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Job Search Results: Jobs 1 - 10 of 182  View Titles Only  Page 1 of 19
 
Title   Company Name     Location   Date  
Senior Clinical Research Associate - homebased 

  CRO PharmaNet Services GmbH    All, Israel (home-based)   10/6/2008 
Category: Clinical Rsearch  
Education: Bachelors   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Regulatory Affairs  
Description:
The role will involve
• Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance
• Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines
• Recruit investigators
• Negotiate study budgets with investigators
• Obtain, review, and process regulatory and administrative documents from investigator sites
• Review and develop protocols
• Review and develop CRFs
• Coordinate and present at Investigators’ Meetings
• Participate in proposal meetings with potential clients
• Prepare and review Serious Adverse Event (SAE) reports
• Prepare project management reports for clients, project personnel, and PharmaNet management
• Resolve issues, questions, and requests for additional study supplies
• Review and approve monitoring trip reports
• Review and verify completed CRFs
• Review clinical data in-house
• Resolve queries of CRF data with study site personnel
• Review Tables and Listings generated from study data
• Author Clinical Study Reports
• Train and mentor CRAs on monitoring, internal procedures, and query resolution
 
Requirements:
The ideal candidate will have
• Bachelor’s Degree or nursing credential
• Three and a half years’ experience in clinical research, data management, or regulatory affairs
• Twenty four months’ field monitoring or equivalent experience
• Ability and willingness to travel 50% of the time
• Excellent organizational skills
• Ability to manage time and work independently
• Excellent written and oral communication skills
• Fluent in English and Hebrew

If you think you’ve got the necessary skills and experience, please send your CV electronically in English to Andrea Kunz (Recruiter Europe): akunz@pharmanet.com
or call for additional information at +49 6102 813 204
or visit us at www.pharmanet.com.
Please include you availability and your salary expectations.

 
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CRA - International Company - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired: Biology, Cardiology, Chemistry, Clinical Research, Endocrinology, Gastroentology, Gynecology, Immunology, Infectious Disease, Internal Medicine, Nephrology, Neurology, Oncology, Ophthalmology, Pharmacology, Urology, Virology  
Description:
Identify, select, initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with our client's SOPs/WPs, applicable regulations and the principles of ICH -GCP.  
Requirements:
Familiarity with Companys' Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

Familiarity with Company's Systems

Familiarity with principles of investigator recruitment.

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.
Coordinate documents translation, verification and back translations where required.
Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements.
Pre-study and initiation visits.
Conduct regular monitoring visits in accordance with our client's site monitoring SOP/Sponsor site monitoring SOP/WP, 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 regularly 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.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or Company's QA personnel in the conduct of QA audits.
Participate in feasibility studies for new proposals, as required
Maintain patient and sponsor confidentiality.
To be cost effective
To participate in mentoring of new staff up to Clinical Research Associate level 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 (international 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.

HAYS Pharma provides extensive resourcing solutions to the pharmaceutical industry. Having established relationships with the world`s leading organisations within Pharmaceutical / Biotech / Clinical Research / Consulting industries our consultants are ideally placed to provide our candidates with their next best career opportunity.

Services advertised by Hays Pharma are those on an Agency and/or an Employment Business.



 
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CRA II - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Biology, Cardiology, Clinical Research, Communications, Compliance, Dermatology, Endocrinology, Gastroentology, Gynecology, Immunology, Infectious Disease, Nephrology, Neurology, Oncology, Operations, Ophthalmology, Pharmacology, Radiology, Urology, Virology  
Description:
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 and in accordance with Company's SOPs/WPs applicable regulations and the principles of ICH-GCP.

Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.
 
Requirements:
Knowledge of Company's Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

Knowledge of Company's systems

Recruitment of investigators.

Independent and proactive coordination of all the necessary activities required to set up and monitor a study, including but not limited to the following:
Identify investigators.
Help when requested, in preparation of regulatory submissions.
Design of patient information sheets and consent forms.
Coordinate documents translation, verification and back translations where required.
Ensure timely submission of protocol/consent/Safety reports documents for ethics/IRB approval.
Pre-study and initiation visits.
Conduct regular monitoring visits in accordance with our client's site monitoring SOP/Sponsor site monitoring SOP/WP, 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 regularly informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Participate in feasibility studies for new proposals, as required
Ensure the satisfactory close-out of investigator sites.
Act in a Lead role on a study, assuming additional responsibilities as detailed/documented by the Clinical Project Manager (CPM), if appropriate.
Ensure correct archiving of files on completion of a study.
Maintain patient and sponsor confidentiality.
Assume additional responsibilities as directed by Associate Clinical Project Manager/CPM/Clinical Project Director.

To be cost effective.

Participate in mentoring new staff.

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 (international 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.

HAYS Pharma provides extensive resourcing solutions to the pharmaceutical industry. Having established relationships with the world`s leading organisations within Pharmaceutical / Biotech / Clinical Research / Consulting industries our consultants are ideally placed to provide our candidates with their next best career opportunity.

Services advertised by Hays Pharma are those on an Agency and/or an Employment Business.

 
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Senior CRA - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Team Leader  Experience: 3 years 
Area(s) of expertise desired: Biology, Cardiology, Clinical Research, Communications, Compliance, Dermatology, Endocrinology, Executive, Gastroentology, Gynecology, Immunology, Nephrology, Neurology, Neurosciences, Oncology, Operations, Ophthalmology, Pathology, Pharmacology, Radiology, Research, Start-Up, Training, Urology, Validation, Virology  
Description:
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 Company's systems and procedures as appropriate.

Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.

Provide a benchmark for acting according to our clients'values and act as a positive promoter for it.

 
Requirements:
•Knowledgeable of Company's Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

•Knowledgeable of our clients' systems

•Recruitment of investigators.

•Independent and proactive co-ordination of 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.
-Co-ordinate documents translation, verification and back translations where required.
-Ensure timely submission of protocol/consent documents/safety reports for ethics/IRB approval according to local requirements.
-Placement and initiation visits.
-Conduct regular monitoring visits in accordance with the Company's 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 regularly 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.
-Maintain patient and sponsor confidentiality.
-Assume additional responsibilities as directed by Associate Clinical Project Manager/Clinical Project Manager (CPM).
-Responsible for the conduct/management of any aspect(s) of a project, when requested and authorised by a CPM/Associate Clinical Project Manager.
-Co-ordinate and/or participate in feasibility studies for new proposals, as required.

•Be cost effective.
•Participate in mentoring and training new staff.
•Assist with marketing the company if and when appropriate.

3.QUALIFICATIONS/EXPERIENCE REQUIRED:

•Medical/science background and relevant experience.

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

•Ability to review and evaluate clinical data arising from aptitude and have the required level of experience in Clinical Research.

•Computer literacy required.

•Foreign language skills desirable.

•Current full driving licence essential.

•Good oral and written communication skills.
 
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Computerized systems validation engineer 

  Comply    All   1/4/2015 
Category: QA - Quality Control, IT/Hardware/Software  
Education: Bachelors   Position type: Full Time  Experience: No experiece 
Area(s) of expertise desired: Business Analyst, Compliance, GLP, GMP, Information Systems, Medical Device, Other, Professional Services, Validation  
Description:
•Write Computerized systems validation documents and test protocols: STP,STD,IQ,OQ,PQ
•Write Computerized systems design and summary documents: URS,FRS,VP,STR,VSR
•Write SOPs ( Standard Operating Procedures) , Work instructions
•Write software applications reject lists, bug identification, report and monitoring.
•Functional testing of life-science computerized systems.
 
Requirements:
Minimum Qualifications

•Education: BA/BSC in Biotechnology, Chemical Engineering, Biomedical engineering, Chemistry, Biology, Computer Science
•Communication: Excellent oral and exceptional technical writing skills with the ability to interface effectively and professionally at all levels.
•Organized person with high ability to work with fine details.
•Excellent English( Equal to mother tongue).
•QA oriented : Experience with QA in the life-science industry( Pharma ,Biotech and Medical devices). Optional- Experience with QC in the life science industry.
•Service oriented.

Preferred Qualifications

•Experience with use of life science computerized system ( e.g. LIMS, ERP systems, computerized Lab systems ( Empower, FTIR etc..), production systems etc.)
•Experience with IT subjects (i.e. Server- Client topology, Data backups, Help Desk etc.)
•Experience in software testing\ computerized system validation in the life science industry
•Knowledge in roles and guidelines: 21CFRPart11, GAMP5 ISO 14971:2007,IEC 62304
 
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Work in Singapore 

  TWLink Technologies Pte Ltd    All   13/9/2007 
Category: job posting  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Cardiology, Career Planning/Placement, Genetics, Oncology, Pharmacology  
Description:
All the expertise areas listed below.  
Requirements:
Able to work in Singapore  
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management 

  MECO IND    All, new york   15/10/2007 
Category: Chemistry  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired: Administration  
Description:
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Requirements:
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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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Researcher 

  Immunovative Therapies Ltd.    All, Jerusalem   1/1/2008 
Category: Life Sciences  
Education: Masters   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired: Cell Biology, Cell Culture, Molecular Biology  
Description:
Immunovative Therapies, Ltd. is an early stage biopharmaceutical company specializing in the development of immune cell-based therapies for cancer and infectious diseases. We are seeking a Research Associate in Jerusalem to join our team.  
Requirements:
Master’s degree in cell and/or molecular biology and at least 2 years academic or industrial lab bench experience; knowledge of and experience with cell culture procedures - subculture, cryopreservation, cell counts, and staining; knowledge of biochemical and molecular biology procedures and methods, especially nucleic acids extraction, reverse transcription, quantitative polymerase chain reaction; experience with ELISA and ELISPOT assays. Knowledge of immunology helpful. Must be fluent in English.

 
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CLINICAL RESEARCH ASSOCIATES (all levels) 

  Hays Pharma    All   30/9/2008 
Category: Clinical Research  
Education:   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired:  
Description:
Our client, a highly reputable leading global Contract Research Organisation, is looking for Clinical Research Associates to join the team. The purpose of the role is to identify, select, initiate and close-out appropriate investigational sites for clinical studies and to monitor these sites ensuring that the studies are performed in accordance with the SOPs, applicable regulations and ICH-GCP guidelines.

ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.

 
Requirements:
Education and qualifications

Medical/science background and 1 year previous clinical research experience;

Ability and willingness to travel at least 50% of the time;

Ability to review and evaluate clinical data;

Computer literacy desirable;

Good use of English;

Good oral and written communication skills.


 
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