מדעים/ביוטק
Job Responsibilities:
Overseeing multi-center studies in Israel, Europe, and the US.
Participate in pre-clinical and clinical study design, including selection of
study sites and vendors.
Accountable for the studies budget, quality, deliverables and timelines.
Participate in protocol developm
Overseeing multi-center studies in Israel, Europe, and the US.
Participate in pre-clinical and clinical study design, including selection of
study sites and vendors.
Accountable for the studies budget, quality, deliverables and timelines.
Participate in protocol developm
לפרטים נוספים
מדעים/ביוטק
A Clinical Research Manager is needed for the Clinical Department to assist
in all fields of ongoing clinical trials in Israel and abroad.
Role and Responsibilities
1.
in all fields of ongoing clinical trials in Israel and abroad.
Role and Responsibilities
1.
לפרטים נוספים
מדעים/ביוטק
Main Duties:
Full support to Regulatory / Clinical Strategy, including:
-Writing and reviewing regulatory documents such as SOP, CER, validations etc
-Support product regulatory submission to FDA, cFDA and EMEA
-Preparation of clinical knowledge scientific documents
-Development and execution of
Full support to Regulatory / Clinical Strategy, including:
-Writing and reviewing regulatory documents such as SOP, CER, validations etc
-Support product regulatory submission to FDA, cFDA and EMEA
-Preparation of clinical knowledge scientific documents
-Development and execution of
לפרטים נוספים
מדעים/ביוטק
The Clinical Manager will responsible for leading clinical activities related
to the development of an innovative minimally invasive surgical device. The
Clinical Manager should have a thorough understanding of all clinical
development activities and be familiar with the surgical environment.
to the development of an innovative minimally invasive surgical device. The
Clinical Manager should have a thorough understanding of all clinical
development activities and be familiar with the surgical environment.
לפרטים נוספים
מדעים/ביוטק
Primary purpose and function of this position:
o Lead, manage and coordinate clinical trials application (CTAs in EU
countries and IND in US) by close cooperation with assigned CROs and the
relevant functions inhouse , this includes:
§ Putting together the submission package in collaboration with
o Lead, manage and coordinate clinical trials application (CTAs in EU
countries and IND in US) by close cooperation with assigned CROs and the
relevant functions inhouse , this includes:
§ Putting together the submission package in collaboration with
לפרטים נוספים
מדעים/ביוטק
· Preparation of new studies (sites/CROs selection, core-documents writing,
training materials, work processes with all parties involved, submission for
study approval, sites initiations)
· Ongoing study management, including:
o Sites management / pts FU (protocol compliance, problems solving)
o C
training materials, work processes with all parties involved, submission for
study approval, sites initiations)
· Ongoing study management, including:
o Sites management / pts FU (protocol compliance, problems solving)
o C
לפרטים נוספים
מדעים/ביוטק
ROLE AND RESPONSIBILITIES
The CTM will be responsible for implementing and overseeing of clinical
trials in compliance with all applicable
county, state, and federal regulations and for ensuring the quality of the
trials.
Main responsibilities are:
· Planning and executing clinical trials with/out
The CTM will be responsible for implementing and overseeing of clinical
trials in compliance with all applicable
county, state, and federal regulations and for ensuring the quality of the
trials.
Main responsibilities are:
· Planning and executing clinical trials with/out
לפרטים נוספים
מדעים/ביוטק
Position Overview
The Clinical Regulation Specialist is responsible for ensuring that
regulatory strategies and regulatory activities are effectively executed to
meet the business objectives, regulatory and legal requirements.
The Clinical Regulation Specialist is responsible for ensuring that
regulatory strategies and regulatory activities are effectively executed to
meet the business objectives, regulatory and legal requirements.
לפרטים נוספים
מדעים/ביוטק
The Therapy Development Group Manager will lead pre- and post-market
activities for the Laser portfolio including Urology and GYN/ENT solutions.
activities for the Laser portfolio including Urology and GYN/ENT solutions.
לפרטים נוספים
מדעים/ביוטק
Medical device located in Yokneam is looking for Clinical Trial Manager (CTM)
for pre-clinical and clinical studies for full-time job.
· Conduct preparations for clinical trials (study protocols, CRF, ICF, IRB,
database building etc.)
· Conduct preparations for pre-clinical trials (study protocols
for pre-clinical and clinical studies for full-time job.
· Conduct preparations for clinical trials (study protocols, CRF, ICF, IRB,
database building etc.)
· Conduct preparations for pre-clinical trials (study protocols
לפרטים נוספים