Site Management Specialist
1 dzień temu
Real-World Evidence
Hybrid: EMEA
Unlock Your Potential
IQVIA Real-World Evidence (RWE) teams collaborate with clients to harness the power of real-world data and generate evidence to drive healthcare decision-making. Our innovative approach is redefining the industry, and we're seeking talented individuals to join our award-winning department.
Key Responsibilities
- Develop strong relationships with site personnel and stakeholders to ensure seamless project execution.
- Gain hands-on experience in study procedures, site selection, initiation, monitoring, and close-out visits.
- Evaluate site practices and quality, escalating any issues to Clinical Operations Lead and/or Line Manager.
- Manage study activities, tracking progress, and reporting to Line Management and Project teams.
- Collaborate with functional groups, such as Project Management, Regulatory Start-Up, and Epidemiology.
Requirements
- Bachelor's Degree in life science or healthcare, or equivalent combination of education and experience.
- Prior relevant experience is an asset.
- Awareness of clinical research regulatory requirements, such as GCP and ICH guidelines, is preferred.
- Excellent written and verbal communication skills, including proficiency in English and French.
- Computer skills, including Microsoft Office and IQVIA tools.
- Organizational, planning, interpersonal, and problem-solving skills.
What's in it for you?
- Global exposure and variety of therapeutic areas.
- Collaborative and supportive team environment.
- Access to cutting-edge technology and career development opportunities.
- Work-Life Balance and opportunities for growth.
Join IQVIA
- Embrace your curiosity and grow your career in a dynamic environment.
- Think boldly and disrupt conventional thinking.
- Enjoy what you do.
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