Clinical Research Associate
2 weeks ago
We are seeking a highly skilled Clinical Research Associate to join our team at Pharmiweb. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials.
Key Responsibilities:- Site Qualification and Monitoring: Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Protocol Compliance and Data Integrity: Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Study Conduct: Collaborate with investigators and site staff to facilitate smooth study conduct.
- Data Review and Resolution: Perform data review and resolution of queries to maintain high-quality clinical data.
- Study Documentation and Reporting: Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Education: Bachelor's degree in a scientific or healthcare-related field highly preferred.
- Experience: Minimum of 2 years of experience as a Clinical Research Associate (on-site monitoring experience required).
- Skills: In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail.
At Pharmiweb, we offer a competitive salary and a range of benefits to support your well-being and work-life balance. Our benefits include various annual leave entitlements, health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme.
We are committed to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know.
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