b Overview /b p In this fixed-term Medical Information Specialist role, you will deliver expert medical information to healthcare professionals, internal teams, and external stakeholders, ensuring accuracy and regulatory compliance. You will collaborate with medical affairs and regulatory groups to support content development and maintain audit-ready records. The position combines scientific support with process improvement in a dynamic life sciences environment. You will contribute to advancing patient care by delivering reliable, data-driven medical information and collaborating across functions. /p b Responsibilities /b ul li Deliver accurate, balanced, and timely medical information to healthcare professionals and internal teams. /li li Review and maintain medical content for regulatory compliance. /li li Partner with medical and regulatory teams to develop medical communication materials. /li li Analyse requests to craft appropriate scientific responses and escalate complex issues when needed. /li li Maintain detailed records of interactions and documentation to support compliance and audit readiness. /li li Improve processes and tools to enhance quality and efficiency of medical information delivery. /li /ul b Key requirements /b ul li Experience in medical information, pharmacovigilance, or medical affairs in the life sciences sector. /li li Strong knowledge of medical terminology, regulatory standards, and medical writing. /li li Excellent communication skills and ability to liaise with diverse stakeholders. /li li Familiarity with medical content management systems and scientific databases. /li li A relevant degree in life sciences, pharmacy, or related discipline. /li li Eligibility to work on a fixed-term contract in the UK. /li /ul ul li Excellent communication skills /li li Stakeholder liaison /li li Attention to detail /li li Medical content management systems /li li Scientific databases /li li Medical writing /li /ul
Medical Information Specialist FTC - UK employer: Meet Life Sciences
Join a dynamic and innovative pharmaceutical organisation in Egham, Surrey, where you will be part of a collaborative team dedicated to advancing clinical research. We offer a hybrid working model that promotes work-life balance, alongside opportunities for professional development and growth within the clinical operations field. Our supportive culture values your contributions and encourages continuous improvement, making it an ideal environment for those seeking meaningful and rewarding employment.