Invences Consulting

Clinical Research

• Participate fully in the 8-week CRA Training Program, including structured learning, functional rotations, and assessments
• Participate in coaching and mentoring with Line Managers, cross-functional stakeholders, the assigned Senior CRA mentor, and graduate cohort peers
• Support supervised site management activities, including maintaining essential site documentation and Investigator Site Files
• Assist with Trial Master File coordination, document filing, quality checks, and completeness
• Support preparation for monitoring visits, participate in co-monitoring or observational visits, and complete routine follow-up activities under guidance
• Support data review, query resolution, and maintenance of clinical trial systems such as CTMS, eTMF, and eCRF
• Provide in-house support to clinical trial teams, internal teams, sites, and vendors on assigned studies
• Assist with study administration, including basic finance, regulatory, safety, and study close-out support
• Apply Novotech quality standards, ICH GCP, and regulatory requirements; promptly escalate risks, issues, and safety concerns
• Adhere to company processes and assist in reviewing and developing clinical SOPs and processes
• Maintain professional internal and external communications reflecting Novotech’s company image
• Progress toward CRA I and subsequently CRA II subject to performance, readiness, and successful training completion

Explore Graduate Clinical Research Associate, CRA at Invences Consulting. Review requirements and application details.

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Graduate Clinical Research Associate, CRA