Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is seeking a Contract CMC Technical Writer to critically review data, batch records, and development reports from external CDMOs to finalize source documents for analytical, drug substance and drug product.

The ro ...Read more

Paycom seeks a Source Creation Specialist to ensure accuracy and regulatory compliance of study source documents across trials. You will design, develop, and maintain study-specific sources, supporting quality control and inspection readiness in a fully remote role.

Responsibilities include ...Read more

Actalent is seeking a Fully Remote Clinical Documentation Specialist to improve documentation quality across care teams. You will perform concurrent and retrospective reviews, educate providers, and ensure regulatory compliance while collaborating with physicians, nurses, and other caregivers.

Adventist HealthCare seeks to hire a Clinical Documentation Specialist who will embrace our mission to extend God’s care through the ministry of physical, mental and spiritual healing.

Responsibilities

• Examine medical records to ensure documentation is accurate, complete, and ...Read more

Adventist HealthCare seeks a Clinical Documentation Specialist to ensure accurate documentation reflecting patient status across inpatient encounters. You will collaborate with physicians and staff to clarify documentation and support proper coding for reimbursement.

Responsibilities includ ...Read more

Adventist HealthCare seeks a Clinical Documentation Specialist to extend God’s care through a ministry of healing. The role focuses on reviewing medical records to ensure accurate documentation reflecting patient status, and educating staff to improve quality and compliance.

Responsibilit ...Read more