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**Job Title:** Clinical Research Associate
Career Description:
We are seeking an experienced and skilled Clinical Research Associate to join our team. As a CRA, you will be responsible for monitoring clinical studies to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
Key Responsibilities:
- Site Management: Verify study training records, conduct site initiation visits, and monitor data for missing or implausible information.
- Data Integrity: Safeguard data integrity through source document review, verification, query generation, and resolution.
- Compliance: Ensure sites comply with ICH GCP guidelines, applicable project plans, and Sponsor requirements.
- Collaboration: Work closely with the study team to align monitoring activities with critical study timelines.
Required Skills and Qualifications:
To succeed in this role, you must have:
- University degree or certification in a related field.
- Thorough understanding of ICH GCP guidelines and local regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently with minimal supervision.
Preferred Qualifications:
Prior experience in clinical monitoring, Phase I monitoring, or life science is highly desirable.
About the Role:
This is a challenging and rewarding opportunity to join our dynamic team and contribute to the success of our clinical trials. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply.
