Clinical Research Professional
2 weeks ago
Clinical Research Associate Role
">- This is a Clinical Research Associate position that requires strong communication and organizational skills.
- Responsible for all aspects of study site monitoring, including routine monitoring and closeout of clinical sites.
- Maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors.
About the Job
">The successful candidate will be responsible for ensuring the integrity of data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. They will also monitor data for missing or implausible data and ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to applicable regulatory requirements.
">Your Responsibilities Include:
">- Study Site Monitoring: Responsible for all aspects of study site monitoring, including routine monitoring and closeout of clinical sites.
- Maintenance of Study Files: Maintain accurate and complete records of study-related activities.
- Liaison with Vendors: Liaise with vendors to ensure timely delivery of study materials and supplies.
- Data Integrity: Ensure the integrity of data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.
- Protocol Compliance: Ensure compliance with study protocols and regulatory requirements.
Benefits
">This is a challenging and rewarding role that offers the opportunity to work in a dynamic and collaborative environment. The successful candidate will receive comprehensive training and support to ensure their success in the role.
">What We Offer
">- Opportunity to work in a dynamic and collaborative environment.
- Comprehensive training and support.
- Competitive salary and benefits package.
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