Job Details
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:
- 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!
Desired Skills and Experience
As an Entry-Level CTA at i-Pharm, 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 foundational knowledge in clinical trials to gain hands-on experience in a supportive and collaborative environment.
Key Responsibilities:
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.