Are you at least 3 years experienced Clinical Research Associate (CRA or Senior CRA)? Are you looking for your next step development in the Clinical Research Associate (CRA or Senior CRA) career path? Do you wish to experience innovation in your next career step as a Clinical Research Associate (CRA)?
If you are ready to make your next career step as Clinical Research Associate (CRA or Senior CRA), we are keen to speak with you today!!! Read below and apply now!
benefits
Some of the advantages you can expect from your role a Clinical Research Associate (CRA) are:
- A competitive compensation package is provided
- Consistent workload
- Career development opportunities
responsibilities
The Clinical Research Associate (CRA or Senior CRA) will perform monitoring and site management activities for Phase II-IV clinical research projects to assess the progress of clinical projects and to ensure they are conducted, recorded, and reported in accordance with the protocol, Company and Sponsor standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Primary Responsibilities
- Performing site selection, initiation, monitoring and close-out visits (on-site or remotely), according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Evaluating the quality and integrity of site practices
- Supporting the development of a patient recruitment, retention and awareness plan
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Preparation and attendance of Investigator Meetings
- Act as a primary liaison with Sponsor and study site personnel
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