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Medical Director - Remote

Posted Yesterday
All others
Full Time
USA

Overview

The Medical Director at Allucent is responsible for ensuring the medical and safety integrity of clinical trials while advising project teams and clients on safety issues.

In Short

  • Independently provide medical monitor support to clinical trials.
  • Review and analyze safety reports and clinical trial documents.
  • Prepare medical monitoring plans for trials.
  • Assist with protocol design and strategic clinical recommendations.
  • Provide 24/7 urgent medical support for safety advice.
  • Train project teams on medical aspects of trials.
  • Support business development by reviewing proposals and attending client meetings.
  • Identify trial risks and contribute to risk plans.
  • Draft and improve processes within the Quality Management System.
  • Maintain strong relationships with clients and key accounts.

Requirements

  • MD degree.
  • Minimum 5 years of relevant experience.
  • Strong knowledge of GxP and regulatory requirements.
  • Excellent communication skills in English.
  • Ability to work in a fast-paced environment.
  • Proficiency in Microsoft Office applications.
  • Client-focused and outgoing personality.
  • Administrative excellence.
  • Good standing with licensing and regulatory authorities.
  • Understanding of GDPR and HIPAA regulations.

Benefits

  • Comprehensive benefits package.
  • Competitive salaries.
  • Departmental study/training budget.
  • Flexible working hours.
  • Opportunities for remote/hybrid working.
  • Leadership and mentoring opportunities.
  • Internal growth opportunities.
  • Financially rewarding employee referral program.
Allucent logo

Allucent

Allucent™ is a dedicated partner for small to medium biopharmaceutical companies, specializing in guiding them through the complexities of clinical trials. With a focus on delivering life-changing therapies to patients globally, Allucent provides comprehensive project administration and support services to ensure projects are completed within budget and on time. The company fosters a collaborative and flexible work environment, offering opportunities for professional development and internal growth, while maintaining a commitment to quality and regulatory standards in drug development and clinical research.

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