Clinical Research Physician
Sign up free to see how well your resume matches this role.
What you'll do
- 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.
What they're looking for
- 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).
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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).
#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.
Are you a current ICON Employee? Please click here to apply
Company
Company facts come from this company's own listings. We only show what the postings themselves carry.