Clinical Trial Associate: Research & Trial Coordination
ICON Strategic Solutions
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Benefits offered by this job
Job summary
ICON Strategic Solutions is seeking a Clinical Trial Associate to join our sponsor-dedicated team in Lund. You will assist with design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments that benefit patients worldwide.
The role emphasizes coordination, regulatory compliance, documentation, and collaboration with cross-functional teams to ensure timely, high-quality trial delivery. Travel up to 10% is expected.
Qualifications
- Bachelor's degree in a scientific or healthcare-related field.
- Experience or strong interest in clinical research.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Willingness to travel approximately 10%.
Responsibilities
- Assist in coordinating and administering clinical trials per protocols.
- Maintain and organize trial documentation, including study files, essential documents, and regulatory submissions.
- Support preparation of informed consent forms and case report forms.
- Collaborate with cross-functional teams to ensure smooth trial execution.
- Contribute to tracking and reporting of clinical trial metrics and milestones.
Skills
Education
Job description
ICON Strategic Solutions is seeking a Clinical Trial Associate to join our sponsor-dedicated team in Lund. You will assist with design and analysis of clinical trials, interpret complex medical data, and contribute to advancing treatments that benefit patients worldwide.
The role emphasizes coordination, regulatory compliance, documentation, and collaboration with cross-functional teams to ensure timely, high-quality trial delivery. Travel up to 10% is expected.
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