ICON Clinical Research
7 months ago
Senior CRA
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Company information
- Company
- ICON Clinical Research
- Location
- New Zealand New Zealand
- Posted
- 7 months ago
Job description
Senior CRA (FSP Global Biotech): Home-based in Wellington (preferred) or Auckland. ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Role: Senior CRA Location: Wellington/ Auckland (New Zealand) As a Senior Clinical Research Associate, you will be joining the world's largest & most comprehensive global biotech company with a strong track record in delivering high-quality clinical trials. You will be responsible for managing and coordinating clinical trial activities, ensuring compliance with regulatory requirements, and providing expert guidance to study teams. Your expertise will be instrumental in driving the success of our clients' programs. Key responsibilities: • Manage and coordinate clinical trial activities, including site initiation visits, monitoring visits, and close-out visits. • Ensure compliance with regulatory requirements, including GCP, ICH, and local regulations. • Provide expert guidance to study teams on clinical trial protocols, procedures, and best practices. • Collaborate with cross-functional teams to develop and implement effective clinical trial strategies. • Develop and maintain strong relationships with clients, investigators, and other stakeholders. • Stay up-to-date with industry trends, regulatory changes, and new technologies that impact clinical trials. What we're looking for: • Bachelor's degree in a life science or related field (or equivalent experience). • At least 5 years of experience as a CRA or similar role. • Strong understanding of GCP, ICH, and local regulations. • Excellent communication, interpersonal, and problem-solving skills. • Ability to work independently and as part of a team. • Strong attention to detail and organizational skills. Benefits: • Competitive salary and benefits package. • Opportunities for professional growth and development. • Collaborative and inclusive work environment. • Flexible working arrangements (home-based or office-based). • Access to cutting-edge technology and tools.
Required skills
- industry trends
- gcp
- best practices
- cross-functional teams
- regulatory compliance
- client relationships
- clinical research associate
- ich
- clinical trials
- procedures
- regulatory changes
- new technologies
- cra
- monitoring visits
- study teams
- clinical trial protocols
- site initiation visits
- icon plc
- senior cra
- fsp global biotech
- close-out visits
- investigator relationships
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