TFS HealthScience is a leading mid-sized Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Our Clinical Operations team, led by industry experts, combines the full-service capabilities and global reach of a large CRO with the flexibility and personal approach of a mid-sized CRO.
As a member of our SRS team, you will be dedicated to a single sponsor based in Greece. This is a contract-based position.
Responsibilities:
Relationship Building: Develop and maintain strong relationships with key personnel at clinical trial sites, including principal investigators, site coordinators, and other relevant staff.
Liaison Role: Act as a bridge between the company and clinical trial sites, ensuring clear and timely communication of study protocols, updates, and other essential information.
Issue Resolution: Address and resolve site-level issues, including challenges related to patient recruitment, protocol adherence, and data quality.
Training and Support: Provide training and support to site personnel, organize training sessions, and ensure that sites are well-informed about study procedures and updates.
Performance Monitoring: Monitor site performance, assess adherence to protocols, and identify and mitigate risks associated with site activities.
Collaboration: Work with cross-functional teams within the organization, including clinical operations, regulatory affairs, and data management.
Reporting: Track and report key performance metrics related to site activities, patient recruitment, and data quality.
Requirements:
Bachelor's degree in a relevant field (e.g., life sciences, nursing, healthcare management).
Proven experience in clinical research, focusing on site management or relationship management.
Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
Excellent communication and interpersonal skills.
Ability to problem-solve and address challenges proactively.
Experience in training and supporting site personnel.
Strong organizational and project management skills.
Willingness to travel for site visits as needed.
Contract Type:
0.8 FTE – 1.0 FTE
If you're passionate about making a meaningful impact in the field of clinical research and excited to be part of a global team committed to excellence, we look forward to receiving your application soon.
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