Site Monitor II - Israel - Oncology - FSP
Israel, Remote Job ID R0000029366 Category Clinical Trials Date Posted 11/12/2024Overview
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
Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do.
Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people.
Parexel FSPis looking forSite Monitor IIinIsraelto strengthen our clinical operations team. Work from home and with the flexibility you want. Our monitors have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience.
As a Site Monitor, will be responsible for data integrity, data quality and ensuring compliance with International Conference on Harmonization and Good Clinical Practice (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 the majority of activities to supplement on site visit requirements.
The Site Monitor will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready, will coordinate with institutions and investigators at the local level, and will collaborate with the Study Operations Manager (SOM), Global Study Manager (GSM), and Site Care Partner (SCP).
You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.
You will possess:
- Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.
- A minimum of 3 years' experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite).
- Minimum 3 years' experience monitoring oncology trials.
- Experience of utilizing systems like Siebel clinical trial management system (CTMS), electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF) (Florence).
- Experience in managing complex protocols in Oncology or other therapeutic areas (TA’s) where protocols are determined to be high risk.
- Proficiency in local language is required.
- English proficiency is required.
- Ability to manage required travel of up to 75% on a regular basis.
- Current driver’s license required.
Send me your updated resume tomarta.kuniewicz@parexel.comfor an immediate interview.
#LI-REMOTE
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
