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Clinical Trial Manager

Key Facts

Remote From: 
Full time
Mid-level (2-5 years)
English

Other Skills

  • •
    Communication
  • •
    Team Leadership
  • •
    Relationship Building
  • •
    Time Management
  • •
    Collaboration
  • •
    Personal Integrity

Roles & Responsibilities

  • Strong experience in a Senior CRA or CTM position at a CRO or Pharmaceutical Organization
  • Bachelor's degree in health, life sciences, or other relevant fields
  • Preferred: 2+ years of monitoring experience
  • Ability to manage multiple vendors and stakeholders

Requirements:

  • Budget oversight of the clinical portion of the budget to ensure efficient resource allocation
  • Develop monitoring plans and tools to ensure effective study oversight
  • Train and mentor Clinical Research Associates (CRAs) to optimize their performance
  • Drive enrollment and lead study start-up activities, adhering to timelines

Job description

Clinical Trial Manager (CTM) - Brazil - Homebased

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.


As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs

What You Will Do:

Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.

Key responsibilities include:

  • Budget Oversight the clinical portion of the budget to ensure efficient resource allocation.

  • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.

  • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.

  • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.

  • Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.

  • Building Productive Relationships: Foster productive relationships with Sponsor, vendors, and cross-functional teams.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Strong experience in a Senior CRA or CTM position at a CRO or Pharmaceutical Organization.

  • Bachelor's degree in health, life sciences, or other relevant fields of study.

  • Preferred: 2+ years of monitoring experience.

  • Ability to manage multiple vendors and stakeholders

  • Contribution to the implementation and optimization of hubs

  • Risk management

  • Data-driven decision making (DDM)

  • Ability to manage a high workload with multiple priorities

  • Use of digital tools (eConsent) and AI implementation

  • Strong Communication and Site Engagement Skills

#LI-AR1

#LI-Remote


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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