Auf einen Blick
- Aufgaben: Unterstütze klinische Studien in der EMEA-Region und baue Beziehungen zu Forschungsteams auf.
- Unternehmen: Innovatives Unternehmen im Gesundheitswesen mit einem dynamischen Team.
- Vorteile: Flexibles Arbeiten von zu Hause, Reisegelegenheiten und Weiterbildungsmöglichkeiten.
- Weitere Informationen: Möglichkeit zur Verlängerung des Auftrags und hervorragende Karrierechancen.
- Warum dieser Job: Gestalte die Zukunft der Medizin und arbeite an spannenden klinischen Studien.
- Qualifikationen: Mindestens 6 Jahre Erfahrung in klinischen Studien und starke Kommunikationsfähigkeiten.
Das prognostizierte Gehalt liegt zwischen 63000 - 77000 € pro Jahr.
For our client, we are currently looking for an experienced Freelance Clinical Trial Liaison (CTL) to support clinical trial activities across the EMEA region.
The position is home-based in Germany , ideally in the Frankfurt area , with up to 60% travel to clinical study sites across EMEA .
The initial assignment is planned for 12 months, with the possibility of extension .
Responsibilities Serve as a key sponsor contact for clinical study sites across the EMEA region.
Provide training and education to study sites regarding study protocols, disease state, trial conduct and related requirements.
Respond to operational, scientific and technical questions from study sites and site personnel.
Support pre-study feasibility assessments.
Support study start-up activities.
Support patient enrollment and recruitment activities.
Support clinical trial execution and compliance activities.
Work closely with study sites to help drive successful trial enrollment and execution.
Develop and maintain relationships with investigators, researchers, healthcare professionals and Key Opinion Leaders (KOLs).
Build and expand networks of investigators and KOLs across the region.
Conduct remote and in-person visits to clinical study sites throughout EMEA.
Participate in study team meetings and regular project communications.
Provide reporting and documentation related to study and site activities.
Collaborate with internal and external stakeholders across different geographical regions.
Provide additional clinical operations support as required.
Requirements At least 6 years of relevant Clinical Operations experience .
Solid sponsor-side clinical trial experience .
Demonstrated experience liaising directly with clinical study sites.
Experience supporting and driving clinical trial enrollment, execution and compliance.
Strong experience with respiratory clinical trials .
Good understanding of pulmonary testing within a clinical trial environment, particularly spirometry and Fe NO .
Previous experience as a Medical Science Liaison (MSL), Clinical Trial Educator, Clinical Trial Liaison, Nurse, Nurse Practitioner, Physician Assistant and/or Physician is highly preferred.
Ability to understand study protocols and discuss scientific, medical and technical aspects of clinical trials with study personnel.
Proven experience developing and managing relationships with investigators, researchers, healthcare professionals and KOLs.
Experience working with stakeholders across geographical borders.
Excellent interpersonal and communication skills.
Excellent written and verbal English and German language skills.
Fluency in an additional EMEA-region language would be an advantage.
Experience with standard clinical systems such as CTMS, EDC, e TMF and IRT .
Strong Microsoft Office skills.
Relevant Bachelor's degree, preferably with a clinical, healthcare or scientific focus .
Freelance Clinical Trial Liaison (M/F/D) – EMEA | Germany Arbeitgeber: NES Fircroft
Unser Unternehmen bietet eine dynamische und innovative Arbeitsumgebung, in der Prozessingenieure für die Laserfertigung an vorderster Front der Technologie arbeiten. Wir fördern eine offene Unternehmenskultur, die Teamarbeit und kontinuierliches Lernen unterstützt, und bieten zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung. Zudem profitieren unsere Mitarbeiter von flexiblen Arbeitszeiten und einem attraktiven Standort, der eine hervorragende Work-Life-Balance ermöglicht.
