- Assist in the coordination and execution of clinical trial activities under the guidance of experienced professionals.
- Maintain trial documentation and regulatory files in compliance with industry standards and regulations.
- Facilitate communication between internal team members, investigational sites, and sponsors.
- Contribute to the development and implementation of study-specific plans and procedures.
- Support data collection, entry, and quality control processes.
- Assist in organizing and preparing for investigator meetings, site initiation visits, and monitoring visits.Requirements:
- Bachelor's degree in Life Sciences or related field.
- Demonstrated knowledge of clinical trials through internships, site-level experience, or university research projects.
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to work effectively in a fast-paced environment and prioritize tasks accordingly.
- Proficiency in Microsoft Office suite.
- Prior experience in oncology clinical trials is a plus, but not required. Our client is committed to fostering a culture of learning and growth. As an Entry-Level CTA, you will have the opportunity to expand your skill set and advance your career in the field of clinical research. Join the mission to make a meaningful impact on the lives of patients battling cancer. If you are ready to take the first step towards a rewarding career in clinical research, we encourage you to apply today
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Entry level Clinical Trial Assistant - California, United States - i-Pharm Consulting
Description
As an Entry-Level CTA you will play a pivotal role in supporting our client's clinical trial operations. This is an excellent opportunity for individuals with a strong academic background and foundations knowledge in clinical trials to gain hands-on experience in a supportive and collaborative environment.
Key Responsibilities: