Clinical Trial Liaison, Oncology

The Medical Affairs Company (TMAC); Österreich; Vor Ort; EUR 80.000 - 110.000; Vollzeit

Zusammenfassung

The Clinical Trial Liaison (CTL) at The Medical Affairs Company (TMAC) will serve as the local field-based representative for global development programs. You will provide regional insights for site feasibility, recruitment strategies, and investigator engagement.

With 8+ years in clinical trial operations, you will support study teams in feasibility, startup, enrolment, and issue escalation while ensuring adherence to ICH/GCP and regulatory requirements, and you will travel frequently within

Qualifikationen

• Bachelor's degree required.
• 8+ years of industry and/or CRO experience.
• Oncology clinical trial experience preferred.
• Fluency in English and local language.
• Working knowledge of ICH/GCP.
• Strong communication and interpersonal abilities.
• Proficient in Excel, Word, and PowerPoint.

Aufgaben

• Provide country/regional operational insight into site feasibility and recruitment strategy.
• Participate in Clinical Study Team Meetings and Quality Review Meetings with input on operational issues.
• Attend investigator meetings and monitor workshops/training.
• Support site visits with investigator staff or CROs; report on feasibility, startup, enrolment or site issues.
• Review, document, and follow up on investigator site issues with metrics tracking.
• Provide sponsor regional operational support and act as escalation point for sites.
• Participate in Regulatory GCP inspections or audits at investigator sites.
• Complete administrative tasks per SOPs including field activity documentation and expense reporting.
• Manage travel and local expenses per sponsor and TMAC policies.

Kenntnisse

Clinical trial operations

Site liaison

Regulatory knowledge

Communication skills

Interpersonal skills

Project coordination

Ausbildung

Bachelor's degree

Master's degree preferred

MD/PhD/PharmD

Tools

Excel

Word

PowerPoint

Jobbeschreibung

The Clinical Trial Liaison (CTL) supports Global Development clinical study execution as the local field-based representative for the sponsor company in one or more countries/regions supporting clinical development programs. The CTL interacts with investigator sites and other parties related to clinical trial execution.

The CTL provides regional and country specific insights to support study feasibility, site identification and selection, and patient recruitment and retention initiatives. In collaboration with the study team, the CTL both identifies and helps facilitate resolution of investigator site issues.

Duties and Responsibilities:

• Provide country/regional operational insight into site feasibility and selection and overall patient recruitment strategy
• Participate in Clinical Study Team Meetings and Quality Review Meetings where necessary providing input to study teams on operational issues based on site visits and contacts
• Attend and present at investigator meetings, monitor workshops/training
• Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e.g. feasibility, startup activities, enrolment or escalated study/site issues
• Responsible for review, documentation and follow up of investigator site issues including tracking metrics
• Provides sponsor regional operational support and acts as point of escalation for investigator sites as appropriate
• Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative
• Complete all administrative responsibilities consistent with SOPs and departmental guidelines including but not limited to required training, field activity documentation, expense reporting, and other assigned tasks
• Manage travel and local expenses in accordance with sponsor and TMAC policies

Qualifications and Experience:

• Minimum Bachelor's degree, master's preferred or terminal degree (MD, PhD or PharmD)
• 8+ years relevant industry and/or CRO experience required
• Extensive experience in global clinical trial operations required
• Oncology clinical trial experience preferred
• Extensive medical and scientific knowledge and clinical development understanding
• Excellent communicator of technical and scientific information
• Excellent interpersonal skills and demonstrated collaborative as well as independent working style
• Ability to build relations with the external medical community
• Proactive and self-motivated, ability to align activities with the clinical development plans (CDPs)
• Strong organizational skills with effective use of time and prioritization
• Fluency in English and in local language in country of residence required
• A working knowledge of ICH/GCP
• Computer skills including Excel, Word, and PowerPoint
• A willingness to travel frequently within assigned geographical territory, including overnight travel.