
1001 - 5000 employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
đ„ 10 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
âą Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits âą Provide mentoring and guidance to less experienced CRAs and site staff when needed âą Document site visit findings via written reports âą Assess, monitor, and train study site staff on protocol adherence âą Review study subject safety information and informed consent âą Conduct source document verification for compliance, patient safety, and data veracity âą Review CRFs using paper or electronic data capture systems and assist sites with data query resolution âą Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF) âą Ensure site compliance with investigational product receipt, accountability, and return or destruction âą Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate
âą Excellent interpersonal, oral, and written communication skills in English âą Superior organizational skills with attention to detail âą Ability to work with little or no supervision âą Proficiency in Microsoft Office, CTMS, and EDC systems âą 5+ years of experience as a Clinical Research Associate âą 4-year university degree or RN/BSN in Nursing âą Willingness to travel required
âą Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law âą Diverse and inclusive work environment âą Supportive teams and accessible leadership âą Opportunities for professional growth and development
Apply Nowđ 4 days ago
Clinical Trial Manager overseeing oncology clinical trials at ICON, a global healthcare intelligence and research organisation. Managing protocols, stakeholders, compliance, vendors, risks, timelines, and budgets.
đ September 3
Clinical Trial Manager overseeing international oncology trials for Parexel, a clinical development services company. Managing vendors, CRAs, documentation, monitoring, compliance, and study execution.
đȘđž Spain â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
đ Senior
đ§Ș Clinical Research
đ September 3
Clinical Trial Manager coordinating clinical research project delivery at ICON. Leading teams, managing timelines and budgets, and ensuring quality outcomes for faster patient access to medicines.
đ September 2
EU clinical trial start-up leader managing multi-country site activation for Thermo Fisher Scientific. Leading regulatory, operational, contractual, and cross-functional delivery across European markets.
đ August 31
Senior Clinical Trial Manager executing compliant clinical studies for AbbVie, an innovative medicines company. Supporting cross-functional teams, vendors, training, protocols, and study delivery.