On-site CRA II, Israel
- Employer
- Syneos Health
- Location
- Israel (IL)
- Salary
- competitive
- Start date
- 19 Apr 2019
- Closing date
- 19 May 2019
View more
- Discipline
- Clinical Research, Study Site Coordinator
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Clinical Research Associate I/II
Israel, office-based
Permanent contract
Sponsor-dedicated
Summary:
Here at Syneos Health we are currently recruiting for an experienced Clinical Research Associate II to be based in office in Israel and work closely with one of Global Pharmaceutical company client. The role does not require travel.
Responsibilities will include:
-
eCRF data entry of trials specific data
-
Responding to data queries raised from Sponsor/CRO
-
Liaise support Sponsor CRO visits ensuring data is accurate and available
-
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements.
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Responsible for completion of all study documentation forms, including case report forms and other study specific documents.
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Development of patient source note templates.
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Investigator site file maintenance.
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Support Trial invoicing to CRO with verification of patient visit schedules
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Perform quality control on study documents and maintain an up to date master schedule of study activities, whilst assisting with data management. You will also maintain up to date study files and ensure all relevant documentation is present.
-
Help organize site layout to facilitate accurate data collection, recordkeeping and regulatory documentation
The ideal candidate will need the following experience / skills to be considered:
- Minimum of 1-2 years of clinical monitoring.
- Start-up experience will be asset.
- Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
- Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
- Good written and verbal communication skills. Written and verbal fluency in English and Hebrew.
- Previous experience with electronic data capture systems is desirable.
We have a comprehensive benefits package and offer highly competitive remuneration.
If you have the required experience for this position and are eligible to work in the required location then please apply by CV.
Please be advised that due to volume of received applications, only selected candidates will be contacted back.
To find out more about our company and search and apply for other open jobs please visit our website https://www.syneoshealth.com/
Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
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