Location & Working Model: Hybrid, South San Francisco, CA (Three days in office, Two days remote)<\/span><\/span><\/b><\/span>
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Job Duration: Long Term Contract (Possibility Of
Extension)<\/span><\/span><\/b><\/span>
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Pay Rate : $81/hr on W2 DOE<\/span><\/span><\/b><\/span>
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Company Benefits:<\/span><\/span><\/b> Medical, Dental, Vision, Paid Sick leave, 401K<\/span><\/span><\/span>
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The Clinical Operations Lead<\/b> supports
the execution and delivery of global clinical trials within a cross -functional,
matrixed clinical development organization. This role collaborates with global
teams to drive operational activities that support study delivery, improve
clinical trial processes, and enhance patient, investigator, and site
experiences.<\/span><\/span><\/span><\/span>
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Key Responsibilities<\/span><\/span><\/span><\/u><\/b><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Support
operational execution of clinical trials and development programs<\/b> across
disease areas.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Provide operational
and strategic input<\/b> to cross -functional study teams.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Collaborate
with global stakeholders to support study management, process improvements,
and clinical operations initiatives<\/b>.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Ensure
compliance with ICH, GCP, and regulatory guidelines<\/b> and maintain high
standards of data integrity.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Partner
with investigators and clinical sites to strengthen relationships and improve
trial delivery.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Contribute
to innovation, digital adoption, and continuous improvement initiatives<\/b> within clinical operations.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Support
global and local initiatives aligned with clinical development priorities.<\/span><\/span><\/span><\/span>
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Qualifications<\/span><\/span><\/span><\/u><\/b><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>2–5 years
of experience<\/span><\/span><\/span><\/b><\/span> in clinical
operations, drug development, or related field<\/b>.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Knowledge
of clinical trial processes and regulatory guidelines (ICH/GCP)<\/b>.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Strong
organizational, problem -solving, and communication skills.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Ability to
collaborate across cross -functional and global teams<\/b> in a dynamic
environment.<\/span><\/span><\/span><\/span>
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· <\/span><\/span><\/span><\/span><\/span><\/span>Experience
supporting clinical studies, enabling projects, or operational initiatives<\/b> preferred.<\/span><\/span><\/span><\/span>
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If interested, please send us your updated resume at<\/span><\/span><\/span>
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hr@dawarconsulting.com
akansha@dawarconsulting.com
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