements for PhD Lifescience Healthcare Job-

Essential Requirements:

  • Minimum 2 years’ experience in Medical Information/Communications in the Pharmaceutical Industry (or related Medical Affairs role).
  • Knowledge and application of good practices in medical enquiry management and writing for medical information.
  • Proven understanding of medical concepts and the implications on a broader scale in the Pharmaceutical industry (regulatory, PV, legal, commercial, drug development, etc.)
  • Strong cross-functional skills and proven experience in collaboration with other departments/groups.

Desirable Requirements:

University degree in PhD, PharmD, MD) in life science/healthcare.


Prepare to excel in your upcoming interview using the questions and answers we’ve provided. Study these to craft effective responses and stand out during the interview for PhD Lifescience Healthcare Job. Best of luck! We’re here to help you succeed!

Question 1: Can you provide an example of a highly complex Medical Information activity you’ve managed, including the challenges faced and how you addressed them? Answer: Certainly. In my previous role, we received a surge of medical enquiries about a priority brand. The challenge was to provide accurate and detailed responses within tight timelines. I collaborated with cross-functional teams to streamline the process, prioritize enquiries, and ensured that the responses were evidence-based, scientifically balanced, and aligned with regulatory guidelines. This approach improved efficiency and maintained the quality of responses.

Question 2: How do you ensure that your medical information responses are not only accurate and scientifically sound but also aligned with regulatory and legal considerations? Answer: Ensuring accuracy and compliance in medical information is crucial. I thoroughly research each enquiry, referencing up-to-date scientific literature, guidelines, and regulatory documents. Additionally, I collaborate closely with regulatory and legal teams to ensure that responses align with current regulations and safety requirements while effectively communicating the necessary information to the requester.

Question 3: Can you share an instance when you had to write or review Global Guidance Documents (GGDs) or Medical Information Q&As? How did you ensure that they met quality standards and conveyed complex medical concepts clearly? Answer: Certainly. I recently led a team in crafting GGDs for a new launch brand. To maintain quality, I ensured that the documents were evidence-based and scientifically accurate. I worked with subject matter experts to ensure clarity in conveying complex medical concepts. Furthermore, I conducted rigorous reviews for grammar, language, and adherence to key messages, ensuring that the content was consistent and met regulatory and medical communication standards.

Question 4: Collaboration is crucial in a role like this. Can you provide an example of a successful cross-functional collaboration that improved the efficiency of your medical information services? Answer: Absolutely. In a previous project, I collaborated with the Pharmacovigilance team to enhance the process of adverse event reporting in medical information responses. By aligning our procedures and sharing relevant data, we streamlined the reporting process, ensuring timely and accurate communication of safety information. This collaboration not only improved efficiency but also enhanced patient safety.

Question 5: How do you stay updated on the latest medical and regulatory developments in the pharmaceutical industry to ensure your medical information responses are current and accurate? Answer: Staying informed is essential. I regularly participate in medical conferences, webinars, and workshops. I also subscribe to reputable medical journals and regulatory updates to stay current with industry trends. Additionally, I actively engage with internal and external experts to exchange knowledge and insights, ensuring that my responses are evidence-based and aligned with the latest developments.

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