Clinical Trial Liaison Manager

Location: Basel
Contract: 12-month contract
Start Date: ASAP
Workload: Full-time

Overview:
Our client, a global pharmaceutical company, is looking for a Clinical Trial Liaison Manager (CTLM). This role is focused on trial delivery and oversight, ensuring high-quality data and timely patient recruitment.

Key Responsibilities:

• Acting as the sponsor’s main point of contact for site staff and investigators
• Supporting Principal Investigators in developing and executing enrolment strategies
• Collaborating with CRAs and site coordinators to improve recruitment and site performance
• Overseeing and tracking patient recruitment across assigned sites and countries
• Conducting Sponsor Oversight Monitoring Visits (SOVs) to ensure CRO monitoring quality
• Supporting site teams in maintaining protocol adherence and resolving operational issues
• Monitoring data quality through remote and on-site review
• Maintaining strong relationships with key sites and providing operational insights
• Escalating risks and challenges to internal trial teams or the CRO in a timely manner
• Ensuring compliance with GCP, local regulations, SOPs, and internal policies

Required Qualifications:

• Bachelor’s degree in pharmaceutical sciences, biology, healthcare, or related field
• Experience working with CROs and managing trial site performance
• Strong knowledge of the clinical trial landscape, including patient pathways and recruitment dynamics
• Skilled in stakeholder communication (internal teams, sites, KOLs, networks, CROs, etc.)
• Demonstrated leadership with the ability to influence without authority
• Proactive problem-solver with strong analytical and organizational skills
  Fluent in English and French (written and spoken) – additional languages are a plus
• Familiar with tools and systems used to manage clinical studies
• Willing to travel up to 60%

Please apply directly online with your CV.

**Please only apply if you are eligible to work in Switzerland and the EU*
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