Job Title: Senior Medical Director, Medical Affairs, Endocrinology
Location: Nashville, Tennessee, United States (Remote Work Available)
Employer: Worldwide Clinical Trials - USA
Salary: Competitive
Contract Type: Permanent
Start Date: 24 February 2025
Closing Date: 26 March 2025
About the Role:
As a Senior Medical Director at Worldwide Clinical Trials, you will play a key role in providing medical oversight for endocrinology clinical trials. This involves ensuring the integrity and quality of clinical trial data, providing medical monitoring, contributing to clinical development programs, and supporting business development efforts. This role offers a unique opportunity to make a direct impact on the development of new treatments while collaborating with cross-functional teams.
Key Responsibilities:
Medical Oversight: Provide oversight for endocrinology clinical trials, serving as Medical Monitor or Global Lead Medical Monitor when applicable.
Data Review: Conduct medical data reviews to ensure accuracy, integrity, and quality.
Collaboration: Work with pharmacovigilance teams on Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
Clinical Development: Contribute to the design and execution of clinical development programs, study protocols, and research materials.
Training: Provide protocol-specific and therapeutic training to project teams.
Business Development: Support feasibility assessments, proposal generation, budget development, and sponsor engagement.
Leadership: Mentor junior medical staff, exemplifying ethics, compassion, and integrity.
Continuous Learning: Stay updated on therapeutic and regulatory advancements through conferences, literature reviews, and internal meetings.
Required Qualifications:
Experience:
5+ years of endocrinology experience.
3-6 years of medical monitoring experience, preferably within a CRO, pharmaceutical, or biotech setting.
Skills:
Strong expertise in medical data review and ensuring data quality and consistency.
Excellent organizational, communication, and presentation skills.
Proficiency in Microsoft Word, Excel, PowerPoint, and Access.
Ability to manage multiple priorities and collaborate effectively with cross-functional teams.
Travel Requirements: Ability to travel domestically up to 20%, with flexibility to provide after-hours medical support.
Why Worldwide Clinical Trials?
Worldwide Clinical Trials offers a unique environment that emphasizes collaboration, creativity, and the pursuit of excellence. As a midsize CRO, we value innovation and are committed to improving lives. Join a team where diverse backgrounds and experiences are celebrated, and where your contributions can make a meaningful difference in patients' lives.
To apply or learn more, visit Worldwide Clinical Trials' careers page or connect with us on LinkedIn.
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