
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
November 9
🌲 North Carolina – Remote
đź’µ $131.3k - $260.7k / year
⏰ Full Time
đź”´ Lead
👨‍⚕️ Medical Director
🦅 H1B Visa Sponsor

Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
• Collaborates with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs) • Contributes medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etc • As directed supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management • Reviews and/or assists in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc,) as directed by senior management • Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc) , review of relevant therapeutic/clinical literature, and attendance in conferences and meetings • Assists in the mentoring of other medical staff as directed by Senior Management and by consistently displaying exemplary work ethics, compassion, and integrity, supports Senior Management’s leadership of both the department and the company
• Medical Degree from an accredited institution of Medical Education with a Psychiatry focus • At least 2 years of medical monitoring in a CRO • Valid passport and ability to travel as required • Excellent computer skills (Word, Excel, Access) • Excellent spoken and written English skills • Excellent organizational and time management skills • Excellent presentation skills
• Diverse and inclusive work environment • Professional development opportunities
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