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Medical Science Liaison

  • Location:

    Haarlem, Netherlands

  • Contact:

    Quinton Maduro

  • Job type:

    Contract

  • Contact phone:

    +31 (0)20 406 97 50

  • Industry:

    Pharmaceutical

  • Contact email:

    quinton_maduro@oxfordcorp.com

Our client, a prominent organization in the pharmaceutical industry, is looking for a medical science liaison. This is a fully remote position with substantial travel throughout Europe. The ideal candidate will have the expertise to drive clinical study recruitment efforts and accelerate progress for ongoing Phase II and III studies.
Job Description
In this role, you will be responsible for accelerating patient recruitment for Phase II and III clinical studies. Working closely with medical affairs, clinical development, and global clinical operations teams, you will develop and implement strategic plans to optimize study site engagement and enhance recruitment rates. By identifying and resolving site-specific barriers, you will play a pivotal role in ensuring the smooth execution of these studies. This position requires regular site visits and relationship-building with external experts, investigators, and study coordinators to advance study goals.
Responsibilities

  • Create and execute a weekly visit schedule to assigned study sites, focused on patient recruitment acceleration.
  • Develop strategic plans and clear communication frameworks to expedite study progress.
  • Collaborate transparently and share updates with clinical development and medical affairs teams.
  • Identify and address challenges at study sites, creating solutions in coordination with relevant teams.
  • Build and maintain relationships with investigators, site staff, and other key personnel involved in the studies.
  • Serve as a medical expert on products and disease areas to support and educate internal teams.
  • Ensure compliance with all company policies, ethical standards, and regulatory requirements in study execution.

Requirements

  • MD, PhD, or equivalent in life sciences.
  • At least 6 years of experience in clinical research within the pharmaceutical industry or a Contract Research Organization (CRO).
  • In-depth understanding of drug development processes, clinical trial management, and regulatory requirements for Phase II and III studies.
  • Proven experience working with external experts and study investigators.
  • Strong track record in clinical recruitment strategy and execution.
  • Ability to set direction, work effectively within matrix teams, and maintain excellent interpersonal skills.
  • Exceptional problem-solving skills with a results-driven approach.
  • Excellent written and verbal communication skills.
  • Strategic mindset, with a creative, solutions-oriented approach.
  • Adaptable to a fast-paced, dynamic environment with the ability to manage multiple clinical projects.
  • High ethical standards and integrity, with a commitment to transparency and collaboration in a global setting.

What We Offer

  • Contract: long term with prospect of permanent employment
  • Salary range: €5300,- to €6300,- depending on experience
  • Region: Fully remote role with significant travel across Europe.
  • Vacaturenummer: 25238