Global Clinical Trial Leader (Hybrid)

Our client, a world
leader in biotechnology and life sciences, is looking for a "Global
Clinical Trial Leader" based out of South San Francisco, CA(Hybrid).

Job Duration: Long
Term Contract (Possibility Of Extension)

Pay Rate : $90/hr on W2

Company Benefits: Medical, Dental,
Vision, Paid Sick leave, 401K

Support the execution
and delivery of global Phase I and II clinical trials within Research and Early
Development (RED). Partner with cross -functional teams, vendors, and
stakeholders to ensure successful study execution, risk management, operational
excellence, and compliance with GCP/ICH and regulatory requirements.

Key Responsibilities:

• Provide
  operational leadership and guidance to global cross -functional Protocol
  Execution Teams (PETs) across study start -up, conduct, and close -out
  activities.
  
• Drive
  delivery of key trial deliverables including vendor specifications, drug
  supply forecasting, monitoring plans, TMF, and CTMS documentation.
  
• Collaborate
  with cross -functional stakeholders on study planning, protocol
  feasibility, site selection, and investigator meetings.
  
• Manage
  CROs and vendors to ensure performance aligns with contracted scope,
  timelines, quality, and budget expectations.
  
• Contribute
  to study budget planning and oversee assigned vendor budgets.
  
• Identify
  operational risks, develop mitigation strategies, and proactively manage
  study timelines and issues.
  
• Support
  process improvement initiatives and contribute to clinical operations best
  practices.
  
• Mentor
  junior team members and serve as a subject matter expert for designated
  initiatives.
  

Qualifications:

• Bachelor’s
  degree required; scientific or healthcare -related discipline preferred.
  
• 8+
  years of clinical study management experience within the pharmaceutical,
  biotech, or CRO industry.
  
• Experience
  supporting global Phase I and/or Phase II clinical trials.
  
• Strong
  vendor and CRO management experience.
  
• Working
  knowledge of GCP, ICH guidelines, international regulations, and the drug
  development process.
  

Preferred Experience:

·       Early
development clinical trial experience.

·       Global
study execution and operational strategy experience.

·       Experience
managing complex, multi -country clinical studies.

Travel:
Some travel may be required.

If interested, please
send us your updated resume at

[email protected]/[email protected]