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PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.
PPD’s Clinical Monitoring Team is made up of monitors with institutional knowledge, in-depth therapeutic experience, and robust operational tools to help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.
The Sr. Clinical Research Associate (CRA) ensures the highest quality review of data and effective interaction with study sites. They conduct on-site monitoring visits throughout the study to help our client deliver life-changing therapies to patients. The Sr. CRA also performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures.
Responsibilities
Grow within the CRA career path to Sr CRA II or PCRA or develop into a line manager role. CRAs often transition to our client dedicated teams and to becoming CTMs working alongside our Project Management team responsible for clinical deliverables on our studies.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk - our award winning training programs speak for themselves.
To learn how PPD can advance your career, apply now!
What To Expect Next
We look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.
Qualifications
Education and Experience:
Knowledge, Skills and Abilities:
Below Is Listed The Working Environment/requirements For This Role
PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.
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