Senior Clinical Scientist

 Posted 2 days ago
  
 Brazil
  
⭐ 5-10 years experience
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AI Summary

The Senior Clinical Scientist leads the design and execution of clinical studies while ensuring adherence to regulatory requirements. They collaborate with cross-functional teams to analyze clinical data and provide strategic scientific guidance throughout the development process.
Senior Clinical Scientist (FSP - Sponsor Dedicated)

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 Scientist at ICON, you will design and conduct clinical studies that evaluate the safety and efficacy of innovative treatments.

What You Will Do:

Your experience in clinical research will be key in delivering high-quality outcomes and mentoring colleagues.

Key responsibilities include:

  • Leading the design and execution of clinical studies, ensuring adherence to protocol and regulatory requirements.
  • Collaborating with cross-functional teams to develop study protocols, informed consent forms, and study reports.
  • Analyzing clinical data and interpreting results to support decision-making and regulatory submissions.
  • Providing scientific input and strategic guidance throughout the clinical development process.
  • Establishing partnerships with key stakeholders to ensure alignment on study objectives and outcomes.

Your Profile:

You will have a strong foundation in clinical research, with the experience to work independently and guide others.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in clinical research and study design, preferably within the pharmaceutical or biotechnology industry.
  • Strong understanding of regulatory guidelines and requirements related to clinical trials.
  • Excellent analytical skills and experience in statistical analysis and data interpretation.
  • Strong communication, interpersonal, and leadership skills, with the ability to influence and drive results in a collaborative environment.
  • Willingness to travel as required (approximately 20%)

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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