Clinical Scientist I
ICON plc
full-time
Posted on:
Location Type: Remote
Location: Brazil
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About the role
- Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.
- Conducting data analysis and interpretation to derive insights that support study objectives.
- Collaborating with cross-functional teams to ensure effective study execution and data quality.
- Engaging with stakeholders to communicate findings and contribute to scientific discussions.
- Assisting in the preparation of regulatory submissions, study reports, and scientific publications.
Requirements
- Advanced degree in life sciences, medicine, or a related field.
- Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.
- Excellent analytical skills and proficiency in data interpretation and statistical analysis.
- Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.
- Detail-oriented and committed to maintaining high standards of data integrity and quality.
Benefits
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Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data analysisdata interpretationstatistical analysisclinical trial protocolsregulatory submissionsstudy reportsscientific publications
Soft Skills
analytical skillscommunication skillscollaboration skillsdetail-orientedcommitment to data integrity
Certifications
advanced degree in life sciencesadvanced degree in medicine