Description

In this role, you will drive the strategy for cardiovascular projects while overseeing clinical research and ensuring compliance with regulations. Your responsibilities will include collaborating with health authorities, attending scientific events, and supporting medical publications.

Requirements

• •Strong teamwork skills and ability to work independently
• •Results orientation, initiative, flexibility, good organizational, prioritization, and time management skills
• •Strong communication, presentation, and interpersonal skills
• •MS Office skills, especially Word, Excel, and PowerPoint
• •Medical education and doctorate degree (MD, PhD)
• •Specialization in Cardiology
• •Work experience of more than 5 years in a clinical environment
• •Experience in drug development (clinical phases I-III)
• •Industry experience in Medical Affairs in the Cardiology space
• •Understanding of PET imaging and other imaging modalities

Tasks

• •Execute the overall strategy for LMI's cardiovascular pipeline
• •Oversee company-sponsored clinical research in cardiovascular indications
• •Provide input on study-related documents
• •Supervise medical and safety aspects of ongoing clinical trials
• •Support launch strategies and life-cycle management
• •Expand indications for use
• •Assist with medical publications
• •Liaise with health authorities for drug access
• •Maintain awareness of scientific, clinical, competitive, and regulatory developments
• •Attend scientific meetings and conferences
• •Develop summaries of key data and presentations
• •Implement quality assurance system guidelines
• •Ensure compliance with local and global laws and regulations

Tools & Technologies