#Open_Position
#Open_positions > Study Coordinator
#Study Coordinator

Who are we looking for?

If you're a highly motivated team player, with a passion for realizing game changing medical products that can impact patients, we would love to hear from you!

We are seeking a top-notch Study Coordinator to join our Medical team and support MeMed’s clinical and medical activities. We seek a team player that enjoys working in a dynamic and creative environment. The candidate needs to be detail oriented, possess problem solving capabilities and with superb communication skills.

 

Primary Job Responsibilities

  • Responsible for ensuring study is compliance with local laws and ICH-GCP regulations.
  • Responsible for submissions to local IRB via the “matarot” system.
  • Screen potential study participants for inclusion/exclusion criteria.
  • Create and/or maintain all documents and records related to the study.
  • Entering the data into the eCRF system.
  • Manage the inventory of supplies related to the study and order more as needed.

 

Qualifications:

  • 1+ years previous experience working as a study coordinator, including involvement in IRB submissions.
  • Sc. degree in Life Science, Pharmacology, or another relevant discipline.
  • GCP/CRA Certificate.
  • Experience in database management.
  • Skilled with standard computer programs.
  • Fluent in English (oral and written).

Personal Characteristics:

  • Excellent communication and time management skills.
  • Attention to details.
  • Comfort with medical terminology.

 

Location & Scope

  • MeMed headquarters are based in Haifa, Israel. The role is for Haifa’s medical centers.
  • Full time position.