- Lorent y Cuencamedical writer and reviwerDecember 2020 - Today (4 years and 2 months)São Paulo, BrazilScientific Writing: Authored, updated, and refined a diversity of high-quality, scientifically accurate documents. This included clinical study reports, medical information brochures, medical education materials, promotional and non-promotional materials. These documents were designed to adeptly represent the scientific research, not only maintaining factual precision but also effectively conveying the potent implications of our work.Research: Executed comprehensive literature reviews and perpetually stayed up-to-date with new developments in correlated therapeutic areas. This thorough research has been pivotal in informing my writings, giving me the tools to generate nuanced, informed documents that contribute constructively to the existing body of knowledge.Collaboration: Collaborated intensively with the clinical research teams, assimilating profound understandings of the study design, goals, and outcomes. This intimate cooperation allowed me to accurately portray the projects' visions and accomplishments, reflecting the transformative work achieved by the teams.Quality Control: Scrutinized and proofread all documents, ensuring medical accuracy and strict compliance with regulatory guidelines. By consistently upholding high-quality standardsPromotional and Non-promotional Materials: Produced both promotional and non-promotional materials tailored to the needs of various stakeholders. All materials were created adhering to our stringent ethical principles, ensuring the accurate dissemination of information, fostering informed decision-making, and increasing the visibility of our research.Project Management: Managed and tracked the developmental timelines of a broad range of documents, coordinating efforts proficiently with both internal and external stakeholders. By maintaining a tight rein on the projects' lifecycle, I successfully ensured on-time completion of all documents upholding work productivity and efficiency, thus avoiding any project delays.
- CLS ViforScientific ManagerJuly 2022 - August 2023 (1 year and 1 month)• Functioned as a pivotal medical resource, offering extensive support to local operations and ensuring secure patient access to CSL Vifor products across the designated geographic region.• Orchestrated compelling clinical and scientific presentations aimed at internal and external audiences, effectively educating healthcare providers about disease state concepts.• Spearheaded internal training initiatives, rigorously adhering to global and local compliance regulations.• Authored comprehensive dossiers, reports, and supporting materials, while also assuming a critical role in reviewing content for publication and creating informative slide decks for scientific presentations.• Prepared assigned documents meticulously in accordance with CSL Vifor Standard Operating Procedures (SOPs) and customer requirements, consistently adhering to agreed timelines.• Played an integral role in clinical trials by providing extensive support to identify potential enrollment barriers, resolving issues within clinical sites, and actively participating in investigator meetings.• Collaborated seamlessly with cross-functional teams, including R&D, Medical Affairs, and Clinical Operations, fostering effective communication and streamlined trial operations.• Leveraged a profound understanding of common statistical methods employed in clinical trials, ensuring the ability to interpret and analyze their results effectively• Established and nurtured enduring, collaborative relationships with healthcare professionals (including physicians, nurses, and allied health professionals) within the allocated territory.• Represented the company and the Medical Affairs division during interactions with the medical and scientific community, contributing to the establishment of robust partnerships.
- Grunenthal GroupMedical Science LiaisonSeptember 2021 - July 2022 (10 months)• The role was setting of bringing the outside of the company, working with partners to uncover all potential opportunities to transform outcomes for patients• Bringing expertise, science and knowledge to the ecosystem• Acting as trusted partner, point of contact between stakeholders.• Sharing of the stakeholder and their patient's community needs, prioritize and secures resources, and drives solutions that delivering outcomes.• Building partnerships with stakeholders and institution to remove roadblocks and unlock possibilities to deliver value for patients and the community.• Stewards Roche's products through their lifecycle and supports their appropriate use, which includes sharing their merits with HCPs in a truthful and balanced manner.
Karina Morais recommend Jalile
- PhDUnicamp2019PhD in Molecular biology focus in Neuroscience MSc in Nutrition Science and Sports Pt