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Senior Clinical Trial Liaison

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in a relevant field, Experience in clinical research, Strong understanding of GCP and regulations, Excellent communication and interpersonal skills, Proven problem-solving abilities.

Key responsabilities:

  • Develop relationships with clinical trial sites
  • Act as liaison for study communication
  • Resolve site-level issues and challenges
  • Provide training and support to personnel
  • Monitor site performance and report metrics
TFS HealthScience logo
TFS HealthScience Pharmaceuticals SME https://tfscro.com/
501 - 1000 Employees
See more TFS HealthScience offers

Job description

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

What Can We Offer You:

  • A Rewarding Career: Elevate your career in a global environment filled with growth opportunities.
  • Diverse and Dynamic Team: Join passionate experts from around the world who prioritize patients, saving lives, and improving their quality of life.
  • Competitive Compensation: Recognize your skills and dedication with a competitive salary.
  • Health and Well-being: Enjoy comprehensive preventative private healthcare solutions for you and your loved ones.
  • Career Advancement: Explore numerous career progression opportunities within our organization.
  • Supportive Leadership: Work with an excellent, highly experienced local manager who will guide and mentor you.
  • Positive Team Culture: Be part of a team that values a healthy work-life balance and fosters a supportive and positive work environment.

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.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Organizational Skills
  • Training And Development
  • Problem Solving
  • Collaboration
  • Social Skills
  • Problem Reporting
  • Relationship Building
  • Verbal Communication Skills

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