Leads global clinical research studies with a focus on study management, project oversight, and potential oncology programs.

Job Requirements:

15+ years of experience in clinical research

Extensive experience in global study management

Strong project management skills

Ability to operate effectively in a fast-paced environment

Preferred Skills:

Oncology clinical trial experience

Familiarity with regulatory requirements for global studies

Proficiency in managing cross-functional clinical teams

Experience with clinical trial systems and tools

Job Responsibilities:

Oversee end-to-end execution of global clinical trials

Manage study timelines, budgets, and deliverables

Coordinate with cross-functional teams and external vendors

Ensure regulatory compliance and adherence to study protocols

Provide strategic input into trial design, planning, and risk management

Pay Details: $81.00 to $108.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance ActLos Angeles City Fair Chance OrdinanceLos Angeles County Fair Chance Ordinance for EmployersSan Francisco Fair Chance Ordinance