
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
🕒 September 17
🌽 Illinois, Minnesota – Remote
💵 $97k - $193k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
• Manage research activities at sites participating in Worldwide’s clinical research projects • Participate in all stages of clinical studies, including identifying potential sites • Perform study start-up activities, collect regulatory documents, and support contract and budget negotiations • Train sites to collect data properly and report potential safety-related events • Manage site activities during study maintenance • Close down research activities at sites after study completion • Conduct study initiation visits (SIVs) • Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements
• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC Systems • 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in CNS/Neurology and/or Psychiatry required • Candidates must reside in the Central United States • Willingness to travel regionally required
• Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Regular touchpoints and coaching conversations with Line Manager • Clear career path and professional development that can lead to Clinical Trial Manager roles • Accessible Executive Leadership team • Competitive benefits package depending on location
Apply Now🕒 September 17
Clinical Trial Manager overseeing site activation, CRAs, vendors, budgets, and compliance for Linical, a clinical-trials CRO. Fully remote role supporting clinical study delivery.
🕒 September 16
Clinical scientist advancing oncology trials for Replimune’s oncolytic immunotherapy pipeline. Leading clinical documents, study execution, data analysis, and investigator collaboration.
🇺🇸 United States – Remote
💵 $159k - $205.5k / year
💰 $140M Post-IPO Equity - Replimune Group on 2024-11
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🕒 September 16
Senior Clinical Data Manager overseeing clinical trial data management from study start-up through database lock. Supporting data review, reconciliation, database testing, and regulatory-quality deliverables for BeOne Medicines.
🕒 September 15
Senior Clinical Data Manager overseeing clinical trial data operations for CTI. Managing CDM teams, data quality, budgets, deliverables, and sponsor communications from startup through archival.
🕒 September 15
Biostatistician developing analysis plans and conducting SAS analyses for Celerion’s clinical research programs. Preparing statistical reports and supporting clinical study randomization.