
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.
🕒 July 24
🌲 North Carolina – Remote
💵 $79k - $157k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 5%
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.
• Oversee, lead, manage, and provide technical expertise within assigned projects to ensure they are executed in an efficient, accurate, and timely manner to the Sponsor’s satisfaction • Provide fully independent and autonomous leadership of data management services across multiple complex global projects/programs • Ensure appropriate resources are allocated to complete all data management (DM) activities on time and within budget • Prepare DM trial documentation, including Data Management Plans (DMPs) • Ensure effective User Acceptance Testing (UAT) is performed • Oversee data cleaning activities • Produce metrics to monitor progress of trial activities • Represent Worldwide Clinical Trials Data Management at internal and external study meeting calls • Collaborate with internal Worldwide Clinical Trials departments
• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience • Minimum of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries • Strong knowledge of data management best practices and technologies as applied to clinical trials • Strong understanding of clinical trial processes, protocol documents, and related procedures • Excellent attention to detail and strong analytical and problem-solving skills
• Competitive benefits package depending on location • Health insurance • Pay equity and transparency
Apply Now🕒 July 24
Senior CRA overseeing and managing clinical trial activities at ICON to ensure compliance with protocol and regulatory standards. Requires advanced degree and oncology monitoring experience in the Northeast region.
🕒 July 23
Clinical Trial Manager overseeing operations for clinical trials at 4D Molecular Therapeutics. Managing cross-functional team compliance and documentation for retina clinical research.
🇺🇸 United States – Remote
💵 $150k - $170k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 July 22
Senior Clinical Study Manager developing strategies for clinical research studies supporting regulatory approvals. Collaborating with stakeholders to design protocols and execute clinical studies.
🇺🇸 United States – Remote
💵 $151.7k - $218.3k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 July 22
Senior Clinical Research Scientist providing leadership in clinical study design, analysis, and evidence dissemination at iRhythm. Collaborating with cross-functional teams to drive clinical innovation and regulatory compliance.
🕒 July 22
Lead Biostatistician serving as statistical lead on pharmacovigilance projects for Thermo Fisher Scientific. Collaborating across teams to support long-term safety studies and regulatory commitments.