2.0 - 6.0 years

0 Lacs

maharashtra

On-site

As a Medical Advisor at Novartis, you will play a crucial role in supporting the design, implementation, and execution of Medical Affairs plans for the assigned Therapy Area. Your responsibilities will include coordinating scientific meetings, symposia, and congresses, as well as engaging in Continuous Medical Education (CME) activities. You will work towards providing scientific information, designing and organizing clinical studies, and fostering educational dialogues with Key Opinion Leaders (KOLs) and regulatory stakeholders. Your essential requirements for this role include holding an MBBS or MD degree with a minimum of 2+ years of industry experience. You should have expertise in Operations Management, Project Management, Clinical Trial Design, Medical Science, Disease Area Knowledge, Medical Education, and Scientific Engagement. Additionally, experience in Non-Interventional Studies (NIS) and Epidemiology Studies will be beneficial. Desirable requirements include experience in Ophthalmology and/or Immunology. In this position, you will support the country medical affairs strategy in alignment with the global strategy, country insights, and market conditions. You will be responsible for coordinating the review and approval of medical materials, ensuring compliance, and tailoring global materials to local needs. Furthermore, you will provide medical insights to various cross-functional groups and contribute to risk identification, assessment, and mitigation planning. Novartis is dedicated to reimagining medicine to improve and extend people's lives, aiming to become the most valued and trusted medicines company globally. By joining Novartis, you will be part of a mission-driven organization that values its associates and strives to achieve ambitious goals. If you are passionate about making a difference in healthcare and collaborating with a diverse team, this opportunity may be the perfect fit for you. To explore more about Novartis and its commitment to diversity and inclusion, visit: https://www.novartis.com/about/strategy/people-and-culture. Additionally, you can learn about the benefits and rewards offered by Novartis in the Novartis Life Handbook: https://www.novartis.com/careers/benefits-rewards. Novartis is committed to fostering an inclusive work environment and building diverse teams that reflect the patients and communities it serves. If you require any accommodations due to a medical condition or disability during the recruitment process, please reach out to [email protected] with your request and contact information, mentioning the job requisition number in your message. Join the Novartis Network to stay connected and learn about future career opportunities and advancements within the organization: https://talentnetwork.novartis.com/network. Your dedication and expertise can contribute to creating a brighter future for patients and communities worldwide.,

Posted 6 days ago

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Medical Device Safety Physician Gratitude India

3.0 - 7.0 years

14 - 16 Lacs

Pune, Chennai, Mumbai (All Areas)

Work from Office

Medical Device Safety Physician – MBBS/MD mandatory. Review medical device safety reports (ICSR, SUSAR), assess risks, and ensure MDR/EU/US compliance. PV, clinical trials experience required. Required Candidate profile Strong decision-making, regulatory knowledge. WFO (Mumbai/Gandhinagar/Chennai/Pune/Indore). Salary up to 16 LPA.

Posted 3 weeks ago

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Medical Reviewer Fresenius Kabi

1.0 - 6.0 years

10 - 15 Lacs

Gurugram

Work from Office

We are looking for MBBS - Medical Reviewer with 2-3 years of experience in Pharmacovigilance having expertise in review f aggregate reports. Candidate who are willing to come to office and work from office only can apply. Designation : Asst. Manager Department : Vigilance Competence Center Gurgaon, Qualification : MBBS/MD with 2-3 years of experience in pharmacovigilance with expertise in medical review of aggregate reports (PSURs/PBRERs) (required), with experience in performing medical review of signal management and ICSRs (recommended). Location : Gurgaon (Work from office is must with one-day flexi working option) Job Responsibility Design, develop and maintain procedures for medical review activities (ICSRs, aggregate reports and signal management). Ensure high quality of ICSR, aggregate and signal management deliverables. Perform medical review of ICSRs, aggregate reports (PSURs/PBRERs), Risk Management plans, and signal reports. Participate in/organize review of safety label updates. Mentor and train medical reviewers. Provide product and therapeutic area trainings for the PV team. Provide cross-functional training on pharmacovigilance to medical writing and ICSR team members. Behavioral Competencies Excellent interpersonal communication and writing skills with experience handling cross-functional projects Good conflict resolution skills Ability to work in a multi-cultural/global work environment Good mentoring skill

Posted 3 weeks ago

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