עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
מלאה
25,000-35,000 ₪
We are looking for an Early Clinical Study development lead who will provide essential support in the planning, execution, and management of clinical studies in the field of clinical innovation.
This role is pivotal in ensuring that our clinical trials are planned, prepared and conducted efficiently, in compliance with regulatory standards, and with the highest level of quality.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Plan and develop innovative early-phase clinical studies in collaboration with internal and external experts based on internal data and literature and under the guidance of the head of the department
Prepare essential clinical study documents
Support the submission of new studies and amendments to Ethics Committees and Competent Authorities
Schedule and coordinate meetings, teleconferences, and site visits
Assist in organizing and distributing study materials and supplies to the investigational site as needed
Facilitate communication between internal teams, CRO, and external vendors, ensuring smooth study operations
Ability to build and maintain relationships with various stakeholders
Assist in the preparation of study-related presentations, reports, and summaries for internal and external purposes
Participate in internal and external education regarding such clinical studies
Support the clinical team in various tasks as needed, contributing to the overall success of the clinical trials
This role is pivotal in ensuring that our clinical trials are planned, prepared and conducted efficiently, in compliance with regulatory standards, and with the highest level of quality.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Plan and develop innovative early-phase clinical studies in collaboration with internal and external experts based on internal data and literature and under the guidance of the head of the department
Prepare essential clinical study documents
Support the submission of new studies and amendments to Ethics Committees and Competent Authorities
Schedule and coordinate meetings, teleconferences, and site visits
Assist in organizing and distributing study materials and supplies to the investigational site as needed
Facilitate communication between internal teams, CRO, and external vendors, ensuring smooth study operations
Ability to build and maintain relationships with various stakeholders
Assist in the preparation of study-related presentations, reports, and summaries for internal and external purposes
Participate in internal and external education regarding such clinical studies
Support the clinical team in various tasks as needed, contributing to the overall success of the clinical trials
Requirements:
Qualifications:
MD or PhD in a related field (medical science, life sciences, healthcare, nursing).
CRA/GCP certificate must.
Knowledge:
Developing and writing clinical studies protocols- must.
Previous experience in pharma/biotech / medical device company must.
Previous experience as study coordinator / CRA / MSL advantage.
Excellent verbal and written communication skills in English (mother tongue level) must.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
OTHER:
Strong organizational and time management skills with the ability to handle multiple tasks and prioritize effectively.
Excellent attention to detail.
Good communication skills in Hebrew and English.
High level of integrity and commitment to maintaining confidentiality and quality standards.
Ability to work independently and as part of a collaborative team within a dynamic and fast-paced environment.
Adaptability and willingness to learn new skills and take on additional responsibilities as needed.
A positive attitude and a collaborative approach to problem-solving and teamwork.
Qualifications:
MD or PhD in a related field (medical science, life sciences, healthcare, nursing).
CRA/GCP certificate must.
Knowledge:
Developing and writing clinical studies protocols- must.
Previous experience in pharma/biotech / medical device company must.
Previous experience as study coordinator / CRA / MSL advantage.
Excellent verbal and written communication skills in English (mother tongue level) must.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
OTHER:
Strong organizational and time management skills with the ability to handle multiple tasks and prioritize effectively.
Excellent attention to detail.
Good communication skills in Hebrew and English.
High level of integrity and commitment to maintaining confidentiality and quality standards.
Ability to work independently and as part of a collaborative team within a dynamic and fast-paced environment.
Adaptability and willingness to learn new skills and take on additional responsibilities as needed.
A positive attitude and a collaborative approach to problem-solving and teamwork.
This position is open to all candidates.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
אריאל
בוקר
2 חודשים
