Site Monitor (CRA) II - FSP (Turkey)
Türkiye, Remote Job ID R0000033941 Category Clinical Trials Date Posted 06/10/2025Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Flexible
- Organized
- Problem-solver
- Self-starter
About This Role
Parexel FSP is currently hiring for a homebased SCRA/ Site Monitor I or II.
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 the space where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice we make and every step we take 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 assure that the site follows the protocol and is inspection ready and will coordinate with institutions and investigators at the local level.
Open to Clinical Research Associates with experience of 3 + years of independent onsite monitoring, all types of visits.
A minimum of 3 years’ experience as a clinical monitor (CRA) with demonstrated experience of monitoring onsite.
Experience in managing complex protocols in Oncology or other therapeutic areas (TA’s) 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 of utilizing systems like Siebel Clinical Trial. Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator 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!
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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
