Clinical Team Member

BioProtect Medical • Headquarters, KY

42d • Onsite

About The Position

Clinical Team Member
This is an ISRAELI BASED ON - SITE POSITION
Location: Netanya
BioProtect Ltd is a leading medical start up in radiation protection technology. We offer spacers protecting healthy tissue during radiation oncology treatments, based on proprietary biodegradable balloon technology.
The opportunity:
As a Clinical Team Member in BioProtect, you will be working with the clinical team, responsible for planning and execution of the company’s clinical targets.
This is an ISRAELI BASED ON - SITE POSITION
In this position you will be asked to:
Support the ongoing company clinical activities
Manage clinical data including database design, data entry and analysis
Support preparation of clinical documentation and IRB submissions as needed
Support the execution of the Post Market Clinical Follow Up (PMCF) and Post-Market Surveillance (PMS) data collection and analysis to ensure the safety and efficacy of our product.
Assist in complaint handling and vigilance activities.
Conduct literature searches and scientific articles review

Requirements

• At least bachelor’s degree in biology, Biotechnology, or related fields
• 1-3 Previous experience in clinical research with medical devices
• GCP certified
• Proficient in Excel
• High level English proficiency, speaking and writing
• A multitasker – can work with multiple deliverables, protocols and a wide range of people simultaneously. Have sense of accountability / urgency with ability to set priorities
• Proactive attitude to solving problems / proposing solutions
• Ability to work under pressure
• Excellent self-management and interpersonal skills
• Technical writing skills
• Willingness to travel abroad from time to time

Nice To Haves

• Familiar with FDA regulations
• CRA certification

Responsibilities

• Support the ongoing company clinical activities
• Manage clinical data including database design, data entry and analysis
• Support preparation of clinical documentation and IRB submissions as needed
• Support the execution of the Post Market Clinical Follow Up (PMCF) and Post-Market Surveillance (PMS) data collection and analysis to ensure the safety and efficacy of our product.
• Assist in complaint handling and vigilance activities.
• Conduct literature searches and scientific articles review

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level