Our project management team is experienced in early-phase clinical trial planning and management. We ensure efficient coordination and monitoring of clinical trials based on an integrated approach. Our teams implement plans through to proof-of-concept/phase II, including: investigator and clinical research unit identification, qualification, and selection; study protocol writing and review; case report form design; coordination of clinical trial applications; budgeting and budget management; risk management; study oversight; supervision, coordination and follow-up of SAEs during study conduct; coordination with data management teams, bioanalytical laboratories and other partners; and clinical study report writing and review.

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