Clinical Research Physician

ICON; Utrecht; On-site; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance options

Retirement planning

Life assurance

Flexible country-specific benefits

Job summary

ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. As a Clinical Research Physician, you will lead clinical trials, ensuring they are conducted ethically and in line with regulatory standards, with on-site availability and weekend duty as needed.

Role involves designing and executing trial protocols, monitoring safety, and collaborating with investigators and sites to drive successful outcomes.

Qualifications

• Medical degree with BIG registration is essential.
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Responsibilities

• Lead clinical trials and ensure ethical conduct and regulatory compliance.
• Collaborate with cross-functional teams to design and execute trial protocols.
• Monitor patient safety and oversee clinical aspects to comply with GCP standards.
• Engage with investigators and study sites to ensure adherence to protocols and successful trial execution.

Skills

MD/BIG registration

Clinical trial knowledge

Patient safety focus

Communication skills

Team collaboration

On-call weekends

Education

Medical degree (MD) or equivalent with BIG registration

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.

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:

Obtaining of Informed Consent

• Performing of medical assessments (such as Physical examination, evaluation of ECG e.t.c.) and evaluation of eligibility.
• 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.

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 BIG registration (essential) with relevant clinical research experience
• 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
• Availability for irregular weekend duty (on call and on site).

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What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here