Latest job position for Associate Medical Manager in pfizer, Interested and Eligible candidates can check out all the details in the same below.
Job title: Associate Medical Manager
Job Location: India – Remote
Job type: Full time
 JOB MAIN REPONSIBILITIES / DUTIES:
Responsible for providing support to Global Medical Excellence & Innovation (GME&I), Global Technology & Engineering (GT&E), Worldwide Safety and Regulatory teams, specifically:
Author high quality deliverables to support combination product post-production periodic review and activities associated with the maintenance phase of combination products.
Coordinate/assemble information which may be sourced cross functionally.
Perform literature searches in major databases (PubMed/EMBASE) followed by relevancy check and analysis of relevant data.
Evaluate competitive landscape and on a periodic basis analyze changes to the state-of-the-art.
Review the applicable processes, analyze and complete the following inputs:
- Design Changes
- Commitment Tracking (CT) Records
- Competitor information
- Corrective and Preventive Action (CAPA)
- Supplier Corrective Action Request (SCAR)
- Complaint Trends review by product with a deep-dive into Device Engineering Investigation data
- Market Actions
- Perform Risk Management File reviews as part of Post-Production Combination product review.
The Associate Medical Manager supports and partners with cross functional stakeholders including GT&E, Quality, Safety, Regulatory, and Global Medical Affairs by:
- Providing support on assigned tasks for the combination products.
- Assessing document requirements, gauging document complexity, and identifying information gaps or other potential issues. In collaboration with the GT&E Lead, the author proposes or contributes to strategies to resolve any identified issues.
- Ensure clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
- To work collaboratively with team members and to align with agreed timelines. Effectively manage own time and workload.
- Deliver assigned documents on or before deadline, alerting project teams in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality.
REQUIRED SKILL SET:
Technical:
- Regulatory knowledge: Familiarity with global regulatory guidance especially:
- International Conference on Harmonisation (ICH), Food and Drug Administration (FDA) and European Medicines Agency (EMA)
- AAMI TIR105 Risk management guidance for combination products
ISO 13485:2016 Medical Devices-Quality Management Systems—Requirements for - Regulatory Purposes
- US Food and Drug Administration (FDA) regulations published in 21 CFR part 820.30
ISO 14971:2019 Medical Devices-Application of Risk Management to Medical Devices
ISO/TR 24971:2020 Medical Devices-Guidance on the Application of ISO 14971 - Writing skills: Excellent scientific writing skills, including an ability to summarize and interpret complicated data effectively, concisely and persuasively.
- Analytic skills: Utilize tools such as OvidSP and other bibliographic databases such as PubMed, Embase, and Biosis. Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them.
- Language skills: High fluency in written English and strong functional fluency in spoken English.
- Personal skills: Strong organizational skills and ability to prioritize multiple projects and meet deadlines.
- Interpersonal skills: Effective influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy. Ability to work well with all levels and roles in cross-functional, global teams.
- Software: Previous experience with software commonly used to present and analyze data and experience with searching academic databases. (Word, PowerPoint, Excel) is preferred.
Managerial: Reports directly to the Senior Medical Manager. Works closely with GT&E and Quality team colleagues at regional and global level. - Certifications: NA
Qualifications we seek in you!:
Graduate/Post-graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences/Biomedical Engineering or equivalent degrees.
Experience for Associate Medical Manager in pfizer:
- Medical writing experience in the medical devices and/or combination products domain is mandatory.
- 3 years relevant experience for medical graduates and PhDs; 5 years relevant experience for science graduates/biomedical engineers. Minimum 3 years of experience in medical writing within an agency, CRO, Pharma / Biotech Company.
- Prior experience in using search tools, developing search strings and assessing search results is preferred.
- Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Possible Interview Questions may be asked for Associate Medical Manager in pfizer
- Can you tell us about your experience in medical affairs and your understanding of the role of an Associate Medical Manager?
Answer: In my previous role as a Medical Affairs Associate, I gained valuable experience in supporting medical activities and collaborating with cross-functional teams. I have a strong understanding of the responsibilities of an Associate Medical Manager, which include assisting in the development of medical strategies, supporting the dissemination of medical information, conducting literature reviews, and providing scientific expertise to internal and external stakeholders. I am familiar with medical compliance guidelines and regulations and have experience in managing medical programs and events.
- How do you stay updated with the latest medical and scientific advancements in your field?
Answer: Staying updated with the latest medical and scientific advancements is essential in the field of medical affairs. I regularly attend scientific conferences, symposiums, and webinars to stay abreast of the latest research and developments. I also subscribe to reputable medical journals and publications and participate in professional networks and associations. Additionally, I actively engage in continuous learning by pursuing relevant certifications and attending educational programs to enhance my knowledge and expertise.
- Can you provide an example of a successful medical project or initiative you have worked on and the impact it had?
Answer: In a recent project, I played a key role in the development and launch of a medical education program for healthcare professionals. I collaborated with internal teams and external experts to identify knowledge gaps and design an educational curriculum. I conducted literature reviews, developed educational materials, and organized live and virtual events. The program received positive feedback from healthcare professionals, and post-event evaluations showed improved knowledge and confidence in managing the specific medical condition. This initiative helped strengthen the company’s position as a trusted medical resource and enhanced our relationships with healthcare providers.
- How do you effectively communicate complex medical information to different stakeholders, including internal teams, healthcare professionals, and patients?
Answer: Effective communication of complex medical information is vital in the role of an Associate Medical Manager. I utilize clear and concise language to ensure understanding among different audiences. I adapt my communication style to the specific needs and knowledge level of the stakeholders. I leverage visual aids, such as slide decks or infographics, to enhance comprehension. I am also skilled at presenting scientific data in a meaningful and engaging manner, allowing stakeholders to grasp the key messages easily. Additionally, I actively listen to stakeholders’ concerns and provide timely and accurate responses to address their queries.
- How do you navigate and ensure compliance with medical regulations and guidelines in your work?
Answer: Navigating medical regulations and guidelines is a critical aspect of medical affairs. I have a thorough understanding of regulatory requirements and adhere to compliance guidelines in all my activities. I stay updated with changes in regulations and guidelines through regular training and collaboration with regulatory affairs teams. I maintain meticulous documentation and ensure proper record-keeping to demonstrate compliance. I also actively engage in cross-functional collaborations to ensure alignment with legal and regulatory requirements. By integrating compliance into my daily work, I ensure the highest standards of ethics and professionalism.
