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Job Search Results: Jobs 1 - 10 of 30  View Titles Only  Page 1 of 3
 
Title   Company Name     Location   Date  
Analytical Chemist 

  Galpharma - pharmaceutical industries ltd.    Sharon Area, Or-Akiva   12/2/2008 
Category: Chemistry, Pharmacy/Pharmacology  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Analytical Chemistry, GMP, Laboratory, Quality Control  
Description:
Analytical laboratory
Galpharma - Pharmaceutical Industries ltd  
Requirements:
Knowledge and expiriene in the field of analytical chemistry and equipment  
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Chemist / A Research Management 

  halufa    North Area   7/3/2011 
Category: Chemistry  
Education: Doctorate   Position type: Full Time Team Leader  Experience: 10 years 
Area(s) of expertise desired: Analytical Chemistry, Chemical Engineering, Chemistry  
Description:
Require a leading industrial plant chemist / research manager
Education: Dr. in analytical chemistry
Masters degree in analytical chemistry with relevant experience of at least 10 years - a possible
Previous experience of between 8-10 years or more in research, analytical chemistry  
Requirements:
Proven administrative ability - Manage direct subordinates 3
Communication with external bodies
Previous experience in the field of phosphates - a significant advantage
Excellent human relations
Willingness to work hard  
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Chemistry Platform Researcher (JB-220) 

  Evogene    Tel Aviv Area   4/1/2015 
Category: Biotechnology, Chemistry  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Applied Chemistry, Biochemistry, Bioinformatics, Cheminformatics, Chemistry, Computational Chemistry, Formulation, Genetics, Project Management, Proteomics, Toxicology  
Description:
Main Responsibilities
The Chemistry Platform Researcher will Lead the design of a computational platform addressing various aspects of chemical discovery by applying innovative cheminformatics, modeling, and computational chemistry techniques.
The Researcher will work as part of a multi-disciplinary team, reporting to Evogene's Core Technologies Director.

Company Description
Evogene is a world leader in improving crop productivity and economics for the food, feed and biofuel industries. Based on a deep scientific understanding of plant genomics, a wide range of integrated computational biology capabilities and advanced breeding methodologies, Evogene offers a complete solution for crop enhancement and protection.
The growing understanding of plant genomics allows development of novel ag-chemicals with new modes of action. Recently, the introduction of ag-chemicals impacting plant growth and stress tolerance provide a major growth engine for Evogene.
Evogene was established in 2002 as a spinoff of Compugen (NASDAQ: CGEN), and employs 200 personnel, of which over 85 percent are involved in R&D. Evogene is headquartered in Rehovot, Israel. The Companys stock is listed for public trading on the Tel Aviv Stock Exchange (TASE: EVGN) and on the New York Stock Exchange (NYSE: EVGN).
 
Requirements:
Chemistry Platform Researcher (JB-220)

Main Responsibilities
The Chemistry Platform Researcher will Lead the design of a computational platform addressing various aspects of chemical discovery by applying innovative cheminformatics, modeling, and computational chemistry techniques.
The Researcher will work as part of a multi-disciplinary team, reporting to Evogene's Core Technologies Director.

Company Description
Evogene is a world leader in improving crop productivity and economics for the food, feed and biofuel industries. Based on a deep scientific understanding of plant genomics, a wide range of integrated computational biology capabilities and advanced breeding methodologies, Evogene offers a complete solution for crop enhancement and protection.
The growing understanding of plant genomics allows development of novel ag-chemicals with new modes of action. Recently, the introduction of ag-chemicals impacting plant growth and stress tolerance provide a major growth engine for Evogene.
Evogene was established in 2002 as a spinoff of Compugen (NASDAQ: CGEN), and employs 200 personnel, of which over 85 percent are involved in R&D. Evogene is headquartered in Rehovot, Israel. The Companys stock is listed for public trading on the Tel Aviv Stock Exchange (TASE: EVGN) and on the New York Stock Exchange (NYSE: EVGN).

Job Description:
The Chemistry platform will support target assessment, hit finding, and lead optimization. The Chemistry Platform Researcher will be responsible for formulating key scientific questions, translating them into computational approaches and constructing work plans for their implementation
Job Requirements:
PhD degree or postdoctoral experience in computer aided drug design, Cheminformatics or related field; first degree in Chemistry or similar;
Experience in hit-finding;
Deep understanding of the principle behind molecular recognition;
A solid understanding of quantitative data analysis, data mining
Knowledge of the principles of protein structure, function and modeling;
Excellent understanding of modern informatics methods and resources
Used to work independently and collaborate within multidisciplinary team;
Experience with one of the main modeling packages (for example, DS, Schrödinger etc.) is an advantage;
Basic programming skills - Unix / Perl / Matlab / R is an advantage

Required skills:
Must possess great interpersonal and leadership skills
Demonstrate a high level of organizational, communication and problem solving skills to address unusual situations
Demonstrated ability to innovate and work effectively in a fast-paced, complex, dynamic environment
Strong written and verbal communication skills both in in Hebrew and English
 
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Clinical Project Manager 

  Hays Pharma    All   10/7/2007 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing  
Education: Bachelors   Position type: Full Time  Experience: 4 years 
Area(s) of expertise desired: Clinical Research  
Description:
Managing all aspects of studies or study programmes allocated by the GM or SPM and to be responsible for ensuring control of allocated study budget.

 
Requirements:
Responsibilities include:

To participate in the preparation of clinical development plans
To manage clinical studies
To ensure that studies are performed and completed in accordance with the pre-defined budget, timelines and quality specifications
To participate in CRO evaluation and selection and be responsible for making selection recommendations to SPM/DGM
To coordinate the establishment of service provider contracts.
To ensure that a safety reporting system is in place and that safety reports are provided to the Safety Department in a time manner
To ensure that studies are conducted in accordance with EU GCP requirements and relevant company SOPs
To produce or co-ordinate the preparation of study protocols  
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Clinical Research Associate II 

  Hays Pharma    All   10/7/2007 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time  Experience: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Regulatory Affairs  
Description:
My client, a global leading organisation within the pharmaceutical industry, is presently seeking a Senior CRA to work over in Berkshire.

My client is looking for candidates to perform trial initiation, monitoring and close out activities in Phase II-IV clinical research, managing study site activities to ensure clinical data integrity in line with company and regulatory guidelines, and providing clinical and technical support to other CRAs and administrative staff.

As Senior CRA you will provide clinical and technical support, conduct co-monitoring/training visits and assist with protocol review, CRF and informed consent development, plus study start up activities. Where required, you will be the primary client contact for project related activities, and also act as mentor for CRAs.

 
Requirements:
Reporting to project leader, you may assume the role of a Lead CRA on projects by providing direction to the project team, coordinating monitoring activities, developing CRFs and acting as liaison between monitoring and other functions.  
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Clinical Research Associate/Senior Clinical research associate- office/home based 

  Hays Pharma    All, Izrael (anywhere)   6/11/2007 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Research  
Description:
JOB FUNCTIONS/RESPONSIBILITIES:

Recruitment of investigators.
Co-ordinate all the necessary activities required to set up and monitor a study, including the following:
Identify investigators
Help, when requested, in preparation of regulatory submissions
Design patient information sheets and consent forms.
Ensure timely submission of protocol/consent documents for ethics/IRB approval.
Placement and initiation visits.
Conduct regular monitoring visits in accordance with site monitoring SOP / Sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies.
Motivate investigators in order to achieve recruitment targets.
Complete accurate study status reports.
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
Keep the project manager informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Ensure the satisfactory close-out of investigator sites.
Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or QA personnel in the conduct of QA audits.
Maintain patient and sponsor confidentiality.

 
Requirements:
Cost effectiveness.

To participate in training new staff as appropriate.

Assist with marketing the company if and when appropriate.



QUALIFICATIONS/EXPERIENCE REQUIRED:

Medical/science background and relevant experience.

Ability and willingness to travel at least 50% of the time.(lnternational and domestic: fly and drive).

Ability to review and evaluate clinical data.

Computer literacy desirable.

Foreign language skills desirable.

Current full driving licence essential.

Good oral and written communication skills.



 
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Clinical Research Scientist 

  Makro Technologies    Worldwide   28/11/2006 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Regulatory Affairs  
Education: Bachelors   Position type: Full Time Executive  Experience: 4 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Regulatory Affairs, Research  
Description:
Full Requirement : Complete Description: Drafts protocols, formulates requirements for clinical supplies and develops CRFs.As a Clinical Research Scientist, you will participate in preparation of routine clinical documents (i.e. protocols, CRFs, GMRs, ICFs, etc.). You will prepare complex documents with moderate supervision and routine documents independently as directed by supervisor ( AHT, CAP, CDP, IND documents, etc.). You will evaluate and select potential investigative sites with minimal to moderate supervision. You will organize and present complex aspects of protocol design at investigator and internal meetings. You will also conduct initiation/monitoring visits independently, coordinate and monitor activities at clinical/investigational sites with minimal supervision by medical monitors and/or project monitors. You may also participate in training/mentoring new hires. You will oversee and coordinate the collection of and/or collect pre-study documents independently. You will monitor safety with minimal to moderate supervision via any of the following: telephone contacts, study event reports, case report form/safety report reviews, contacts with regional clinical associates (RCA), RCA monitoring trip reports, or direct site visits. You will also participate in data review and discrepancy resolution, team meetings/presentations with increasing levels of independence and may serve as Study Team Leader as well as a member of a broad range of CR&D-related and ad hoc committees as needed. You may represent organizational unit at research-wide meetings and on committees, including Global Clinical Project Teams and Interdepartmental Project Teams. In addition, you will serve as a clinical science resource for the team(s), and for peers and/or subordinates.  
Requirements:
Qualification & Skills:A BS or equivalent with a minimum of 5 years related experience or a MS degree or equivalent in Life Sciences with a minimum of 4 years related experience is required. You must have good interpersonal skills. You must have the ability to work with and negotiate with colleagues to find solutions to resource/supplies/timeline issues.  
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CRA 

  Hays Pharma    Tel Aviv Area   4/11/2008 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
Our client, a global CRO is looking for Clinical Research Associates with minimum 1 year of experience join a professional team.

The responsibility of a Clinical Research Associate II (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with companys SOPs. As Regional CRA or Primary CRA (on smaller studies) responsibilities will include managing clinical monitoring activities in addition to the ownership of investigator sites, including investigator/site selection, collating regulatory documentation, initiation and monitoring (source data verification, drug accountability and data collection) in accordance with ICH GCP guidelines.

Responsibilities

Perform clinical trial initiation, monitoring and closeout activities.
Assists with study start-up activities, site selection, and pre-study activities to identify and evaluate potential investigators.
Assists in site evaluation and reports to Lead CRA / Project Leader as appropriate.
Assists in submission of documents to the Ethics Committees, when required.
Participates in study specific training.
Assists with the preparation and coordination of investigator meetings and attends meeting.
Provide status updates of pre-study and initiation activities to Lead CRA / Project Leader.
Completes initiation visits with study staff through training, reviewing regulatory requirements, collecting outstanding documents, reviewing patient screening/randomization procedures, reviewing SAE reporting requirements, and reviewing drug storage and accountability procedures.
Assists in development of patient enrollment strategies with the project team and study site coordinator
Ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials.
Completes monitoring visits to ensure the integrity of clinical data and appropriate follow up procedures, including source document verification and SAE reporting in accordance with the project plan.
Manages study site activities and provides ongoing updates of site status to Lead CRA / Project Leader.
Maintains tracking records for assigned sites such as tracking of status and source document review per patient.
Completes study site closeout visits.
Assists with Project specific administrative activities as a member of the project team.
Ensures site registration in Investigator Database.
Increases knowledge of drug development process, therapeutic areas, Good Clinical Practices, and any applicable local regulatory requirements.

 
Requirements:


MD
Fluent official language of the country
English, written and spoken, upper intermediate
PC user
 
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CRA (Clinical Research Associate) - all levels - Israel 

  Covance    Tel Aviv Area   20/12/2017 
Category: Chemistry  
Education: Masters   Position type: Full Time  Experience: 2 years 
Area(s) of expertise desired: Clinical Research, Oncology, Research  
Description:
CRA positions available to work within our Phase II-IV Clinical
Operations Teams, Early Clinical Development or through our
CoSource division directly with pharmaceutical companies. As
an experienced CRA youll be involved in initiation, routine &
close out visits concentrating on sites in Israel. Successful
candidates will enjoy the benefits of working for a company
that values a WORK / LIFE BALANCE!  
Requirements:
As a CRA you will manage all aspects of study site monitoring
according to SOPs, GCP, and ICH guidelines, including prestudy
qualification and initiation visits, routine monitoring,
close-out of clinical sites, and maintenance of study files.
Responsibilities include:
- All aspects of site management as prescribed in the project
plans
- Recruitment of potential investigators, preparation of EC
submissions, notifications to regulatory authorities, translation
of study-related documentation, organization of meetings and
other tasks
- Negotiation of study budgets with potential investigators and
collaboration with Covance legal department with statements
of agreements
- Serious Adverse Event (SAE) reporting, production of
reports, narratives and follow up of SAEs.
- Case Report Forms (CRF) review; query generation and
resolution against established data review guidelines on
Covance or client data management systems  
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CRA II 

  Hays Pharma    All   13/7/2007 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing, IT/Hardware/Software  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research  
Description:
Our client, a worldwide Contract Research Organization, is seeking for its branch in Milan a Senior CRA to Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, SOPs/WPs, applicable regulations and the principles of ICH-GCP. Depending upon experience, become involved, when required, in other areas of study management and staff training and contribute to the review of the Company"s systems and procedures as appropriate. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues and acting according to Company"s values and as a positive promoter.

 
Requirements:
For this role is required significant experience as a CRA for at least 18 months.

This is for an international company- please provide all CV's in English format
Thankyou  
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