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
Position Summary:
The Medical Writer collaborates with members of cross-functional teams to
prepare high-quality protocols, investigator brochures, synopses, regulatory
documents, clinical publications, and related clinical documents within
agreed-upon timelines.
Essential Duties and Responsibili
The Medical Writer collaborates with members of cross-functional teams to
prepare high-quality protocols, investigator brochures, synopses, regulatory
documents, clinical publications, and related clinical documents within
agreed-upon timelines.
Essential Duties and Responsibili
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
Manages the overall planning, conduct and progress of clinical studies, and
clinical operation. The CSM carry the responsibility for making sure the
trial is planned and conducted under strict guidelines according to study
protocol and regulation and according to company needs and timelines ...
clinical operation. The CSM carry the responsibility for making sure the
trial is planned and conducted under strict guidelines according to study
protocol and regulation and according to company needs and timelines ...
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
Job Summary
The Clinical Project Manager is responsible for the routine cross-functional
operations of assigned studies.
The Clinical Project Manager is responsible for the routine cross-functional
operations of assigned studies.
לפרטים נוספים
מדעים/ביוטק
· Plans and executes clinical studies/validations and leads cross-functional
teams responsible for the planning, execution, analysis and reporting of
assigned clinical performance studies. Applies expertise in clinical data
review and statistical analysis.
teams responsible for the planning, execution, analysis and reporting of
assigned clinical performance studies. Applies expertise in clinical data
review and statistical analysis.
לפרטים נוספים
מדעים/ביוטק
A global pharma company in Rehovot is looking for a Clinical Operations
Associate, to work with local and/or global trials for all clinical phases,
in partnership with other functions.
Job description:
· Participate in the review of protocol and other study documents, manuals
and plans.
· Col
Associate, to work with local and/or global trials for all clinical phases,
in partnership with other functions.
Job description:
· Participate in the review of protocol and other study documents, manuals
and plans.
· Col
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
מדעים/ביוטק
In charge of all clinical aspects of the company
Managing FDA study and future studies
Develop a KOL network
Develop and update all clinical materials (protocols, ppt, training videos,
etc.)
Treat patients in our in-house treatment room on an ongoing basis
Clinical support to dist and users globall
Managing FDA study and future studies
Develop a KOL network
Develop and update all clinical materials (protocols, ppt, training videos,
etc.)
Treat patients in our in-house treatment room on an ongoing basis
Clinical support to dist and users globall
לפרטים נוספים