Associate Medical Director

 Posted a day ago
  
 Poland
  
⭐ 2-5 years experience
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AI Summary

The Associate Medical Director provides medical expertise in the design, execution, and interpretation of oncology clinical trials. Key duties include collaborating on study protocols, providing medical oversight for safety and data, and maintaining relationships with regulatory authorities and key opinion leaders.
Associate Medical Director, Oncology

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking an Associate Medical Director to join our diverse and dynamic emerging oncology biotech team. As an Associate Medical Director at ICON, you will play a pivotal role in providing medical expertise and direction in the design, execution, and interpretation of clinical trials, contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Collaborating with cross-functional teams to design clinical development plans and study protocols.
  • Providing medical oversight and guidance throughout the lifecycle of clinical trials, including patient recruitment, safety monitoring, and data analysis.
  • Ongoing medical review of data, supporting Safety Review Committees
  • Interpreting complex medical and clinical trial data to support decision-making and regulatory submissions.
  • Contributing to the development of scientific publications, presentations, and regulatory documents.
  • Building and maintaining relationships with, investigators, key opinion leaders and regulatory authorities.

Your profile

  • Medical degree (MD) required, with board certification preferred in oncology/haematology
  • Minimum of 3 years of experience in clinical research or medical affairs within the pharmaceutical or biotechnology industry.
  • Strong understanding of clinical trial design, execution, and regulatory requirements.
  • Experience in immune oncology
  • Excellent communication and relational skills, with the ability to effectively collaborate with internal and external stakeholders.
  • Demonstrated leadership and problem-solving abilities, with a commitment to delivering high-quality results in a fast-paced environment.

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

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