Clinical Trial Liaison (EU)

CLINICAL TRIAL LIAISON

LOCATION:

Work will be performed remotely from home (from Germany) with significant travel to EMEA region study sites

SUMMARY:

Clinical Operations professional needed to provide clinical trial execution, compliance and site interface and communication support

DUTIES & RESPONSIBILITIES:

• Serve as sponsor contact for study sites and provide site training and education regarding study protocol, disease state, trial conduct, etc., and provide timely responses to related operational and technical questions
• Support pre-study feasibility assessment, study startup, enrollment, and compliance activities
• Grow and develop network of investigators and Key Opinion Leaders (KOLs)
• Team meetings and communications, reporting, and both remote and in-person study site visits
• Other duties, as required

QUALIFICATIONS & REQUIREMENTS:

• 6 years of relevant clinical operations experience including solid sponsor-side experience liaising with study sites and collaborating and driving trial enrollment, execution and compliance
• Solid experience with respiratory trials, including understanding of pulmonary testing, including FeNO and spirometry
• Experience as an MSL, Clinical Trial Educator, Clinical Trial Liaison, Nurse, Nurse Practitioner, Physician Assistant, and/or physician.
• Proven skills and experience building and managing relationships with investigators, other researchers, healthcare professionals, KOLs, and internal staff members across geographical borders
• Excellent written and verbal English (bi-lingual is a big plus) and interpersonal communication skills, and computer skills including Microsoft Office and standard clinical systems such as CTMS, EDC, eTMF and IRT)
• Relevant Bachelor's degree: Clinical, Healthcare or Scientific emphasis strongly preferred