Global Clinical Trial Specialist
Insight Global
Elevate your career as a Global Clinical Trial Specialist, focusing on oncology studies and streamlining clinical trial documentation processes. This role emphasizes teamwork and the ability to manage diverse studies from start to finish. Candidates should have at least one year of clinical trial experience in the pharma or life sciences sector, with particular expertise in oncology trials. You will ensure that documentation processes adhere to ICH-GCP guidelines while collaborating with CROs and supporting submissions. Strong organizational skills are essential for managing multiple studies across various phases within deadlines. Key Responsibilities:
- Oversee clinical trials from initiation to completion
- Maintain and track essential study documentation
- Customize Expected Document Lists for each trial
- Ensure TMF documentation standards are upheld
- Support regulatory and ethics submission efforts
- Minimum 1 year of clinical trial experience
- Oncology clinical trial knowledge required
- Solid documentation experience
- Proficiency with eTMF and CTMS
- Bachelor's degree in life sciences or related fields
Vacancy posted 8 days ago
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