We are looking for an experienced Clinical Research Associate to join our client's team in Korea. The client is a biopharmaceutical company that focuses on developing and manufacturing innovative therapies for patients worldwide. As a Clinical Research Associate, you will work closely with the clinical team to ensure that clinical trials are conducted according to the protocols and regulatory requirements.
Responsibilities
As a Clinical Research Associate, your main responsibilities will include:
- Conducting site visits to ensure that the clinical trials are conducted according to the protocols and regulatory requirements
- Monitoring the progress of the clinical trials and ensuring that they are completed within the timelines and budget
- Ensuring that the trial data is accurate, complete, and verifiable by source documentation
- Coordinating with the clinical team and investigators to ensure that the trials are conducted in compliance with the protocol and regulatory requirements
- Identifying and resolving issues related to the conduct of the clinical trials
- Maintaining study files and ensuring that they are up-to-date and accurate
Skills
To be considered for this role, you should have the following skills:
- Strong knowledge of clinical research and regulatory requirements
- At least 5 years of experience as a CRA, experience in Oncology studies preferred
- Excellent communication and interpersonal skills
- Strong attention to detail and ability to work independently
- Good problem-solving skills and ability to think critically
- Ability to work in a team environment and build strong relationships with stakeholders
- Good organizational and time management skills
How to Apply
If you are interested in this position, please submit your CV to for consideration.
