Clinical Trial Coordinator Internship Specialist
7 giorni fa
Role Summary: We are seeking a highly motivated Clinical Trial Coordinator Intern to support our dynamic global team in delivering innovative solutions. As part of our team, you will be responsible for assisting in the planning, execution, and monitoring of clinical trials, ensuring adherence to Good Clinical Practice (GCP) and regulatory requirements.
Key Responsibilities:
- Assist in the preparation and submission of regulatory documents, including ethics and regulatory submissions at national and international levels.
- Support in the preparation of clinical trial protocols, informed consent forms, and case report forms.
- Collaborate with the clinical research team to ensure study conduct in accordance with GCP, SOP, protocol, and budget and timelines.
- Maintain accurate and up-to-date records, including study-specific trackers and CTMS.
- Support in the preparation of project reports, including weekly, monthly, and ad-hoc reports.
Required Qualifications and Experience: We are looking for a candidate with a graduation in a scientific or health field, previous experience in clinical research, and knowledge of ICH GCP and relevant regulations. Additionally, strong organizational, analytical, and communication skills are essential for this role.
Technical Competences and Soft Skills:
- English language proficiency.
- MS Office Suite skills.
- Professional, trustworthy, and quality-focused attitude.
- Ability to work in a fast-paced environment, manage priorities, and organize time effectively.
Education: Bachelor of Science (BS) in Life Sciences or Pharmacy.
Contract Type: Apprentice (Fixed Term).
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