संयुक्त राज्य
मैरीलैंड
वर्जीनियारिमोटपूर्णकालिकजूनियरमध्य स्तरडिग्री आवश्यक नहींआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधानMonitor oncology clinical trial sites for Parexel, a provider of clinical development, regulatory, consulting, and market access services. Oversee site compliance, participant safety and recruitment, and study documentation.
Oversee investigator sites and monitor clinical trials for Parexel, supporting patient safety, GCP compliance, recruitment, and study quality. The role covers sites across the United States and is listed as remote in Arizona.
Oversee investigator sites and clinical trial monitoring for Parexel across the Central or Western United States. Support patient safety, GCP compliance, recruitment, and study quality throughout the trial lifecycle.
Support EU medicine approvals, EMA engagement, and product lifecycle strategies as a Senior Regulatory Affairs Consultant at Parexel. Lead marketing authorisation applications, regulatory dossiers, and health-authority submissions across five European countries.
Lead oncology trial monitoring across UK investigator sites for Parexel, supporting patient safety, data quality, regulatory compliance, and inspection readiness.
Parexel is hiring a Clinical Research Associate II to monitor investigator sites and support clinical trial quality, patient safety, recruitment, compliance, and close-out activities across the United States.
Support clinical trial teams at Parexel with study documentation, site payments, supplies, and Trial Master File activities in a remote Brazil-based role.
Lead clinical trial monitoring and investigator-site delivery across Turkey as a Senior Clinical Research Associate supporting Parexel’s global life sciences programs.
Lead Parexel’s enterprise data architecture strategy and modernize clinical research platforms with scalable, cloud-native systems. Drive data governance, AI innovation, and enterprise analytics to support faster clinical trials.
Lead clinical data management for Parexel’s global Phase 1–4 studies from Mexico. Oversee EDC, eCRFs, databases, vendors, and regulatory data activities while supporting cross-functional study teams.
Lead clinical data management for Parexel’s global pharmaceutical and biotechnology trials. Manage EDC systems, vendors, reconciliations, and database locks across Phase 1–4 studies.
Lead data management for Phase 1–4 clinical trials at Parexel, overseeing EDC systems, vendors, reconciliations, and database locks. Partner with cross-functional teams to maintain high-quality clinical data and study documentation.
Lead clinical data management for Parexel’s global Phase 1–4 trials, coordinating EDC systems, vendors, reconciliations, database locks, and regulatory-quality data.
Support Parexel’s clinical trial data management activities in Hyderabad, including data review, cleaning, reconciliation, and database lock preparation. Manage queries, user acceptance testing, and study documentation across Veeva Vault and eTMF.
Support Parexel’s clinical research operations and LATAM entities as a General Ledger Accountant working remotely from Argentina. Manage month-end close, reconciliations, reporting, audits, intercompany activity, and tax filings.
Senior Regulatory Affairs Associate supporting Parexel’s global regulatory compliance operations remotely in the United States. The role covers SOP governance, inspection readiness, regulatory metrics, and cross-functional compliance coordination.
