Plan, direct, coordinate, and deliver clinical study projects on time and within budget.
Serve as primary client contact and escalation point.
Coordinate external vendors to the established timeline and budget.
Manage study budget and profitability; flag out-of-scope work.
Develop robust project plans, timelines, and proactive risk mitigation.
Ensure quality management, eTMF readiness, and regulatory compliance.

🎯 Requirements

Bachelor's degree in science/health field; advanced degree preferred.
Minimum 7 years clinical research; at least 4 years PM experience.
Experience managing complex/global trials.
Strong cross-functional management and risk/change planning.
Proficiency with PM software (e.g., MS Project, CTMS).
Oncology or cell/gene therapy experience preferred.

🎁 Benefits

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

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