Clinical Data Programmer for EDC System

About

Clora's client is a clinical-stage biopharma company developing precision medicines to redefine the treatment of serious diseases across oncology, neurology, and immunology.

Responsibilities

• Program the initial edit checks for 1 clinical trial for the client's EDC system, Medidata RAVE (approx. 600-800 edit checks)
• Triage client's feedback during UAT and address updates
• Potential for future ongoing EDC updates and EDC builds
• Collaborate with client's internal clinical team and CRO partners

Ideal Candidate

• 7+ years in clinical programming for sponsor companies. Biotech/Pharma experience preferred.
• Ideal candidate should have a strong background in Clinical Programming with experience in Medidata RAVE. Responsibilities include overseeing database builds, creating edit checks, and ensuring adherence to industry standards to support clinical trials.
• Comfortable working in a fast-paced environment, be an efficient and independent problem solver, and be able to make and communicate decisions effectively.
• Oncology experience is preferred.

Skills

• Functional Areas
• Data Management - Must have

Therapeutic Areas

• Oncology

Development Phases

• I/Exploratory
• II/Proof of Concept

Regulatory Pathways

• IND