Senior Director, CT Document Authoring & Insights (Remote)

WCG Clinical, Inc.; Trenton (NJ); 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) matching

Flexible spending accounts

Employee assistance program

Work-life balance support

Referral bonuses

Tuition reimbursement

On-the-job training

Certification assistance

Continuing education support

Paid holidays

Vacation time

Sick time

Career development opportunities

Job summary

WCG Clinical, Inc. is seeking a Senior Director of Clinical Trial Document Authoring & Insights to lead a talented team at the forefront of protocol development and analytics.

You will translate deep domain knowledge into product requirements, work prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design and review trial documents. The role operates with high autonomy in a fast-moving environment, requiring strategic thinking, client validation, and hands-on

Qualifications

• 8+ years in healthcare or life sciences with leadership experience.
• Direct experience with clinical trial protocols and study documentation preferred
• Excellent written and verbal communication; able to produce executive-level deliverables.

Responsibilities

• Lead domain and analytics efforts for clinical trial document authoring solutions.
• Partner with Product Management and Engineering across ideation, design, and release.
• Define problem statements, assess workflows, and prioritize opportunities with commercial impact.
• Build prototypes and pilots to test feasibility and demonstrate value quickly.
• Lead a team of experts and ensure delivery of high-quality outputs.

Skills

Leadership experience

Clinical trial knowledge

Product management

Cross-functional collaboration

Strategic thinking

Education

Bachelor's degree or higher

Advanced degree preferred

Job description

WCG Clinical, Inc. is seeking a Senior Director of Clinical Trial Document Authoring & Insights to lead a talented team at the forefront of protocol development and analytics.

You will translate deep domain knowledge into product requirements, work prototypes, and differentiated solutions that improve how sponsors, CROs, and sites design and review trial documents. The role operates with high autonomy in a fast-moving environment, requiring strategic thinking, client validation, and hands-on