SharePoint Consultant

BigHat Biosciences; United States; Remote; USD 111,000 - 185,000; Part time

Job summary

BigHat Biosciences is seeking an experienced SharePoint Development Consultant to design, build, and configure program management infrastructure for our drug development organization. This is a remote, project-based contract engaging with Operations and Program Management teams to streamline document review and approvals for regulated workflows.

You will develop landing pages, automate workflows with Power Automate, and implement access controls suitable for IND submissions, FDA-related

Qualifications

• Experience designing SharePoint sites for program management in biotech or regulated health sciences.
• Hands-on Power Automate configuration within SharePoint.
• Familiarity with IND authoring pipelines or FDA submission workflows.
• Knowledge of access controls and regulatory compliance in document management.

Responsibilities

• Design and build SharePoint program management landing pages for cross-functional stakeholders.
• Integrate Smartsheet data feeds into SharePoint pages for real-time risk visibility.
• Configure document control workflows with authors, reviewers, and adjudicators for IND submissions.
• Create automated review and adjudication routing for IND documents.
• Manage access controls and library permissions in a regulated environment.
• Provide SharePoint site administration and knowledge transfer at project end.

Skills

SharePoint development

Power Automate

Smartsheet integration

Document control workflows

IND/FDA submission workflows

Access controls & security

Remote collaboration

Tools

Smartsheet

Job description

The role: BigHat Biosciences is looking for an experienced and detail-oriented SharePoint Development Consultant to support the design, build-out, and configuration of SharePoint-based program management infrastructure for our drug development organization. This is a project-based contract engagement, performed remotely through project completion. The consultant will partner directly with our Operations and Program Management teams to build document control workflows, program-facing SharePoint sites, and Power Automate automations that replace manual, email-based document review and adjudication processes. This work will have a particular focus on cGXP documents, IND-related workflows, and regulatory submission processes.

Key Responsibilities

• Design and build SharePoint program management landing pages that surface program documentation, risk communications, and action items for cross-functional stakeholders
• Integrate Smartsheet outputs or data feeds into SharePoint splash pages to support real-time, redundant visibility into program risks and actions
• Configure document control workflows using SharePoint and Power Automate, including assignment of document authors, reviewers, and adjudicators for IND-related regulatory submissions
• Build automated review and adjudication routing for IND chapter documents (e.g., modules submitted to FDA or ex-US health authorities), replacing manual email-based review chains
• Configure access controls and library permission structures appropriate for a regulated drug development environment
• Provide SharePoint site administration support - including troubleshooting and user access management - on an as-needed basis throughout the engagement
• Lead knowledge transfer and handoff to internal stakeholders upon project completion
• Optionally: assess and recommend opportunities to incorporate Microsoft 365 Copilot or SharePoint AI agent features

Skills Knowledge and Expertise

• Demonstrated experience designing and building SharePoint sites for program management use cases, ideally in a biotech, pharma, or regulated health sciences environment
• 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, manage deliverables across a remote engagement, and communicate clearly with non-technical stakeholders
• A collaborative, solution-oriented approach and comfort operating in a fast-moving startup environment
• Must be based in the United States