Clinical Research Associate
hace 4 semanas
As a Clinical Research Associate at Pharmiweb, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits, ensuring regulatory, ICH-GCP, and protocol compliance.
Key Responsibilities
• Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits, ensuring regulatory, ICH-GCP, and protocol compliance.
• Evaluate overall performance of site and site staff, and provide recommendations regarding site-specific actions.
• Maintain a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes.
• Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient.
• Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site.
Requirements
• 2 years of experience as a CRA in oncology.
• Strong knowledge of ICH-GCP Guidelines, relevant regulations, and company SOPs/processes.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
About Us
Pharmiweb is a leading biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
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