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Job Search Results: Jobs 1 - 10 of 26  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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CEO is needed for a pharmaceutical company 

  Mengo    Jerusalem Area, jerusalem   23/9/2009 
Category: Biotechnology, Clinical Research, Management/Executive, Pharmacy/Pharmacology, "  
Education: MBA   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired: Executive, Oncology, "/CEO  
Description:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
Requirements:
Experience with accompanying Clinical Trials in the field drugs , preferably oncology drugs .


Experience in Business Development.


Experience from a startup company and preferably from a public company.


Experience with raising capital - as advantage.


The role includes travelling abroad.
 
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CLEAN ROOM CELL PROCESSING SPECIALIST 

  Immunovative Therapies    Jerusalem Area, Jerusalem   12/3/2013 
Category: Biotechnology, Pharmacy/Pharmacology  
Education: Bachelors   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Academic, Biology, Cell Biology, GMP, Immunology, Microbiology, Molecular Biology, Start-Up  
Description:
Company:
Immunovative Therapies, Ltd. is a biopharmaceutical start-up company headquartered in Jerusalem and Specializing in the development and production of immunotherapy drug products incorporating living Immune cells as the active ingredients.
Description:
Process patient blood and serum samples.
Work with human PBMC and maintain mammalian cell cultures.
Perform routine cell staining and flow cytometry on clinical samples.
Perform immunological-based techniques including ELISA, cytokine bead array and functional T cell assays (e.g., ELISPOT and cell proliferation).
Coordinate with team members to complete routine laboratory tasks such as reagent/supplies liquoting, restocking and ordering.
Maintain laboratory equipment and notebooks, computer files/databases.
Follow established standard laboratory operating procedures.
Hands-on lab work with long hours in a clean room environment
 
Requirements:
Requirements:
Impeccable aseptic technique skills
Ability to follow written instructions.
Knowledge of GMP manufacturing and prior experience working in a clean room.
Primary responsibility will be in cell production department.
BSc. in the biological sciences with 2+ years of related professional laboratory experience with extensive background in aseptic technique.
Experience with flow cytometry is an advantage
Experience of handling human samples and cell cultures
Highly organized, detail orientated and have strong analytical and problem solving skills
Strong record-keeping skills
Adaptable and multi-tasking
Must work well in a team environment with admirable interpersonal and communication skills in both English and Hebrew (written and oral)
Working Conditions & Physical Requirements:
This job is performed primarily in a class 10,000 clean room environment with full gowning and , working with human blood/cells in a BSC
Will require work with hazardous materials (human blood and blood components)
Requires occasional evenings and weekends work
 
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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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CRA 

  Confidential    Sharon Area   12/1/2012 
Category: Life Sciences, Clinical Research, Pharmacy/Pharmacology, Medical Equipment  
Education: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Research  
Description:
 
Requirements:
 
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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 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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director 

  ERICPOSEY CO LTD    Worldwide, FLUSHING   7/1/2011 
Category: QA - Quality Control, Pharmacy/Pharmacology  
Education: Masters   Position type: Full Time  Experience: 1 year 
Area(s) of expertise desired: Academic, Finance  
Description:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
Requirements:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
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