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Medical Liaison Specialist Leuven (BE) • Oxford Global Resources
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Leuven (BE)
Explore a unique opportunity as a Medical Liaison Specialist, where your scientific skills support a global Scientific Advisory Board with renowned Key Opinion Leaders. In this role, you will engage daily with experts, review study protocols, and prepare concise summaries. You will also recruit new board members and maintain the board's library. Enjoy a hybrid work model, with the flexibility of working from home three days a week. Join a dynamic team and expand your professional horizons. Discover why our team could be the perfect fit for you.
Over het bedrijf
Oxford Global Resources
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Are you a CRA interested in a new and slightly different challenge? Join a dynamic and impactful role as a Medical Liaison Specialist, where you'll leverage your scientific expertise to support the operations of a global Scientific Advisory Board composed of internationally recognized Key Opinion Leaders.
Job description
In this dynamic role of 'Medical Liaison Specialist', you can utilize your experience to expand your professional horizons and actively contribute to the growth and effective operation of the Scientific Advisory Board, which comprises Key Opinion Leaders from around the globe.
Responsibilities
- Engage in both oral and written communication on a daily basis with Key Opinion Leaders and members of the Scientific Advisory Board.
- Clarify the teams' expectations regarding study protocol reviews.
- Review study protocols across various indications, along with the consultancy reports prepared by the members of the Scientific Advisory Board. Subsequently, prepare concise summaries of these reports for the teams.
- Identify and recruit new members for the Scientific Advisory Board across various countries and therapeutic indications.
- Maintain the Scientific Advisory Board library by uploading reviews and ensuring the database is updated with new members.
- Coordinate and monitor payments, in cooperation with the Finance Department.
- Manage consultancy agreements, including tracking expiry dates and facilitating extensions as needed, in cooperation with the Legal Department.
Requirements
- University degree in Life Sciences or an equivalent combination of education, training & experience
- 2-3 years of experience as a Clinical Research Associate or in a similar role, specifically involving the understanding of study protocols across different indications.
- Experience in communicating with investigators is required, while experience in engaging with Key Opinion Leaders is a plus.
- Analytical mindset, advanced critical thinking skills along with good attention to detail
- Ability to work both independently and in a team environment
- Ability to plan, multitask and work in a dynamic team environment
- Experience working in an international team and effective communication in English
- Working proficiency in MS Word, Excel and PowerPoint
Additional information
- Full-time role
- Hybrid working : 2 days/week in the office + 3 days/week home-based.
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