Clinical Trial Lead Specialist
hace 3 días
The Senior Clinical Research Associate II (Sr CRA II) is responsible for site monitoring and site management for clinical studies according to Covance Standard Operating Procedures and Regulatory Guidelines. This includes ensuring the integrity of data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.
Key Responsibilities:
- Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
- Monitor data for missing or implausible data.
- Prepare accurate and timely trip reports.
Qualifications:
To excel in this role, you will need:
- A minimum of 3-4 years of clinical monitoring experience.
- Advanced knowledge of Serious Adverse Event (SAE) reporting and process production of reports.
- Excellent communication and interpersonal skills.
- Able to work independently and as part of a team.
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Trial Project Manager
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