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    Medical Information Specialist - Île-de-France - Indegene

    Indegene
    Indegene Île-de-France

    il y a 5 jours

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    Description

    Who we are?

    We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out

    What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it?

    We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers.

    We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you.

    If this excites you, then apply below.

    Summary: Indegene is looking for a France based medical information professional to work on medical information deliverables for their global clients. Key responsibilities would include literature searches, creating/updating standard response documents, and responding to medical information requests and escalated inquiries based on highest quality clinical evidence.

    Requirements:

    • Proficient with English, French and German/Italian/Spanish
    • Doctorate in research or pharmacy qualification (PharmD., Ph.D.)
    • 2-4 years of any type of scientific writing/content writing/publications, or research/grant writing experience in life sciences domain. Pharmaceutical industry (medical information, medical communication, medical affairs, safety, regulatory) experience would be preferable. Freshers with lab work/ research/PharmD background can be considered for this role.
    • Strong accountability, interpersonal and organizational skills, and the ability to work in a cross-functional team environment.
    • Ability to perform literature research, analysis and interpretation of medical data.
    • Excellent verbal and written communication skills and willingness to travel on as needed basis.

    Responsibilities:

    • Respond to medical information requests (or inquiries) from internal and external customers and ensure the responses are medically and scientifically accurate, timely, balanced, and meet customers' needs.
    • Respond to inquiries received via phone, email, internet or mail with high quality customer service and document the inquiry and response accurately and completely according to relevant Standard Operating Procedure (SOP) and regulatory guidelines.
    • Create medical information documents- standard response documents (SRs) by assessing and summarizing published medical and scientific literature. Update the documents at regular intervals and maintain a database of frequently used medical information documents.
    • Reporting issues of Adverse events and/or Product Quality complaint associated with the medical information as per the defined procedures and adhere to the required timelines.
    • Demonstrate expertise and knowledge of assigned therapeutic areas and a good understanding of pertinent disease state(s).
    • Deliver high quality literature search, including identification of key literature that would support the creation of medical content and check for or obtain copyright permissions prior to internal or external use.
    • Work on platforms and tools to support creation, review, management, documentation, analysis and tracking of medical information documents.
    • Work with the medical information and medical affairs teams during congresses, product launches, and key data releases and ensure assigned work is completed as per the timelines and SOPs.
    • Be a part of the training process and preparing specific training documents on need basis and imparting training as and when required.
    • Follow-up on safety/PQC information as requested by Drug Safety team

    NOTE: Please upload CV in English.

    EQUAL OPPORTUNITY

    Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate's merit and qualification.

    We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

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