Medical Science Liaison

ESSENTIAL DUTIES & RESPONSIBILITIES Medical Communication & Education: Maximise your chances of a successful application to this job by ensuring your CV and skills are a good match. * Provide medical information to physicians, treatment center personnel, and patients regarding Kaneka Medical America products. * Lead content development for medical communications and education. * Conduct orientation sessions for clinical, marketing, and sales teams on clinical practices, research projects, guidelines, and adverse event handling. Collaboration & Relationship Management: * Regularly interact with sales, marketing, and clinical teams to address scientific inquiries. * Establish and maintain relationships with key customers, opinion leaders, treatment centers, and patient groups. * Engage with physicians and medical personnel at existing and potential LIPOSORBER customer sites. Clinical Study Support: * Support all new and ongoing clinical studies and related activities. * Assist in daily tasks related to clinical development projects and clinical study protocols. Scientific Insights & Presentations: * Present scientific information at professional meetings as needed. * Gather insights from key opinion leaders to conduct gap analyses and support strategic planning. Emotional Intelligence Skills: * Demonstrate empathy, adaptability, excellent communication, and interpersonal skills. OTHER RESPONSIBILITIES Maintain complete and open lines of communication with other personnel, functions, or departments to facilitate operations and interaction in the organization. Keep manager informed of status and progress, ensuring that regular and periodic communication takes place. Maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks and keeping abreast of industry trends and related compliance issues within the area of responsibilities. Maintain professional conduct, attendance, and high ethical standards in the workplace, complying with the company's policies and procedures. Fulfill mandatory training requirements applicable for department and job duties as appropriate. Perform other duties and responsibilities as required or requested by supervisor or Management. Assist with overseeing external vendors working on the study. Assist with site medical monitoring, data management, IRB application and interaction, pharmacovigilance, and other critical activities for FSGS post-approval study. Assist with clinical study protocol and protocol amendments. Prepare clinical documents, e.g., protocols, annual report updates, case report forms and clinical study reports, monitoring plans, and budget as requested by supervisor or Management. Assist management with new sites joining the adult and pediatric FSGS post-approval study. Support functional area management with medical content creation and review for targeted therapeutic areas. Qualifications Behaviors: Enthusiastic - Shows intense and eager enjoyment and interest Team Player - Works well as a member of a group Loyal - Shows firm and constant support to a cause Dedicated - Devoted to a task or purpose with loyalty or integrity Detail Oriented - Capable of carrying out a given task with all details necessary to get the task done well Education: Doctorate (required) PHD of Pre-Medicine (required) Bachelors of Pre-Medicine (required) Experience: 2 years: Therapeutic area experience: Cardiology & Nephrology (preferred) 1 year: Managing clinical studies (required) 1 year: Medical device/Pharmaceutical industry (required) 2 years: Scientific/Medical affairs (required) Skills: MS PowerPoint (required) MS Word (required) MS Outlook (required) MS Excel (required) Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities The contractor will not discharge or in any other manner discriminate against employees or applicants because they #J-18808-Ljbffr

Created: 2025-01-03