Remote Data Jobs · CDISC

• Oversee clinical trial data management from start to lock.
• Develop CRF specs and manage database build validation.
• Coordinate medical coding and SAE reconciliation with vendors.

• Lead statistical programming activities for Phase I–IV clinical studies across therapeutic areas.
• Develop and maintain CDISC-compliant SDTM and ADaM specifications and SAS programs.
• Mentor junior programmers and ensure regulatory compliance for submissions.

The partner company is a clinical research organization focused on driving healthcare innovation through clinical trials. The company's size and culture are not specified in the posting.

• Lead the development, execution, and evolution of the Clinical Data Management function.
• Build and mentor a high-performing team while establishing SOPs, governance, and inspection-ready practices.
• Oversee data management activities across clinical studies, ensuring high-quality, regulatory-compliant data delivery.

Dianthus Therapeutics is a biotechnology company developing best-in-class therapies for patients with severe autoimmune diseases. It is a growing organization with a culture centered on core principles and patient care.

• Participate in CRF design, database review, and data validation procedures to ensure data integrity.
• Produce data listings, summary tables, and graphics for interim and final analyses of clinical trials.
• Collaborate with Biometrics functions and coordinate data transfer standards with CROs and vendors.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, they maintain a supportive culture focused on quality, professional development, and low turnover.

• Develop, validate, and maintain SAS and/or R programs for SDTM, ADaM datasets, and TLFs per CDISC standards.
• Support statistical analyses for regulatory submissions, safety reports, and clinical study reports in a GxP-compliant environment.
• Collaborate with cross-functional teams to define analysis specifications and perform quality control on statistical outputs.

Iovance Biotherapeutics is a global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) therapy for cancer. The company is a fast-paced biotech with a collaborative culture, committed to continuous innovation in cell therapy.

• Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
• Support TLF generation in R or SAS as needed for clinical trial deliverables.
• Collaborate with biostatistics and clinical data teams to ensure regulatory compliance and quality.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies. They have over 4,000 professionals in more than 20 countries and emphasize a culture of low turnover, diversity, and inclusivity.