Lead planning, conduct, and oversight of operational clinical studies per protocol.
Ensure studies comply with ICH-GCP, SOPs, and regulatory requirements.
Develop study documents, training materials, and trackers.
Drive site feasibility, recruitment strategies, and enrollment plans.
Manage IP handling, drug accountability, and QA coordination.
Lead cross-functional teams; monitor metrics and CAPA.

🎯 Requirements

Bachelor’s degree in science/health; advanced degree preferred.
7+ years of clinical research experience with monitoring.
Excellent communication, interpersonal and organizational skills.
MS Office proficiency (Outlook, Word, Excel, PowerPoint).
Deep knowledge of ICH-GCP and regulatory guidelines.
Willingness to travel domestically and internationally.

🎁 Benefits

Discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Paid time off for sick leave and vacation

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