Job summary
Job post source
This job is directly from Parexel
Job overview
The Clinical Research Associate at Parexel is responsible for ensuring data integrity, quality, and compliance with clinical trial protocols and regulations, impacting the success and compliance of clinical studies.
Responsibilities and impact
The role involves monitoring clinical trial sites virtually and onsite, ensuring regulatory and protocol compliance, verifying informed consent, reviewing source documents, managing protocol deviations, resolving data queries, and coordinating with site and study teams to meet project objectives.
Experience and skills
Candidates need at least 1 year of clinical monitoring experience, familiarity with systems like Siebel CTMS, eTMF, and eISF, and experience monitoring vaccine trials; a bachelor's degree or RN qualification is required.
Job location and travel
The position is for the Northeast or Central Region, with monitoring activities conducted mostly virtually supplemented by onsite visits.
Unique job features
The job features a hybrid monitoring approach using virtual and onsite methods, focusing on vaccine trials and utilizing specialized clinical trial management systems.
Company overview
Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services to the pharmaceutical, biotechnology, and medical device industries. They make money by offering clinical research, regulatory consulting, and market access services that help clients expedite the development and approval of new therapies. Founded in 1982, Parexel has a long history of innovation in clinical research and has been involved in the development of many significant medical treatments.
How to land this job
Tailor your resume to emphasize your clinical monitoring experience, especially your ability to ensure compliance with ICH-GCP guidelines, protocol adherence, and regulatory requirements as outlined in the job description at Parexel.
Highlight your proficiency with clinical trial management systems such as Siebel CTMS, electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF), as these are critical tools mentioned for the Clinical Research Associate role.
Apply through multiple platforms including Parexel's official corporate careers page and LinkedIn to maximize your application's visibility and chances of being noticed for the Northeast or Central Region FSP position.
Connect with current Clinical Research Associates or Study Operations personnel at Parexel on LinkedIn; initiate conversations by referencing recent vaccine trial advancements, asking about remote monitoring best practices, or expressing enthusiasm for Parexel’s approach to hybrid monitoring models as ice breakers.
Optimize your resume for ATS by incorporating keywords like 'ICH-GCP compliance,' 'clinical monitoring,' 'source document verification,' 'query resolution,' 'Siebel CTMS,' and 'vaccine trials' to ensure your resume passes automated screenings effectively.
Utilize Jennie Johnson's Power Apply feature to automate applying across multiple platforms, tailor your resume for ATS optimization, and identify relevant LinkedIn contacts for networking, allowing you to focus your energy on interview preparation and strategic follow-ups.
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