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Job Post Details

Clinical Research Physician - job post

ICON Plc
3.4 out of 5 stars
ReadingHybrid work
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

ReadingHybrid work

Benefits

Pulled from the full job description

  • Employee assistance programme
  • Company pension

Full job description

Clinical Research Physician


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.


Clinical Research Physician - Fixed Term - one year contract

As a Clinical Research Physician at ICON, you will lead clinical trials, ensuring that they are conducted ethically and in compliance with regulatory standards.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • Leading the design and execution of clinical trial protocols, ensuring alignment with scientific and regulatory guidelines.
  • Monitoring patient safety and overseeing the clinical aspects of trials to ensure compliance with GCP standards.
  • Collaborating with cross-functional teams to analyze study data and provide medical insights that guide decision-making.
  • Engaging with investigators and study sites to ensure adherence to protocols and facilitate successful trial execution.
  • Contributing to the preparation of regulatory submissions and clinical study reports.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Medical degree (MD or equivalent) with relevant clinical research/NHS experience, essential
  • Therapeutic expertise in Respiratory and/or Transplant is desirable.
  • Strong understanding of clinical trial processes and regulatory requirements.
  • Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.
  • Effective communication and interpersonal skills, with the ability to engage with diverse stakeholders.
  • Demonstrated ability to work collaboratively in a fast-paced, team-oriented environment.
  • Willingness to travel as required (approximately 10%) - ability to attend the office 2 - 3 days a week based in Reading, Berkshire

#LI-CL1


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.

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