Position Summary

CR-MSL is a field-based role with up to 80% time spent in field. CR-MSL will closely collaborates with RCO and global team to develop strategy and drive Phase 1-3 clinical trial activities as per plan.

Responsibility

1. Support Clinical Trial Activities

• Support Clinical Operations and Non Regulatory Data generation studies, including input on study feasibility, identification and assessment of potential study sites, facilitate investigator activities, and conduct site visits to support patient recruitment and/or discussions as needed.
• Provide recommendations and insights to GCO on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators.
• Actively support CRO sponsored studies as appropriate.
• Provide medical support to RCO to transition patients from clinical trial to marketed and/or reimbursed supply of drug, where required and appropriate.
• Ensure that pharmacovigilance procedural documents are understood and applied by Investigators of local studies, and alert appropriate personnel to any identified Adverse Events.

2. External Engagement and Insights

• Develop and maintain strong working relationships with key Thought Leaders in a disease area, gathering insights on current and future disease management and scientific perspectives including unmet clinical needs. Help understand insights gathered from scientific conversations to inform medical activities and clinical research locally and globally, as well as internal stakeholders where appropriate.
• Engage in scientific dialogue around current and emerging data through field visits, presentations and discussions and at scientific congresses. It is anticipated that a MSL will spend up to 80 percent of their time engaged with external customers with the balance of the time spent as a valued member of the medical team.
• Be a proactive member of Medical organization providing field medical insights and contributions.

Requirements

• 1+ years’ experience in a medical, scientific and/or clinical research environment
• Medical doctor (physician), PhD or PharmD, with experience with a broad medical or scientific background are preferred or Science graduate with substantial and relevant pharmaceutical experience

Required Competencies

• Discussing scientific or clinical data and collect medical insights from healthcare professionals
• Effectively listening, communicating and presenting scientific and/or clinical data to research or healthcare professionals
• Developing peer-to-peer relationships with top-ranking doctors, scientists or other healthcare professionals
• Training others
• Quickly and comprehensively learning about new subject areas and environments

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com