Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Clinical Site Monitor I or II - FSP Oncology/Turkey
Job ID R0000022353 , RemoteParexel FSP is seeking Home-based Clinical Site Monitors/CRA I or II for
home-based positions.
Our sponsor is a global biopharmaceutical company dedicated to relentlessly seeking breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is a space where visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every decision we make and every action we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.
The Site Monitor is responsible for ensuring data integrity, data quality, and compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for most activities to supplement on-site visit requirements.
The Site Monitor will collaborate with the Site Manager to ensure that the site follows the protocol and is inspection-ready and will coordinate with institutions and investigators at the local level.
Required Experience:
A minimum of 1 year of experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite).
Site activation experience
Feasibility and site management experience.
CRO oversight experience
Submissions experience (will not be submitting as part of this role).
Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence)
Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
We offer exceptional financial rewards, training, and development opportunities. You can expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Don’t miss this opportunity. Apply today!
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