Clinical Trial Associate, Late Development (IIT, Registry) [GI]
| Job Title: | Clinical Trial Associate, Late Development (IIT, Registry) [GI] |
| Our Client: | A Leading Pharmaceuticals Company |
| Country: | United States |
| Location: | Jersey City, NJ (Hybrid) |
| Specialisation: | Healthcare |
| Salary: | |
| Job Reference: | 5717 |
| Contact Person: | Carson ZHU Director |
| Contact Email: | carson.zhu@cesna.com |
| Job Published: | 2025-02-14 |
Position
Clinical Trial Associate, Late Development (IIT, Registry) [GI]
About Our Client
Company provides biosimilar and innovative biopharmaceutical medications to help increase patient access to advanced therapies around the world
Job Summary
- Reporting to the Vice President Clinical Development. The Clinical Trial Associate, Late Development (IIT, Registry) [GI] will play a key role in supporting the planning, execution, and management of late phase clinical trials and responsible for providing administrative support for the trials.
- Works closely with CTM, CTL and other stakeholders
Job Description
- KEY ROLES AND RESPONSIBILITIES
- - Assist in the preparation of clinical trial documentation, including the study protocol and CSR
- - Assist clinical operation with CTM
- - Assist to provide evidence-based medical and scientific ideas for late phase trials
- - Prepare and maintain scientific literature summaries and the creation of clinical data presentations
- - Close communication with related teams in Headquarters (located in South Korea)
Qualifications
- - Minimum 1 year of experience in clinical research, clinical trials, or related fields
- - Good communication skills, both written and verbal.
- - Proactive and eager to learn about the clinical research field
- - Proactive and eager to learn about the company culture, policies, and procedures
- - Ability to work cross-functionally with various stakeholders.
- - Ability to travel across USA as needed.
- - Ability to speak both English (fluent) and Korean (Intermediate)
- - Bachelor’s degree in Life Sciences, medicine, pharmacy, or a related field.
- - Familiarity with medical terminologies, medical information reporting, and regulatory requirements.
- - Managed and maintained medical data and systems.
- - Excellent written and verbal communication skills
- - Understanding of issues in medical information and medical review
What's On Offer
Apply online or feel free to contact us directly for more information about the opportunity. Due to the high volume of applicant, we regret to inform that only shortlisted candidates will be notified. Thank you for your understanding.
Apply Now
