Vice President - Medical Affairs - Endocrinology

January 16

🌲 North Carolina – Remote

Although this job is listed in North Carolina, this company may be open to hiring remote in other states.

⏰ Full Time

🔴 Lead

👔 Vice President

🦅 H1B Visa Sponsor

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Worldwide Clinical Trials

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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.

Neuroscience/Central Nervous System Clinical Research • Rare Disease Clinical Research • Oncology Clinical Research • IMID Clinical Research • Cardiovascular and Metabolic Clinical Research

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Drive development of new business via the Business Development (BD) team, including initiation/retention of relationships with current clients, potential clients, and development of new opportunities. • Participate in BD opportunities through capabilities presentation, proposal writing, bid defense participation and execution, and closing opportunities. • Build relationships with Key Opinion Leaders, therapeutic experts and clients to expand Worldwide’s portfolio. • Support existing TA-aligned operational teams, with core focus on developing comprehensive and effective strategies to maximize sales and repeat business. • Increase Worldwide Clinical Trials brand awareness by creating white papers/blogs and generating materials that showcase therapeutic and operational excellence. • Responsible for direct or indirect supervision and mentoring of all medical staff that function as Medical Monitors and medical experts, within the assigned therapeutic area. • Supervision of all medical services provided on projects with the assigned therapeutic area. • Provide support to KOL and DSMB meetings. • Support and participate in international conferences and tradeshows. • Ensures the highest level of client satisfaction through successful execution of projects. • Represents or delegates appropriate Medical Affairs functional representative to collaborate with other functions in all applicable corporate initiatives. • Implement Medical Monitoring initiatives within the company including new technology to facilitate medical oversight of projects. • Provide therapeutic training for internal and client staff, as appropriate.

🎯 Requirements

• Medical Doctor (MD) with 12 or more years of experience in clinical research and drug development. • Knowledge of all operational aspects of Phase I-IV clinical research and experience working in a pharmaceutical or biotechnology company and/or a CRO, preferred. • Demonstrated ability to establish and maintain highly effective relationships with clients, sites, key opinion leaders, and external vendors. • Detail and service oriented with the ability to work under pressure and tight timelines. • Demonstrated ability to supervise, mentor, and further develop direct reports. • Highly ethical and medically oriented.