Offer summary
Qualifications:
Bachelor's degree in Nursing, Life Sciences, or Medical Sciences, Previous Clinical Research Associate experience, Familiarity with CTMS, eTMF, IXRS, and EDC systems, Knowledge of regional clinical research regulations and ICH-GCP.
Key responsabilities:
- Manage study site activities and essential document collection
- Conduct site visits in adherence to SOPs/WPDs
- Prepare accurate visit reports and lead observational visits
- Collaborate with project functional leads, mentor less experienced CRAs