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 clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.