Clinical Site Monitor, FSP - Oncology/Turkey
Türkiye, Remote Job ID R0000022241 Category Clinical Trials Date Posted 04/18/2024Overview
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
We are excited to announce that we are now accepting applications for our CRA Operations Talent Pipeline. We invite you to submit your basic information and resume. As soon as a suitable role becomes available, we will promptly send you an email invitation to apply officially. We appreciate your interest in our organization.
We are currently seeking Home-based Clinical Site Monitors I or II.
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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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
