Senior Director, Clinical Trial Documents & Insights

WCG Clinical, Inc.; Lansing (MI); Remote; USD 120,000 - 186,000; Full time

Benefits offered by this job

Healthcare and dental insurance

401(k) with company match

Tuition reimbursement

Certification assistance

Continuing education support

Paid holidays and vacation

Job summary

WCG is seeking a Senior Director, Clinical Trial Document Authoring & Insights to lead an innovative team at the forefront of clinical trial document authoring and analytics. You will translate protocol knowledge into product requirements, working prototypes, and differentiated solutions for sponsors, CROs, and sites.

The role combines clinical science, technology, and commercial strategy in a fast-moving environment, demanding autonomy, strategic thinking, and strong stakeholder influence

Qualifications

• 8+ years of experience in healthcare, life sciences, clinical research, or a similarly complex, regulated industry
• Leadership role in product, engagement, or domain leadership is required
• Direct experience with clinical trial protocols and study documentation is preferred

Responsibilities

• Lead a team of domain and analytical professionals with clear objectives and accountability
• Partner with Product Management and Engineering across the development lifecycle
• Define problem sets, maps workflows, and prioritize opportunities with commercial impact
• Develop and test prototypes, models, and pilot offerings with measurable results
• Represent WCG in industry conferences and client-facing activities

Skills

Leadership

Cross-functional collaboration

Structured problem solving

Executive communication

Hands-on execution

Applied AI/LLMs knowledge

Education

Bachelor's degree or higher

Advanced degree preferred

Clinical research certifications preferred

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

WCG is seeking a Senior Director, Clinical Trial Document Authoring & Insights to lead an innovative team at the forefront of clinical trial document authoring and analytics. You will translate protocol knowledge into product requirements, working prototypes, and differentiated solutions for sponsors, CROs, and sites.

The role combines clinical science, technology, and commercial strategy in a fast-moving environment, demanding autonomy, strategic thinking, and strong stakeholder influence