Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
6 days ago
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
• Site Monitor responsible for data integrity, quality, and compliance. • Conducts monitoring activities in line with Study Monitoring Plan (SMP). • Collaborates with Site Manager and site personnel.
• Networking and relationship building skills. • Ability to communicate effectively and appropriately with internal and external stakeholders. • Ability to adapt to changing technologies and processes. • Effectively overcoming barriers encountered during the implementation of new processes and systems. • Excellent communication (verbal and written), presentation, and interpersonal skills relating to colleagues and associates, both inside and outside of the organization. • Identifies and builds effective relationships with investigator site staff and other stakeholders. • Proficiency in local language is required. • Advanced level or fluency in English is required.
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