Senior Source Creation

The Senior Source Creation Specialist ensures the accuracy and quality of research data by supporting quality control activities. The role is responsible for designing, developing, and maintaining study-specific source documents to ensure accuracy, regulatory compliance, and alignment with study protocols. The Senior Source Creation Specialist also provides oversight, training, and guidance to junior Source Creation Specialists, including review of their work.

This role is critical in supporting data integrity and inspection readiness.

JOB RELATIONSHIPS:

Reports directly to the Director of Strategy and Operations and indirectly to Regional Research Managers and the Finance Manager.

Collaborates with finance, sponsors, site staff, quality, and regional site managers.

Bachelor’s degree in life sciences, healthcare, or related field.
2–4 years of experience in clinical research, including source document creation.

Strong knowledge of GCP, FDA, and ICH requirements.

Excellent attention to detail and document management skills.

Complex specialty therapeutic area trial experience preferred. Ex:
Urology, Neurology, Endocrinology, etc.

Ability to collaborate across multiple teams and stakeholders.

Understanding of clinical trial budgets and how they relate to source documentation creation in a CTMS system.

Exceptional time management skills and the ability to prioritize varying trial recruitment timelines.

Excellent communication skills and the ability to interact with all levels of management, staff, vendors, sponsors, and providers.

ESSENTIAL JOB RESPONSIBLITIES:

Provide day-to-day oversight of junior Source Creation Specialists, including assigning and prioritizing work, reviewing source documents for accuracy and completeness, and providing feedback before release.

Train and mentor junior Source Creation Specialists on source development standards, study document review, version control, and quality checks; identify knowledge gaps and provide ongoing guidance.

Review study protocols and create compliant source documents tailored to each protocol for all research trials in each company market.

Collaborate with study teams, investigators, and coordinators to ensure usability of source forms.

Ensure that all source documents meet sponsor, IRB, and regulatory requirements.

Update and revise source templates based on protocol amendments or feedback.

Maintain version control and archiving of all source documents.

Train site staff on correct use of source documents to ensure accurate data capture.

Support audits and inspections by providing well-documented, compliant source materials.

Collaborate with finance to ensure all invoiceable are correctly tied to source within the CTMS system.

Participate in study kick off calls to communicate source development efforts and train site staff on source specifics.

Collaborate with site staff and site managers to ensure protocol updates and all up to date eCRF guidelines are available for use in a timely manner.

Proactively roll out source post protocol amendment and ensure site staff is aware of source updates.

Work alongside finance to review and/or create budget templates within the CTMS system to support source creation.

Follows up with staff to resolve internal data queries within the CTMS as needed.

Updates source documents as updates to protocols occur and errors are found.

Support with analyzing quality data to determine areas of growth and improvement.

Supports strategy to improve quality across all markets.

Facilitates ongoing training and shadows visits as needed for eSource use and quality improvement.

Other duties as assigned.

PERFORMANCE REQUIREMENTS:

Knowledge Knowledge of clinical research in a specialty setting; clinical research software, and sponsor requirements for…