Medical Science Liaison
Derks&Derks
A temporary position for the period of 6 months at a global pharmaceutical company
Offer
- a challenging job within a global pharmaceutical company
- an operational role in an international environment
- a temporary contract till 01-07-2025
Position
As Medical Science Liaison you are responsible for driving patient recruitment for Phase II & III clinical studies. In this role, you will be responsible for developing and executing strategies to accelerate patient recruitment across study sites. You will maintain a consistent presence through weekly face-to-face visits with site staff to monitor progress and proactively address any challenges that may impede study timelines.
Key responsibilities include crafting strategic and communication plans to support recruitment acceleration and collaborating closely with Medical Affairs, Clinical Development, and Global Clinical Operations (GCO) teams. You will identify and resolve site-specific barriers, working to ensure seamless study execution and adherence to all ethical and regulatory standards. As a Medical Science Liaison, you will also build and maintain strong professional relationships with external experts, investigators, and site coordinators. Additionally, you will serve as an internal expert on disease and product-related information, educating teams to enhance study execution. This role requires a commitment to compliance and excellence in advancing our clinical studies and patient impact.
In short, as a Medical Science Liaison, you will drive patient recruitment for Phase II & III studies, develop strategies to accelerate recruitment, conduct regular site visits, and resolve study challenges. You will collaborate closely with teams, build relationships with external experts, and serve as an internal expert, ensuring compliance and supporting effective study execution.
Profile
- MD/PHD or other life sciences degree required;
- minimum of 6 years of pharmaceutical industry/CRO clinical research experience;
- broad knowledge of drug development, clinical trial execution, regulatory requirements for phase II & III studies;
- skilled in developing and implementing strategies for accelerated patient recruitment;
- strong track record of successful patient recruitment in Phase II & III clinical studies;
- ability to lead and align cross-functional, matrixed teams with exceptional interpersonal skills;
- excellent Polish communication skills, both verbal and written.
Organisation
Our client is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Their employees are at the core of their success, with colleagues in over 80 countries, delivering the world’s largest medicine cabinet to 200 million people every day. They offer a unique, diverse portfolio of products and solutions for patients and they have built a promising pipeline centered around their core therapeutic areas. They are continually developing patient-centric solutions and significantly growing both their generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how they improve health and enable people to live better, healthier lives.
Response
Interested? Please send your resume by e-mail, with reference to MSP/24-355, to Annerien Peters: info@derksenderks.nl. For further information, please call Annerien at number +31 (0)6 45403933.
Our client has chosen Derks & Derks Secondment & Interim as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.
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