Global Clinical Trial Leader (Hybrid)

Dawar Consulting, Inc.; South San Francisco (CA); On-site; USD 81,000 - 99,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Paid Sick Leave

401K

Job summary

JobRx, Inc. is looking for a Global Clinical Trial Leader based in South San Francisco, CA. In this hybrid position, you will support global Phase I and II clinical trials, providing operational leadership and collaborating with cross-functional teams.

Qualified candidates should possess a Bachelor's degree and have over 8 years of clinical study management experience in the biotech or pharma industry. Benefits include medical, dental, vision, and a 401K plan.

Qualifications

• 8+ years of clinical study management experience in pharma, biotech, or CRO.
• Experience with global Phase I and II clinical trials.
• Strong vendor and CRO management experience.

Responsibilities

• Provide operational leadership to Protocol Execution Teams.
• Drive delivery of trial deliverables including documentation.
• Manage CROs and vendors to ensure performance aligns with expectations.

Skills

Clinical study management

Vendor management

GCP knowledge

Cross-functional collaboration

Education

Bachelor's degree in scientific or healthcare-related discipline

Job description

Job Description

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

• Provideoperational leadership and guidance to global cross-functional ProtocolExecution Teams (PETs) across study start-up, conduct, and close-outactivities.
• Drivedelivery of key trial deliverables including vendor specifications, drugsupply forecasting, monitoring plans, TMF, and CTMS documentation.
• Collaboratewith cross-functional stakeholders on study planning, protocolfeasibility, site selection, and investigator meetings.
• ManageCROs and vendors to ensure performance aligns with contracted scope,timelines, quality, and budget expectations.
• Contributeto study budget planning and oversee assigned vendor budgets.
• Identifyoperational risks, develop mitigation strategies, and proactively managestudy timelines and issues.
• Supportprocess improvement initiatives and contribute to clinical operations bestpractices.
• Mentorjunior team members and serve as a subject matter expert for designatedinitiatives.

Qualifications

• Bachelor'sdegree required; scientific or healthcare-related discipline preferred.
• 8+years of clinical study management experience within the pharmaceutical,biotech, or CRO industry.
• Experiencesupporting global Phase I and/or Phase II clinical trials.
• Strongvendor and CRO management experience.
• Workingknowledge of GCP, ICH guidelines, international regulations, and the drugdevelopment 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.

Contact

If interested, please send us your updated resume to [e-mail] or [e-mail].