Sr. Clinical Research Associate
EyeBio
Job Description
CORE Competency Expectations:
Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively.
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices.
Demonstrated ability to mentor/lead and/or Capable of mentoring junior CRAs on process/study requirements and is able to perform co-monitoring visits where appropriate.
Experience and Educational Requirements:
Bachelor’s degree, certificate or equivalent in a scientific / healthcare discipline together
4 years of direct site management (monitoring) experience in bio / pharma / CRO.
Required Skills:
Accountability, Clinical Site Management, Clinical Study Management, Clinical Trials Monitoring, Good Clinical Data Management Practice (GCDMP), Patient Recruitment, Protocol Adherence, Regulatory Affairs CompliancePreferred Skills:
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Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
RemoteShift:
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Job Posting End Date:
10/9/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.