Sanofi Medical Information Writer Job For Life Sciences, Apply Online
Sanofi Medical Information Writer Job For Life Sciences, Apply Online. MSc, PhD job at Sanofi. Interested and eligible applicants can check out all of the details on the same below
Hey guys for those of you who are interested in applying for a Senior Medical Information Writer job opportunity at Sanofi, then check out all of the possible interview questions listed below.
Job Title – Senior Medical Information Writer
Job ID – R2699598
Location –
- Hyderabad
- Mumbai
Our Team:
Sanofi Global Hub is an internal Sanofi resource organization based in India and is set up to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally.
Main responsibilities:
Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues. Achieved through a combination of product knowledge, along with editing
, writing, and document management proficiency.Essential Job duties and responsibilities:
- Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature.
- Generates evidence-based, accurate, current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s).
- Adapts global scientific response documents for assigned countries.
- Develops responses to escalated inquiries for assigned countries.
- Develops contributions to US NDA Annual Reports.
- Contributes to US compendia reviews.
- Contributes to peer reviews.
- Demonstrates resolve and urgency to accomplish tasks without direct authority or control. Participate in cross-functional project teams as needed. Ensure that assigned projects are completed on schedule.
- Develops and maintains Therapeutic Area expertise.
- Reviews the content created by peer writers.
- Collaborates effectively with Global Medical Information teams to execute content plans
- People: 1) Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise.
- Performance: Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality
- Process: 1) Act as an expert in the field of medical information writing and maintain on the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process. 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery.
- Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables.
About you
- Experience: >5 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; At least 2-3 years of direct medical information experience in a pharmaceutical company
- Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment
- Technical skills: As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills, Knowledge about literature evaluation and multilevel response development)
- Education: Advanced degree in life sciences/ pharmacy/ similar discipline, or medical degree or doctorate degree (PharmD, Ph.D, Master in science, MBA or equivalent)
- Languages: Excellent knowledge of the English language (spoken and written)
Hey guys for those of you who are interested in applying for a Senior Medical Information Writer job opportunity at Sanofi, then check out all of the possible interview questions listed below.
- Can you describe your experience with conducting literature searches and reviews? How do you ensure the accuracy and relevance of the extracted data? Answer: In my previous role, I have conducted extensive literature searches and reviews to gather scientific information. To ensure accuracy and relevance, I employ a systematic approach by using keywords and filters, critically evaluating the sources, and considering the study design, sample size, and credibility of the authors. I also cross-reference information from multiple sources to validate the findings and avoid bias.
- How do you develop evidence-based and fair-balanced summaries of data for scientific response documents? Can you provide an example of a challenging situation you faced while creating such content? Answer: To develop evidence-based and fair-balanced summaries, I carefully analyze the data, ensuring that I consider both the positive and negative aspects. I adhere to regulatory guidelines and scientific standards while presenting the information objectively. An example of a challenging situation was when I had to create a scientific response document for a product with limited available data. In such cases, I collaborated with subject matter experts, conducted additional research, and utilized my critical analysis skills to present the available evidence accurately and fairly.
- How do you adapt global scientific response documents for different countries? What factors do you consider during this adaptation process? Answer: When adapting global scientific response documents, I consider several factors such as regulatory requirements, cultural nuances, and regional guidelines. I collaborate with local medical teams and stakeholders to understand the specific needs and preferences of the target country. I ensure that the content is relevant, accurate, and complies with local regulations while maintaining consistency with the global document.
- How do you handle escalated inquiries? Can you describe a situation where you successfully addressed a complex inquiry and provided a comprehensive response? Answer: When handling escalated inquiries, I approach them with a systematic and thorough process. I gather all necessary information, consult internal and external experts if required, and conduct in-depth research to address the complexity of the inquiry. An example of a complex inquiry was when a healthcare professional requested detailed information about potential drug interactions for a specific patient population. I collaborated with the pharmacovigilance department, reviewed available literature, and consulted clinical experts to provide a comprehensive response that included relevant safety considerations and guidance for the healthcare professional.
- How do you ensure the quality and timeliness of deliverables such as scientific response documents and annual reports? Can you provide an example of how you managed multiple projects and met deadlines? Answer: To ensure quality and timeliness, I follow a structured project management approach. I prioritize tasks, create realistic timelines, and communicate with stakeholders to align expectations. I also perform thorough reviews and quality checks before finalizing deliverables. An example of managing multiple projects and meeting deadlines was when I had to simultaneously work on scientific response documents for different therapeutic areas. I effectively utilized time management techniques, delegated tasks when appropriate, and maintained open communication with the team to ensure all projects were completed on schedule without compromising quality.
Note: The answers provided are general guidelines, and it is important to tailor the responses to reflect your specific experience and qualifications for the role.
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