Clinical Research Associate
1 month ago
About the Job
We are seeking a highly skilled Clinical Research Associate to join our team. As a key member of our site management team, you will be responsible for ensuring that clinical trials are conducted in accordance with Good Clinical Practice (GCP) and regulatory requirements.
- Prepare, conduct, and report on site selection, initiation, routine monitoring, and close-out visits to ensure compliance with GCP and regulatory requirements.
- Monitor patient enrollment to ensure recruitment targets and project timelines are met at the site and/or country level.
Responsibilities include:
Key Responsibilities
- Source data verification and follow-up on data queries at the site level.
- Review of Risk-Based Monitoring related information influencing data quality and frequency of site visits.
- Accurate and timely reporting and follow-up of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.
Requirements
To succeed in this role, you must have:
- A strong understanding of GCP and regulatory requirements.
- Excellent communication and interpersonal skills.
- The ability to work independently and as part of a team.
- Proficiency in Microsoft Office and clinical trial management software.
What We Offer
We offer a competitive salary of $80,000 - $100,000 per year, depending on experience, as well as benefits including health insurance, paid time off, and professional development opportunities.
Join Lifelancer
Lifelancer is a talent-hiring platform in Life Sciences, Pharma, and IT. Our platform connects talented individuals with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains. To apply for this position, please visit our website: https://lifelancer.com/jobs/view/80bf301b60aaff4c64323367a8bb7615
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