Monitor budgets and financial metrics for clinical trials.

Manage site activation and regulatory submission processes.

Manage site activation and regulatory submission processes.

Support product launches and scientific engagement.

Analyze and validate clinical data from ongoing trials.

Perform safety assessments and regulatory submissions.

Lead global clinical trial projects and manage budgets/timelines.

Conduct audits and ensure quality standards in clinical research.

Provide administrative support to clinical project teams.

Provide statistical support for clinical trial design and analysis.

Monitor, assess, and report adverse drug reactions.

Oversee data collection, integrity, and analysis for clinical studies.

Ensure products meet regulatory standards before market launch.

Prepare scientific documents for regulatory submission and publication.

Coordinate and manage clinical trials and ensure regulatory compliance.