Medasense Published: April 24, 2019
Job Type
Level of education
Vocational qualification
Spoken Language needed
English
Level of Hebrew
Medium
Location of job
Tel Aviv/ Ramat Gan
How many relevant years experience do you require for the role:
1 year

Description

The CRC (Clinical Research Coordinator) will be responsible for the implementation of the research together with hospital and research staff to ensure successful completion of study goals.

Duties and Responsibilities
- Assists in the recruitment of study subjects and provides instructions to meet the goals of the study.
- Collects data from study subjects and enters information into the designated case report forms/database to comply with study protocols. Part of the data collection is to be recorded during surgeries in OR room.
- Identifies and reports issues that may affect the accuracy and quality of study design and implementation to meet study aims.
- Ensure the filing and maintenance of all regulatory documents
- Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival
- Other duties as assigned.
- Adhere to Good Clinical Practices and the study protocols
- The first 8 months requires working full time on a project at Shaare Tsedek Hospital, Jerusalem

Requirements

- Bachelor’s degree in a health or science related field (Nurse Certificate)
- GCP and CRA certification
- Experience with clinical trials
- Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals.
- Proficiency in English and Hebrew
- Medical Skills: Comfort with attending surgeries/OR presence.
- Medical device industry – Advantage
- Patient monitoring and anesthesia background - Advantage
- Must be very accurate with high attention for details
- Self-managed and highly organized
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