Senior Clinical Research Associate
On-siteBuenos Aires, Buenos Aires F.D., Argentina
Job Summary
Manage research activities at sites participating in Worldwide's clinical research projects, including identifying potential sites, performing study start-up activities, and training sites to collect data properly. Conduct study initiation visits (SIVs) to ensure compliance with informed consent and safety reporting while adhering to regulatory requirements. Handle site activities during study maintenance and close down research activities once the study concludes. Requires 5+ years of experience as a Clinical Research Associate, an Oncology background, and proficiency in CTMS and EDC systems. Candidates must reside in Argentina and be willing to travel regionally.
Required Qualifications
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC Systems
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Oncology
- Fluent in written and verbal English
- Candidates must reside in Argentina
- Willingness to travel regionally
Desired Qualifications
- Rare Disease experience
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