Senior Clinical Research Associate
On-siteJohannesburg, Gauteng, South Africa
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams to guarantee timely data collection and reporting while providing training to site staff and other CRAs. Build effective relationships with site personnel and stakeholders to facilitate smooth operations. Requires a Bachelor's degree, minimum 5 years CRA experience including oncology and Phase I studies, and willingness to travel approximately 60%. Join ICON to help deliver new medicines and medical devices benefiting patients worldwide.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Minimum of 5 years' experience as a Clinical Research Associate
- Experience monitoring oncology clinical trials
- Ideally Phase I studies
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices
- Data integrity
- Site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
Desired Qualifications
- Ideally Phase I studies
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