Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.
As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.
- Full Time
- Level: Mid
- Travel: Yes
- Glassdoor Reviews and Company Rating
Success Profile
Check out the top traits we’re looking for and see if you have the right mix.
- Innovative
- Problem-Solver
- Communicator
- Tech-Savvy
- Confident
- Independent
Rewards
-
Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
-
Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
-
Collaboration
Work with industry leaders and subject matter experts.
-
Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
-
Variety
Opportunities to work on multiple accounts – never boring!
-
Compensation
Competitive salaries and bonus structure based on individual metrics.
Responsibilities
Parexel FSP is hiring for a home-based Site Monitor II and Senior CRAS.
Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionise patients’ well-being. Every choice and step we make is guided by our unwavering focus on patients, fostering an environment where innovation thrives.
The Site Monitor will be responsible for data integrity, data quality and ensuring 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.
Experience required:
• A minimum of 3 years of experience as a clinical monitor (CRA) with demonstrated experience of monitoring onsite in Turkey. A combined experience of INCRA and onsite CRA will also be considered.
• Experience in managing complex protocols in Oncology or other therapeutic areas (TAS) where protocols are determined to be high risk:
• Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
• Experience in utilising systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigational Site File (eISF) (Florence)
We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
Apply today!
#LI-TA1
#LI-REMOTE
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs