Remote Senior Director CT Document Authoring & Insights

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

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) match

Flexible spending accounts

Employee assistance programs

Work-life balance tools

Tuition reimbursement

On-the-job training

Certification assistance

Continuing education

Paid holidays

Vacation days

Sick time

Career development

Job summary

WCG Clinical, Inc. is seeking a Senior Director to lead a team at the forefront of clinical trial document authoring and analytics.

You will translate deep domain knowledge into product requirements, prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design, author, and review trial documents. The role combines strategic guidance with hands-on execution, requiring rapid hypothesis validation with clients and internal experts, and collaboration across Product

Qualifications

• 8+ years in healthcare or life sciences.
• Leadership experience in a complex, regulated environment.
• Direct experience with clinical trial protocols and study documentation is preferred.
• Strong written and verbal communication; executive-level deliverables.

Responsibilities

• Lead a team of domain and analytical professionals to deliver protocol optimization outputs.
• Translate client needs into actionable product roadmap and priorities.
• Partner with Product Management and Engineering through the development lifecycle.
• Define quality standards, evaluation criteria, and benchmarks for new capabilities.
• Represent WCG in industry conferences, webinars, and thought leadership.

Skills

Leadership

Clinical research

Cross-functional collaboration

Strategic thinking

Communication

Regulatory submission

Problem solving

AI in regulated contexts

Education

Bachelor's degree or higher

Advanced degree preferred

Job description

WCG Clinical, Inc. is seeking a Senior Director to lead a team at the forefront of clinical trial document authoring and analytics.

You will translate deep domain knowledge into product requirements, prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design, author, and review trial documents. The role combines strategic guidance with hands-on execution, requiring rapid hypothesis validation with clients and internal experts, and collaboration across Product