Clinical Trial Coordinator Internship
2 settimane fa
A Clinical Trial Coordinator Intern assists the clinical research team in ensuring the conduct of studies in accordance with GCP, SOP, protocol, and budget and timelines. The role is responsible for start-up activities and document management.
Key Responsibilities- Responsible for start-up activities, including Ethic and Regulatory submission, and sites contracts negotiation under PM oversight.
- Responsible for ISF preparation and TMF setup and maintenance under PM oversight.
- Maintains relationships with ECs and CA.
- Supports sites and vendors invoicing management and tracks appropriately.
- Collaborates with weekly/monthly and ad-hoc project reports preparation and updates CTMS and study-specific trackers as needed.
- Supports CRAs activities follow-up.
- Supports document translation if required.
- Participates in internal, client/sponsor, scientific, and other meetings as required and participates in audits.
- Performs additional duties assigned.
- Graduation in a scientific/health field.
- Previous experience in clinical research in CROs, Pharma, or academia/hospital experience.
- Good knowledge of ICH GCP and appropriate regulations.
- Good knowledge of clinical research and regulatory/ethical requirements.
- English, good.
- MS Office Suite, good.
- Professional.
- Trustworthy.
- Quality-focused; ability to be careful, thorough, and detail-oriented.
- Strong organizational skills and ability to multi-task and work effectively in a fast-paced environment.
- Strong analytical skills.
- Strong communication and interpersonal skills with customer service orientation.
English
EducationBachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Pharmacy
Contract TypeApprentice (Fixed Term)
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