Offer summary
Qualifications:
Bachelor's degree in life science/related field, Minimum of 3+ years in clinical research, Solid understanding of GCP and regulatory requirements, Excellent organizational and communication skills, Interpersonal skills to work in a team.
Key responsabilities:
- Participate in study protocol review and development
- Assist in site selection and qualification process
- Conduct training and site initiation visits
- Perform monitoring visits and data verification
- Communicate regularly with study sites and stakeholders