← all jobs

Clinical Data Programmer for EDC System

Work from home Full-time role Hiring

Logistics Manager; Director Level 40 hours per week for 2 months Remote, ideally from Watertown, MA preferred, or EST-based Travel Requirements: N/A Hourly rate: $85 - $150 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. The Client is looking for a Clinical Database EDC Programming consultant with proven expertise in Medidata RAVE. For the initial scope of this project, this consultant will set-up and program all of the data validation edit checks (600-800 edit checks) for 1 study. While this project will be billed hourly (actuals / Time & Materials), the consultant should anticipate 7 weeks for approx. 250 hrs in total. These estimated hours are subject to fluctuations based on the final number of edit checks and complexity of each edit check. Client anticipates a programming edit checks phase (~5 weeks), a Client's user acceptance testing phase (~1 week), and an updates phase (~1 week). This 7-week contract opportunity has the potential to extend, subject to project demands and mutual interest.

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.

More open positions

Clinical Research Data and Analytics Manager (Hybrid)

Work from home Full-time role

Associate Director, Governance & Data Management Operations Enablement, IQVIA Digital (Remote)

Work from home Full-time role

Data Manager (Permanent role )

Work from home Full-time role

Lead Clinical Data Analyst

Work from home Full-time role

Clinical Trials Research Asst/Data Manager - Children's Oncology Group

Work from home Full-time role

Senior Client Solutions Manager, Performance Advertising

Work from home Full-time role

Internal Audit Professional

Work from home Full-time role

Art Director

Work from home Full-time role

Prior Authorizations Specialist- Urology (Remote)

Work from home Full-time role

[Remote] Forward Deployed Engineer (FDE) - GenAI + Agentic AI

Work from home Full-time role

2027 Audit or Tax Entry Level Staff

Work from home Full-time role

Partner Solutions Engineer

Work from home Full-time role

Manual QA Engineer – Middle/Senior

Work from home Full-time role

GESTOR/A PERSONAL A DISTANCIA - CONNECTA - DT - PERSONAL - CONTRIBUIDOR INDIVIDUAL

Work from home Full-time role

Field Reimbursement Manager, Southwest

Work from home Full-time role

Multi-Site Construction Manager – Structures

Work from home Full-time role

[Remote] Dir GPO & Account Management - South Cetnral

Work from home Full-time role

Fully Remote Data Entry Clerk – Precision Database Management, Reporting & Process Optimization

Work from home Full-time role

Experienced Full Stack Senior Program Manager – Digital Customer Success & Experience

Work from home Full-time role

Experienced Remote Social Media Strategist - No Experience Required - Earn $35/hr!

Work from home Full-time role

Safety Specialist – Field Operations

Work from home Full-time role