Description

In this role, you will manage medical information processes, ensuring timely and compliant responses to inquiries while collaborating with experts. You will also contribute to educational activities and maintain databases to support various teams.

Requirements

• •PhD or Master’s degree in Life Sciences or equivalent
• •At least three years of experience within the Pharmaceutical Industry
• •Ability to evaluate and analyze medical/scientific literature
• •Presentation skills
• •Experience in Medical Writing
• •Excellent written and verbal communication skills in English
• •Experience with Literature databases (Embase, Medline)
• •Experience in MS Office, specifically MS Excel
• •Knowledge of Tableau or similar analysis software
• •Collaborative team player with interpersonal skills
• •Sense of accountability and ownership
• •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
• •Ability to work independently
• •Ability to engage with key external stakeholders
• •Prioritization and time management skills

Tasks

• •Oversee processes and agreements related to medical information at HQ and affiliates
• •Stay informed about available medical information systems
• •Manage general MedInfo tasks and inquiries
• •Attend Medical Affairs/Information booth at scientific congresses as needed
• •Ensure compliance with copyright regulations for scientific literature provision
• •Follow medical information processes for timely, high-quality responses
• •Identify, escalate, and record adverse events and product quality complaints
• •Build and maintain in-depth knowledge of Sobi’s product portfolio
• •Collaborate with subject matter experts to handle incoming medical inquiries
• •Maintain documentation and tracking of inquiries and responses
• •Identify frequent medical information inquiry topics
• •Develop and maintain standard response letters (SRLs) and FAQs
• •Support the creation of non-standard responses
• •Provide reports and listings to partners and internally
• •Contribute to medical educational activities and non-promotional material development
• •Stay updated on scientific information in assigned areas
• •Build and maintain cross-functional relationships
• •Conduct literature analyses
• •Create and maintain product-specific literature databases
• •Perform metrics analyses of published articles to support cross-functional teams

Tools & Technologies