Clinical Trial Liaison (CTL) - Oncology, Hematology & Cardiovascular - Germany

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them.
Clinical Trial Liaison (CTL)
Oncology, Hematology & Cardiovascular Clinical Development
Business Unit: Clinical Operations – outsourced through Amplity
Reports to: Program Director, Amplity
Location: Germany preferred (Austria or Switzerland also considered)
Territory: DACH (Germany, Austria & Switzerland)
Role Type: Individual Contributor
Working Model: Field-Based / Remote
About the Role
Amplity is partnering with a leading global biotechnology company committed to transforming the treatment landscape through innovative clinical research across multiple therapeutic areas.
We are seeking an experienced Clinical Trial Liaison (CTL) to support clinical development programs across the DACH region. This field-based role will act as the local sponsor representative, supporting site engagement, study start-up, patient recruitment, enrolment, and overall clinical trial execution.
The successful candidate will work closely with Clinical Operations, investigators, site personnel, CRO partners, and cross-functional stakeholders to ensure studies are delivered efficiently while maintaining the highest standards of quality and compliance.
This position will support a portfolio of innovative clinical trials across multiple therapeutic areas, including Oncology, Haematology, and Cardiovascular/Metabolic Diseases, offering a unique opportunity to contribute to scientific advancement and improved patient outcomes.
Why Join This Opportunity?
Meaningful Scientific Impact
Support innovative clinical development programs in areas of significant unmet medical need.
Diverse Clinical Portfolio
Work across multiple therapeutic areas including oncology, haematology, and cardiovascular/metabolic diseases, gaining broad clinical development exposure.
Strategic Field-Based Role
Act as a key connection between investigator sites, sponsors, and clinical operations teams, helping drive study success throughout the trial lifecycle.
International Collaboration
Partner with investigators, healthcare professionals, and cross-functional teams across the DACH region and globally.
Professional Development
Join a highly collaborative environment that supports continuous learning, scientific excellence, and career growth.
Purpose of Role
The Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company across one or more countries within the DACH region.
The CTL interacts directly with investigator sites and clinical trial stakeholders, providing regional and country-specific insights to support study feasibility, site identification, site activation, patient recruitment, enrolment, and retention initiatives.
Working in close collaboration with Clinical Operations and Clinical Development teams, the CTL identifies operational challenges at investigator sites and helps facilitate solutions to support successful study delivery.
Key Responsibilities
Site Management & Clinical Trial Support
Provide country and regional operational insights to support site feasibility, site selection, and patient recruitment strategies.
Participate in Clinical Study Team meetings and operational review meetings, providing feedback and recommendations based on interactions with sites and investigators.
Attend and present at investigator meetings, monitor workshops, and other study-related activities.
Participate in site visits with investigators, study coordinators, site personnel, and CRO representatives to support clinical trial execution.
Support study start-up activities, enrolment initiatives, and issue resolution at investigator sites.
Review, document, track, and follow up on site-related issues and escalate where appropriate.
Act as the sponsor's regional operational support representative and point of escalation for investigator sites.
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 initiatives and operational excellence activities.
Perform triggered oversight monitoring activities as required and provide relevant reporting and feedback.
Ensure all activities comply with SOPs, GCP requirements, study protocols, and applicable regulations.
Act as a field-based source of scientific and clinical expertise for study sites.
Investigator Engagement & Relationship Management
Develop and maintain strong relationships with investigators, study coordinators, research nurses, and site personnel.
Collaborate with investigator sites to support patient recruitment and retention efforts.
Facilitate effective communication between study sites and internal stakeholders.
Support identification of barriers to enrolment and help implement practical solutions.
Engage appropriately with Key Opinion Leaders (KOLs) and healthcare professionals involved in clinical development programs.
Clinical Trial Recruitment & Enrollment
Support clinical trial recruitment strategies across assigned studies.
Identify opportunities to enhance site performance and patient enrolment.
Share best practices and operational insights across study teams.
Support the development of referral pathways and regional recruitment initiatives where appropriate.
Cross-Functional Collaboration
Collaborate closely with Clinical Operations, Clinical Development, Medical Affairs, Regulatory Affairs, and Clinical Project Management teams.
Gather and communicate actionable field insights to support study execution and strategic decision-making.
Provide regular updates on site activities, challenges, opportunities, and performance metrics.
Support broader clinical development initiatives and special projects as required.
Compliance & Quality
Operate in a highly ethical manner and comply with all applicable laws, regulations, GCP requirements, and company policies.
Maintain accurate and timely documentation of field activities.
Ensure all interactions with investigators and sites meet compliance standards.
Complete required training and certification activities within designated timelines.
Required Qualifications & Experience
Education
Pharmacist, PhD, MSc, or equivalent qualification in a relevant scientific discipline preferred.
Bachelor's degree in Life Sciences or related field minimum requirement.
Fluent written and spoken English required.
Fluent written and spoken German required.
Experience
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
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 working within Oncology, Haematology, Cardiovascular, or Metabolic clinical trials is highly desirable.
Experience engaging investigators, study coordinators, and healthcare professionals across multiple sites and countries preferred.
Skills
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 while contributing effectively 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.
Travel Requirements
Approximately 50–60% travel within the DACH region.
Overnight travel required as needed.
International travel may be required.
Valid driver's license required.
What We Offer
Meaningful Impact
Support innovative clinical development programs with the potential to impro