SharePoint Consultant

🕒 August 13

🏄 California – Remote

🏄 California – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

💼 Consultant

👻 Ghost score 38%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 91 days.
• No salary listed.

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BigHat Biosciences

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BigHat Biosciences is a biotechnology company focused on designing safer, more effective antibody therapies using machine learning and synthetic biology. The company leverages its Milliner platform, which integrates a high-speed wet lab with state-of-the-art machine learning technologies, to discover and engineer antibodies for intractable diseases like infections and cancers. Their approach promises to deliver next-generation therapies with improved safety and efficacy. Based outside San Francisco, BigHat Biosciences engages in strategic collaborations and partnerships to enhance their therapeutic programs and has raised significant funding to pursue these innovative solutions.

📋 Description

• Design and build SharePoint program management landing pages for documentation, risk communications, and action items • Integrate Smartsheet outputs or data feeds into SharePoint splash pages for real-time visibility into program risks and actions • Configure SharePoint and Power Automate document control workflows for IND-related regulatory submissions • Build automated review and adjudication routing for IND chapter documents submitted to FDA or ex-US health authorities • Configure access controls and library permission structures for regulated drug development • Provide SharePoint site administration, troubleshooting, and user access management throughout the engagement • Lead knowledge transfer and handoff to internal stakeholders upon project completion • Optionally assess and recommend Microsoft 365 Copilot or SharePoint AI agent features

🎯 Requirements

• Demonstrated experience designing and building SharePoint sites for program management, ideally in biotech, pharma, or regulated health sciences • Proficiency in Power Automate workflow configuration within SharePoint • Hands-on experience with document control systems and regulated document lifecycle management, including IND authoring pipelines or FDA submission workflows • Working knowledge of SharePoint access controls, library permissions, and compliance-aware configuration • Experience in clinical or drug development operational settings strongly preferred • Ability to work independently and manage deliverables across a remote engagement • Ability to communicate clearly with non-technical stakeholders • Collaborative, solution-oriented approach and comfort operating in a fast-moving startup environment • Must be based in the United States

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