Clinical Trial Liaison – Oncology, Hematology, Cardiovascular

🔥 12 hours ago

🌐 Germany, Austria, +1 more countries – Remote

🇩🇪 Germany – Remote 🇦🇹 Austria – Remote 🇨🇭 Switzerland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Liaison

👻 Ghost score 10%

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Amplity Health

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

Amplity Health is a global contract sales and commercial organization partnering with pharmaceutical and biotechnology companies to provide tailored outsourced programs and communications throughout a drug's life cycle. They specialize in scientific stakeholder engagement and go-to-market strategies by emphasizing person-to-person interactions with physicians, patients, payers, community organizations, and life science executives. Amplity manages and employs stakeholder-facing professionals globally to ensure that more patients gain access to the best medicines. Their expertise includes oncology, rare diseases, and specialty therapies, with a focus on precision medicine solutions. Amplity's services extend to medical communications, market access, commercial sales, and providing real-time insights through proprietary AI-powered technology to enhance stakeholder engagement.

📋 Description

• Support clinical development programs across the DACH region as the local sponsor representative • Support site engagement, study start-up, patient recruitment, enrolment, retention, and overall clinical trial execution • Work with Clinical Operations, investigators, site personnel, CRO partners, and cross-functional stakeholders • Provide country and regional insights for site feasibility, site selection, and patient recruitment strategies • Participate in Clinical Study Team and operational review meetings • Attend and present at investigator meetings, monitor workshops, and study-related activities • Participate in site visits with investigators, study coordinators, site personnel, and CRO representatives • Review, document, track, follow up, and escalate site-related issues • Act as the sponsor's regional operational support representative and escalation point • Support investigator site readiness and study performance throughout the trial lifecycle • Participate in regulatory inspections and audits as a sponsor representative when required • Contribute to process improvement and operational excellence initiatives • Perform triggered oversight monitoring activities and provide reporting and feedback • Ensure compliance with SOPs, GCP requirements, study protocols, and applicable regulations • Provide scientific and clinical expertise to study sites • Develop and maintain relationships with investigators, study coordinators, research nurses, and site personnel • Support patient recruitment and retention efforts and identify enrolment barriers • Engage with Key Opinion Leaders and healthcare professionals • Share best practices and operational insights across study teams • Support referral pathways and regional recruitment initiatives • Collaborate with Clinical Operations, Clinical Development, Medical Affairs, Regulatory Affairs, and Clinical Project Management teams • Communicate field insights, site updates, challenges, opportunities, and performance metrics • Support broader clinical development initiatives and special projects

🎯 Requirements

• Candidates must be based in Germany, Austria, or Switzerland • Bachelor's degree in Life Sciences or related field minimum requirement • Pharmacist, PhD, MSc, or equivalent qualification in a relevant scientific discipline preferred • Fluent written and spoken English required • Fluent written and spoken German required • Minimum 5 years of relevant pharmaceutical, biotechnology, CRO, or clinical research experience • Strong clinical trial site management experience required • Previous experience as a Clinical Research Associate (CRA), Senior CRA, Clinical Trial Liaison (CTL), Clinical Operations Specialist, Clinical Study Manager, or Medical Science Liaison with significant clinical trial responsibilities • Strong understanding of clinical trial methodology, site management, and clinical development • Experience supporting patient recruitment, enrolment, and study execution activities • Experience within Oncology, Haematology, Cardiovascular, or Metabolic clinical trials highly desirable • Experience engaging investigators, study coordinators, and healthcare professionals across multiple sites and countries preferred • Excellent communication and stakeholder management skills • Strong interpersonal and relationship-building abilities • Ability to communicate scientific and technical information clearly and effectively • Strong organizational and prioritization skills • Ability to work autonomously within a cross-functional team environment • High ethical standards and sound scientific judgment • Strong understanding of ICH-GCP requirements • Demonstrated ability to work successfully within international clinical research environments • Approximately 50–60% travel within the DACH region • Overnight travel required as needed • International travel may be required • Valid driver's license required • CV must be submitted in English

🏖️ Benefits

• Field-based role with a high level of independence and ownership • Ongoing training and development opportunities • Exposure to global clinical development programs • Collaborative environment with experienced clinical development professionals, investigators, and healthcare experts • Competitive compensation package • Comprehensive benefits • Long-term career development opportunities