Docs Global (Continental Europe)

Clinical Research Associate I/Clinical Research Associate II

Netanya area, Israel
28 Aug 2019
27 Sep 2019
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Job responsibilities:
•Management Clinical Trails according to the protocol and ICH GCP, standard operation procedures and monitoring plan.
•Knowledge and understanding of the protocol and CRF content
•Keeping contact with the Investigator.
•Supporting sites with all issues concerning study.
•Providing information to investigators about: protocol principles, study timelines, enrollment expectations and proposed fee.
•Preparing and performing Initiation Visit and Monitoring Visit according to the GCP and monitoring plan
•Preparing Institution and Investigator fees documentation.

What is required:
•A life science / healthcare related degree is a must
•Minimum 1-2 years of independent experience as in-house CRA or CRA
•Solid understanding of clinical trial design, trial execution and operations
.Knowledge of international standards (GCP/ICH), international (FDA, EMEA) and local regulations
•Expertise in communication, managing multiple priorities and computer literacy
•Proven people management skills with demonstrated expertise in working in a team
.•Fluency in English as well as Hebrew
•Availability to travel at least 60% fly and drive and should possess a valid driving license

What is offered:
•A challenging CRA role in an international Pharmaceutical company.
•Permanent office based position in a stable organization.
•You will enjoy highly competitive compensation and an exceptional benefits package.

Why this assigment is interesting for you:
DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.
Our people are our greatest asset.