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Job Search Results: Jobs 1 - 10 of 30  View Titles Only  Page 1 of 3
 
Title   Company Name     Location   Date  
147861 Field Service Engineer - USA 

  CPS    Worldwide   25/3/2008 
Category: Biotechnology, Engineering, Life Sciences, Medical Equipment, IT/Hardware/Software  
Education:   Position type: Full Time Employee  Experience:  
Area(s) of expertise desired:  
Description:
this position is a "roving" position that should be based in new jersey.
the field service engineer [fse] is responsible for the implementation of the company systems at designated medical centers. this role is the primary liaison between the medical center and the company hq for technical and training issues.
primary responsibilities:
responsible for installation, maintenance, troubleshooting and repair of optic-mechanical equipment in the field of medial devices. provide product support, software and hardware, installation, operation & servicing training to customers.
provides weekly status reports, maintains up-to-date database and field service reports.
conducts classroom, on-site and online (remote) training with the customer.
modifies, develops and maintains end-user training materials/guides.
develops and administers customer competency exams - including scoring exams, communicating results, and suggesting remedial action where needed.
facilitates system enhancement requests, system corrections, and customer issues in relevant software.
qualifications:
technical professional with expertise in a healthcare regulated environment. bachelor degree in a technical discipline, with at least 4 years practical work experience in a technical healthcare environment and medical multidisciplinary (mechanics, optics, electronics, software, etc.) devices.
demonstrated success in working with customers (mainly hospitals), vendors, and leading cross-functional teams. interpersonal skills and customer service orientation.
strong process orientation, problem solving & troubleshooting skills, and a firm commitment to quality operating with various computer software.

excellent presentation, communication and conflict management skills.
knowledgeable in the system design, build, testing, training, supporting and go-live activities.
willingness to travel up to 80%, including overnight stays with trips to the company headquarters in israel.
displays professional, team-oriented attitude to co-workers and customers.
ethics and integrity - strong interpersonal with a high degree of self-motivation and ability to work independently away from the headquarters, peers and managers. responsible, independent and accurate.
excellent verbal communication skills.

a calm, helpful demeanor and the ability to handle deadlines and cope with stressful situations.  
Requirements:
 
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Business Development Manager 

  Biopharmax    Tel Aviv Area   19/6/2012 
Category: Management/Executive, Medical Equipment, Sales/Marketing  
Education:   Position type: Full Time Executive  Experience:  
Area(s) of expertise desired:  
Description:
A growing company in the Medical Devices Industry is looking for a Business Development Manager to build and develop the business throughout the world (Out of US).
Work includes analyzing and understanding of the markets in each country, searching for the proper distribution channels, closing new agreements and maintaining current ones.  
Requirements:
Experience in Medical devices industry and in opening of new distribution channels
Availability and willingness to frequent travels abroad
High level English, additional languages - advantage
Living in the north (company is located at Tefen)
there is possible to work from the center(Herzeliya Pituach)

Company Website www.equashield.com  
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Clinical Application Development Scientist (position # 1296) o 

  Mengo    North Area, Yokneam   14/5/2010 
Category: Clinical Research, Medical Equipment  
Education:   Position type: Full Time  Experience: 4 years 
Area(s) of expertise desired: Clinical Research, Surgery  
Description:
Please send your resume in a .doc format to jobs2@mengo.co.il
You must indicate at the headline of your email the no. of the position 1296

Affiliation: reporting to the Medical Director

Job Description and Main Tasks:
Acquisition, analysis and reporting of application related technological, scientific and clinical data including and maintenance of a clinical and scientific database (scientific literature, internet, market reports, etc.).
Professional support of the Medical Director activities including: writing protocols, multi-centers studies, coordination with physicians, laboratories and hospitals, issuing reports, etc.
Writing reports for in-house and external purposes and preparing multimedia presentations.
Assisting in writing scientific papers.
Working closely with bodies within and outside the company including CROs, clinical monitors, MDs nurses, etc.
Active participation in the R&D Application Group activities.
 
Requirements:

Qualifications:
Academic M.Sc. or preferred Ph.D. in either: bio-medical engineering, medical science, biology, medicine (MD) or equivalent.
At least 5 year experience in a medical device company.
Mother tongue level English.
Ability to read and analyze high volumes of scientific data.
Journal level scientific papers writing capability.
Familiarity with operating rooms environment and equipment and with surgical procedures.
Familiarity with regulatory processes (FDA, CE, IRB) - advantage.
Reliability, team worker, excellent inter-personal relationships.


 
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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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Development Lead 

  Vensica Medical    Tel Aviv Area, Givataim   16/8/2015 
Category: Engineering, Medical Equipment  
Education:   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Engineering, Start-Up  
Description:
Vensica Medical is a start-up developing a Revolutionary Needle-Free Way To Effectively Deliver Drugs To The Urinary Bladder based on therapeutic ultrasound.

We are looking for a talented and experienced engineer to lead the product development.

The position entails:

Product design and lead
Lab and para-clinical trials management
Model building
Managing sub-contractors
 
Requirements:
Mechanical / Bio-medical / Physics Engineer
At least 3 years of experience managing product development in a bio-medical company
Experience in project lead and lab management
Para-clinical trial experience
Familiar with development protocols, QA and POCs
Independent and Motivated  
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