Job summary
Job post source
This job is directly from Parexel
Job overview
The Site and Monitoring Health Lead at Parexel oversees clinical trial monitoring effectiveness and site quality to ensure regulatory compliance and successful trial execution.
Responsibilities and impact
The role involves implementing oversight activities, reviewing monitoring reports, conducting risk-based site reviews, supporting inspection preparation, building relationships with investigators, collaborating with cross-functional teams, and leading oversight meetings.
Experience and skills
Candidates must have significant direct monitoring experience with CRO or pharmaceutical companies, lead CRA experience, knowledge of all clinical study phases, and ability to travel up to 50%. Audit and regulatory inspection experience is preferred.
Company information
Parexel is a global biopharmaceutical services company specializing in clinical research and trial management.
Team overview
The position reports to the FSP Manager and works closely with the client Associate Director and Site and Monitoring Health Team.
Job location and travel
Candidates must be located West of the Mississippi near a major airport with travel up to 50% including local, regional, and international trips.
Unique job features
The job features innovative problem-solving, risk-based monitoring approaches, and significant interaction with clinical sites and cross-functional teams.
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 extensive experience in clinical trial monitoring, particularly your knowledge of GCP regulations and risk-based oversight approaches, as these are central to the Site and Monitoring Health Lead role at Parexel.
Highlight your leadership skills in managing monitoring effectiveness, including your ability to create Study Specific Oversight Plans and conduct root cause analyses to mitigate risks at clinical sites.
Apply through multiple platforms such as Parexel’s corporate careers page, LinkedIn, and relevant clinical research job boards to maximize your application reach and visibility.
Connect on LinkedIn with professionals in Parexel’s FSP or Site and Monitoring Health teams, using ice breakers like asking about recent challenges in site monitoring or commenting on Parexel’s approach to risk-based monitoring strategies.
Optimize your resume for ATS by incorporating keywords from the job description such as 'GCP,' 'risk-based oversight,' 'clinical trial monitoring,' 'Study Specific Oversight Plans,' and 'regulatory inspection experience' to ensure it passes automated screenings.
Utilize Jennie Johnson’s Power Apply feature to automate applying across multiple platforms, tailor your resume with the right keywords, and identify LinkedIn contacts to network with, allowing you to focus your time and energy on preparing for interviews and networking effectively.
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