Sr. CRA 3, Argentina, IQVIA Biotech
On-siteBuenos Aires, Buenos Aires F.D., Argentina
Job Summary
Independently manage and monitor clinical trial sites to ensure compliance with protocols, GCP, ICH guidelines, and regulatory requirements. Perform site qualification, initiation, routine monitoring, and closeout visits while partnering with investigative sites to support patient recruitment and retention. Provide protocol training, resolve data queries, oversee site performance, and document monitoring activities through accurate reports. Collaborate with cross-functional teams to support trial execution and mentor junior CRAs via co-monitoring and training. Requires a Bachelor's degree and minimum 4 years of on-site clinical monitoring experience.
Required Qualifications
- Bachelor's degree in a scientific, healthcare, or related discipline (or equivalent combination of education and experience)
- Minimum of 4 years of on-site clinical monitoring experience
- Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes
- Experience conducting monitoring visits across multiple phases of clinical research
- Excellent organizational, communication, and problem-solving skills
- Ability to effectively manage multiple priorities in a fast-paced environment
- Proficiency with Microsoft Office applications and clinical trial systems
Desired Qualifications
- Strong therapeutic area knowledge and protocol management experience
- Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams
- Experience mentoring or supporting the development of junior clinical research professionals
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