Senior Director - CT Document Authoring & Insights (Remote)
WCG Clinical, Inc.
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Benefits offered by this job
Job summary
WCG Clinical, Inc. is seeking a Senior Director, Clinical Trial Document Authoring & Insights. You will lead a cross‑functional team shaping next‑gen document authoring and analytics for trials, translating protocols into market-ready capabilities.
The role blends clinical science, technology, and commercial strategy with autonomous, high‑impact leadership. You will drive hypotheses, validate findings with clients, and deliver artifacts that accelerate sponsor, CRO, and site documentation
Qualifications
- 8+ years in healthcare, life sciences, or regulated industry with leadership experience.
- Direct experience with clinical trial protocols and study documentation is strongly preferred.
- Proven ability to lead cross-functional initiatives without direct authority.
Responsibilities
- Lead a team in defining, developing, and commercializing clinical trial document authoring capabilities.
- Translate client needs into actionable product requirements and roadmaps.
- Partner with Product Management and Engineering through full development lifecycle.
- Establish quality standards, benchmarks, and regulatory defensibility for outputs.
- Represent WCG in industry forums and drive continuous improvement initiatives.
Skills
Education
Tools
Job description
WCG Clinical, Inc. is seeking a Senior Director, Clinical Trial Document Authoring & Insights. You will lead a cross‑functional team shaping next‑gen document authoring and analytics for trials, translating protocols into market-ready capabilities.
The role blends clinical science, technology, and commercial strategy with autonomous, high‑impact leadership. You will drive hypotheses, validate findings with clients, and deliver artifacts that accelerate sponsor, CRO, and site documentation
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