Sanofi is hiring Associate Project Specialist- HEVA opening 2023 for Medical communication or pharma experience candidates, Interested and eligible candidates may check out all the details on the same below
Job Title: Associate Project Specialist-HEVA
Job Location: Hyderabad
Job type: Full time
About the job:
Our Team: Sanofi Global Hub (SGH) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Med Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.
Main responsibilities for Latest Associate Project Specialist at Sanofi:
Qualification we seek in You for Latest Associate Project Specialist at Sanofi:
- Experience: Medical communication/pharma experience desirable. Project management experience required. 1-3 years post qualification experience. Project management/medical communication/pharma experience desirable.
- Soft skills: Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment
- Technical skills: As applicable (including but not limited to therapeutic area/domain knowledge exposure; publication submission; and/or project management)
- Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree
- Languages: Excellent knowledge of English language (spoken and written)
Possible Interview Questions for Latest Associate Project Specialist at Sanofi:
- Can you describe your experience in medical communication or the pharmaceutical industry?
Answer: I have a [X years] of experience in medical communication/pharmaceutical industry. In my previous roles, I have worked on various projects involving medical writing, creating scientific content, and collaborating with cross-functional teams. I have a solid understanding of healthcare regulations, industry guidelines, and the importance of clear and accurate communication in disseminating scientific information.
2. How do you approach managing multiple projects and meeting deadlines?
Answer: I believe in effective project management techniques such as creating detailed project plans, setting clear priorities, and regularly monitoring progress. I also emphasize open communication and collaboration with team members to ensure everyone is aligned and aware of project timelines. Additionally, I am adept at identifying potential bottlenecks or challenges and proactively addressing them to ensure timely delivery of projects.
3. Can you provide an example of a challenging project you have worked on and how you handled it?
Answer: In my previous role, I was involved in a complex medical communication project that required extensive coordination between multiple stakeholders, tight timelines, and a large volume of scientific data. To handle this, I established regular meetings with the team to ensure clear communication and alignment. I also broke down the project into smaller tasks, assigned responsibilities, and closely monitored progress. By prioritizing effectively and leveraging strong organizational skills, I successfully delivered the project on time.
4. How do you stay updated with the latest advancements in medical communication or the pharmaceutical industry?
Answer: I am committed to continuous learning and professional development. I regularly attend conferences, workshops, and webinars related to medical communication and the pharmaceutical industry. I actively follow reputable scientific journals, industry publications, and online resources to stay abreast of the latest research, regulatory updates, and best practices. I believe in networking and collaborating with industry professionals to exchange knowledge and insights.
5. How do you ensure accuracy and compliance in your work within the medical communication or pharmaceutical field?
Answer: Accuracy and compliance are paramount in the medical communication and pharmaceutical field. I pay meticulous attention to detail and ensure that my work aligns with the relevant guidelines, regulations, and internal quality standards. I am well-versed in the International Committee of Medical Journal Editors (ICMJE) guidelines, Good Publication Practice (GPP), and other industry-specific guidelines. I also utilize thorough review processes, peer feedback, and quality control measures to ensure accuracy and compliance in all my deliverables.