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

amplity; Deutschland; A distancia; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

Amplity is seeking an experienced Clinical Trial Liaison (CTL) to support clinical development programs across the DACH region. This field-based role serves as the local sponsor representative, driving site engagement, study start-up, patient recruitment, enrolment, and trial execution in a remote/field-based setting.

The CTL will collaborate with Clinical Operations, investigators, site personnel, CRO partners, and cross-functional teams to deliver studies to the highest quality standards,

Responsabilidades

• 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 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 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 elevate 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 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.
• Develop and maintain strong relationships with investigators, study coordinators, research nurses, and site personnel.
• Collabo

Descripción del empleo

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 elevate 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.

Collabo