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Senior CRA / CRA II - Solid Tumor Direct Monitoring

syneoshealth · GRC-Remote

Νέο Remote
Remote Senior 🇬🇧 English
ICH-GCP Source Data Verification Electronic Data Capture Clinical Monitoring

Περιγραφή θέσης

About the role

Syneos Health is recruiting a Senior CRA/CRA II for a biopharmaceutical client, working on direct monitoring of solid tumor trials. The role is remote and requires proven experience with traditional on-site monitoring, including full source data verification, investigational product accountability and strict adherence to ICH/GCP and regulatory requirements.

Key responsibilities

  • Perform site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remotely), evaluating site performance and escalating serious issues
  • Verify informed consent, protect subject confidentiality and assess factors affecting safety and data integrity
  • Review source documents and medical records, verify CRF data accuracy and completeness, resolve queries and check compliance with electronic data capture
  • Check investigational product inventory, dispensing and administration, and ensure proper labelling, import and release/return
  • Review the Investigator Site File, reconcile it with the Trial Master File and document site activities
  • Support recruitment and retention, enter tracking data, prepare for investigator and sponsor meetings, and guide sites toward audit readiness
  • Train and mentor junior CRAs, including sign-off visits, and liaise with project site personnel

Required profile

  • Bachelor's degree or RN in a related field, or equivalent education, training and experience
  • Strong background in oncology clinical trials across all phases, including early-phase, first-in-human, safety, PK/PD and dose-escalation studies
  • Phase I oncology experience is essential
  • Hands-on experience with solid tumor indications (melanoma, breast, ovarian, prostate, lung cancer) and comfort in fast-paced development environments
  • English and German; multilingual capability
  • Able to travel regularly up to 75%

Required skills

  • Good Clinical Practice (ICH-GCP) knowledge and familiarity with ICH guidelines and other regulatory requirements
  • Good computer skills and willingness to adopt new technologies
  • Excellent communication, presentation and interpersonal skills, and basic critical thinking

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