Medical Scientific Liaison – PJ (Ref ID: 11573)
・To support Medical Affairs Manager on aspects of Scientific and Medical Affairs.
・Train the medical, marketing and sales teams on the disease background and pharmaceutical and clinical data of the products.
・Provide scientific & medical support on product promotion activities, including material development such as Guidelines, Pamphlets, Brochures, Q&A and etc., advertising messages, CMEs and relationship building activities, directed to healthcare professionals, patients and lay public and ensure that all of these comply with legal, local regulatory, industry and corporate guidelines & Code of Ethics.
・Monitor and challenged unfounded and misleading promotional claims and unethical programs by competitors to ensure fair marketing promotions.
・Provide scientific information and documents required by health authorities in order to facilitate approval of product registration.
・Provide response to queries or complaints from health authorities, healthcare professionals and the lay public on the company products.
・Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development
・Support the medical community with up-to-date medical information, robust disease expertise, and product information
・Degree in chemistry, biology, pharmacy, or other medical related discipline
・ Minimum 6 months experience in Pharmacovigilance experience
・An extensive medical (including training) and scientific background as well as client education experience in the pharmaceutical industry specifically on the field of Dermatology and Respiratory and Paediatrics
・Clear knowledge of international and local pharmaceutical guidelines and government laws.
・Proven ability to communicate clearly with physicians and health-care professionals regarding medical products, procedures and research data.
・Support clinical development initiatives including site identification, trial recruitment, registry, and final approved data