Medical Director – General Medicine

🔥 12 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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Rho

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1984

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Rho is a financial technology company that provides integrated banking solutions for businesses, combining modern banking with cash management and expense tracking. Their platform focuses on streamlining financial operations and offering a user-friendly interface for better control of company finances.

📋 Description

• Provide medical, clinical, and scientific advisory expertise across multiple therapeutic areas, including Immunology, Pain Management, Neurology, and/or Respiratory • Serve as Medical Advisor on assigned projects • Provide medical support to investigative sites and project staff for protocol-related issues • Review and clarify trial-related Adverse Events (AEs) and coding • Conduct medical case review of Serious Adverse Events (SAEs), including case documentation and patient narratives • Conduct medical review of protocols, Investigative Drug Brochures (IDBs), and/or Case Report Forms (CRFs) • Conduct medical review of Clinical Study Reports (CSRs), patient narratives, marketing applications, clinical safety/efficacy summaries and overviews, and other high-profile documents • Serve as Scientific Advisor and guide Project Managers on medical and scientific aspects of assigned projects • Participate in developing the Medical Monitoring portion of client proposals, including budgeting • Support Business Development by reviewing and providing medical/scientific input on Requests for Proposals (RFPs) • Participate as a Rho representative in bid defenses and other sponsor meetings • Support feasibility activities as required • Consult with senior management, customers, and project teams to ensure clinical-trial subject safety and the scientific and ethical integrity of trial design and conduct • Provide medical input to clinical programs and clinical development and regulatory input as needed

🎯 Requirements

• A medical degree from a fully accredited medical school • Holding (or having held) an active medical license in good standing • 5+ years of experience in clinical medicine beyond residency • 5+ years of clinical development experience, ideally in the pharmaceutical or a closely related industry • Good understanding of research methodologies and clinical trial design, including biostatistics • Good understanding of scientific and ethical regulations and guidelines pertaining to clinical research, including knowledge of federal drug development regulations and guidelines • Ability to establish and meet multiple concurrent priorities, deadlines, strategic department goals and objectives • Skills in providing consultation and advice on multiple assignments • Initiative and flexibility • Ability to establish and maintain cooperative and effective working relationships with coworkers, managers, and clients • Excellent communication and interpersonal skills, ideally with experience/expertise in public speaking and engaging external stakeholders

🏖️ Benefits

• Medical, vision, and dental insurance • Health Savings Account (HSA) • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Life and disability insurance • 401(k) • Paid time off • Holidays • Parental leave • Bereavement leave • Work-life balance and flexibility