Sr Dir or VP of Clin Ops
Company: ALLInBio, Inc.
Location: Stanford
Posted on: February 15, 2026
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Job Description:
Location Headquarters in Palo Alto, CA, USA. Company Overview We
are a clinical-stage biotechnology startup focused on developing
innovative therapies for patients with serious unmet medical needs,
with a primary focus on autoimmune diseases. We operate in a
fast-paced, highly collaborative environment and value
entrepreneurial individuals who thrive in building processes,
solving problems, and executing clinical trials hands-on. We
operate in a “virtual but local” manner. This implies that the
candidate can work from any place of their choice but must be
available to meet in person on a weekly basis at our headquarters
in Palo Alto, CA, USA. Role Summary We are seeking a Clinical
Operations professional with hands-on experience conducting global
clinical trials across the United States, United Kingdom, and
European Union. This role will be responsible for the end-to-end
execution of clinical studies, working closely with CROs,
investigators, vendors, and internal cross-functional teams. Prior
experience in autoimmune or immunology indications is strongly
preferred but not required. This role is ideal for someone who
enjoys wearing multiple hats and contributing directly to trial
execution in a startup environment. Key Responsibilities Clinical
Trial Execution Lead or support the planning, initiation,
execution, and close-out of clinical trials (Phase I–III) Manage
day-to-day clinical operations activities while ensuring timelines,
quality, and budget adherence Develop and maintain key trial
documents (e.g., protocols, ICFs, monitoring plans, TMF plans)
Vendor & CRO Management Select, manage, and oversee CROs and
vendors (e.g., monitoring, data management, labs) Review and
approve monitoring reports, metrics, and deliverables Serve as the
primary operational point of contact for external partners Global
Regulatory & Compliance Ensure trials are conducted in compliance
with ICH-GCP, FDA, MHRA, EMA, and local regulations Support
regulatory submissions and approvals in the US, UK, and EU (e.g.,
IND/CTA) Oversee Trial Master File (TMF) completeness and
inspection readiness Site Management Support site selection,
initiation, and ongoing site management Collaborate with
investigators and site staff to address enrollment, compliance, and
quality issues Identify and mitigate operational risks impacting
site performance Cross-Functional Collaboration Work closely with
Clinical Development, Regulatory Affairs, Data Management,
Biostatistics, Safety and Technical Operations Provide operational
input into protocol design, feasibility, and study budget and
timelines Contribute to process development and continuous
improvement in a startup setting Required Qualifications Bachelor’s
degree in life sciences or related field (advanced degree
preferred) 5 years of hands-on clinical operations experience
(flexible based on seniority) Direct experience managing clinical
trials in the US, UK, and EU Strong knowledge of ICH-GCP and global
clinical trial regulations Demonstrated ability to work
independently and manage multiple priorities Experience working in
a startup or small biotech environment Preferred Qualifications
Experience in autoimmune diseases, immunology, or inflammatory
indications Experience across multiple trial phases (Phase I–III)
Prior involvement in inspections or audits (FDA, EMA, MHRA) Ability
to build and improve clinical operations processes from the ground
up Key Competencies Hands-on, execution-focused mindset Strong
organizational and project management skills Excellent
communication and presentation skills and stakeholder management
abilities Proactive problem-solver comfortable with ambiguity
Team-oriented with a strong sense of ownership Why Join Us
Opportunity to make a direct impact on clinical programs and
patients High visibility and responsibility in a growing startup
Collaborative, science-driven culture Competitive compensation and
benefits
Keywords: ALLInBio, Inc., Antioch , Sr Dir or VP of Clin Ops, Science, Research & Development , Stanford, California