Remote Protocol Intelligence Lead

WCG Clinical, Inc.; Helena (MT); Remote; USD 120.000 - 186.000; Vollzeit

Benefits dieser Stelle

Health insurance

401(k) with company match

Tuition reimbursement

Continuing education support

Zusammenfassung

WCG Clinical, Inc. seeks a Senior Director, Clinical Trial (CT) Document Authoring & Insights to lead a team at the forefront of defining and delivering next‑gen trial documents and analytics.

You will translate deep domain knowledge into requirements, prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design and review trial documents. You will drive collaboration across Product Management, Engineering, and Business Development, manage senior stakeholders,

Qualifikationen

• 8+ years in healthcare, life sciences, or regulated industry with leadership experience.
• Bachelor's degree or higher required; advanced degree preferred.
• Experience with clinical trial protocols, study documentation, and regulatory workflows is highly desirable.

Aufgaben

• Define problem sets and map current authoring and review workflows across sponsors, CROs, and sites.
• Translate client needs into actionable recommendations for roadmap and priorities.
• Lead domain experts to deliver protocol optimization and documentation outputs.
• Partner with Product Management and Engineering throughout development lifecycle.
• Build prototypes and pilots to demonstrate feasibility and value quickly.
• Represent the domain in client discussions and pursuit work.

Kenntnisse

Leadership

Strategic thinking

Cross-functional collaboration

Structured problem solving

Executive communication

Hands-on execution

Ausbildung

Bachelor's degree or higher

Advanced degree preferred

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Jobbeschreibung

WCG Clinical, Inc. seeks a Senior Director, Clinical Trial (CT) Document Authoring & Insights to lead a team at the forefront of defining and delivering next‑gen trial documents and analytics.

You will translate deep domain knowledge into requirements, prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design and review trial documents. You will drive collaboration across Product Management, Engineering, and Business Development, manage senior stakeholders,