Global Medical Information and Knowledge Management (9 Months contract)

Key responsability

• Keep overview over processes and agreements involving medical information at HQ affiliates as well as service providers contracted
• Stay informed about Medical Information related systems available General MedInfo tasks and -inquiry management
• Presence at Medical Affairs/Information booth at scientific congresses if needed
• Ensure that provision of scientific literature to internal and external customers is compliant with copyright regulations
• Follow current medical information processes for the creation and timely provision of high quality medical information responses to internal and external customers
• Identify escalate and record adverse events and product quality complaint associated with medical information inquiries
• Build and maintain deep knowledge and understanding about Sobis product portfolio
• Responsible for the collection and handling of incoming medical inquiries in collaboration with subject matter experts in adherence to all applicable rules regulations and SOPs
• Maintain appropriate documentation/tracking of inquiries and responses
• Responsible for the identification of areas that are the subject of frequent medical information inquiries
• Responsible for the development and maintenance of standard response letters (SRLs) and frequently asked question (FAQs) documents as well as for the creation of Non Standard Responses
• Support the development and maintenance of SRLs and FAQs
• Provision of reports and listings to partners and internally
• Contribute to medical educational activities (eg training material literature updates journal clubs) and development of non-promotional material in collaboration with the Medical & Scientific Affairs team if needed
• Keep abreast of scientific information and knowledge in assigned areas Builds and maintains cross-functional relationships Literature analyses
• Create product-specific literature databases maintain these databases and create metrics analyses of articles published to support the work of several cross-functional teams within Medical Affairs and beyond.

Qualifications :

Desired Experiences/Competencies

• PhD or Masters degree in Life Sciences or equivalent
• Experience of at least three years within the Pharmaceutical Industry
• Demonstrated ability to accurately and effectively evaluate and analyze medical/scientific literature
• Presentation skills
• Experience in Medical Writing
• Excellent written and verbal communication skills in English
• Experienced in working with Literature databases (Embase Medline)
• Experienced in MS Office specifically MS Excel
• Knowledge on Tableau or similar analysis software Personal attributes
• Collaborative team player with interpersonal skills able to work effectively in a team setting and interact respectfully with people of different cultural seniority and functional backgrounds
• Sense of accountability and ownershi
• Results oriented Entrepreneurial driven and engaged
• High scientific and ethical integrity
• Flexible and able to operate in a quickly changing environment
• Strong attention to detail and diligence
• Able to work independently
• Ability to engage with key external stakeholders
• Prioritization and time management skill

Remote Work :

Yes

Employment Type :

Full-time