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Job Search Results: Jobs 1 - 10 of 185  View Titles Only  Page 1 of 19
 
Title   Company Name     Location   Date  
Job Offer in UK 

  LSC & Construction Engineer Ltd    All   28/6/2013 
Category: Engineering, Chemistry, Clerical/Administrative, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 3 years 
Area(s) of expertise desired:  
Description:
Engineers, Foremen, Captain, Mate Engineer, 2nd Engineer, 2nd/3rd Officer, Deckhand, Steward, Chef, Seafarers , Crew Job Seekers , Chief Engineer , Doctors, Nurses, Laborers, Pharmacists, Dentists, Masons, Plumbers, Drivers, Heavy equipment operators, architects, Surveyors, Customer Care Representatives.  
Requirements:
Certificates required  
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Senior Clinical Research Associate 

  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, life sciences  
Education: Bachelors   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Clinical Data Management, Clinical Research, Research  
Description:
Senior Clinical Research Associate


PURPOSE OF THE JOB

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 systems and procedures as appropriate.
Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.
Provide a benchmark for acting according to company values and act as a positive promoter


 
Requirements:
JOB FUNCTIONS/RESPONSIBILITIES

Knowledgeable of Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.
Knowledgeable of clinical 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 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.

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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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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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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Operation Deputy Manager 

  confidential    All, Rehovot   26/12/2011 
Category: Biotechnology, Engineering, Chemistry, Life Sciences,  
Education:   Position type: Full Time Team Leader  Experience:  
Area(s) of expertise desired:  
Description:
The position includes: production of company products
Maintaining and co-managing the pilot plant
Managing as well as " hand" working
the job is for Rehovot and Hedera  
Requirements:
Relevant education- Engineer/practical Engineering degree or technologist in the fields of Chemistry/food/ Biotech/engineering or first degree (Bsc) in Biotechnology
Ability for intensive and hard work and unusuall working times
wanted yet not obligated:
previous experience in producing of plant extracts; work with mechanical manufacturing devices, such as centrifuges; reactors; filtration equipment and clean room work
background and experience in food or biotechnology industry  
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manager 

  larry bee    All, chicago   15/3/2012 
Category: QA - Quality Control, IT/Hardware/Software  
Education: Masters   Position type: Full Time Manager  Experience: 6 years 
Area(s) of expertise desired: Academic  
Description:
A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.  
Requirements:
A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.  
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Clinical Study Manager 

  Hays Pharma    All   18/6/2008 
Category: Life Sciences, Clinical Research  
Education: Bachelors   Position type: Full Time Team Leader  Experience: 8 years 
Area(s) of expertise desired: Clinical Research  
Description:
Our client, a global Clinical Research Organization is seeking an experienced Clinical Study Manager to join their successful team.

Qualifications

Proven track record in study management, who possess well developed communications skills, and who will enjoy working with team. Your expertise as a Study Manager of International trials will ensure that clinical stages of research projects are completed efficiently and in accordance with customer expectations, enabling us to continue our success.

The successful candidate will have a degree, or equivalent, in a scientific or healthcare discipline complemented by solid international study management experience as a Clinical Study Manager for large scale cross-regional or International trials and previous experience as a successful and accomplished Clinical Research Associate

This role involves managing the execution of the clinical component of large, complex study protocols or global projects in accordance with the scope of work, contracted timelines and study budget. This involves the management of clinical study set-up through to the ongoing tracking and review of the study progress and reporting to relevant members of senior management.

Responsibilities

- Collaborate with other functional groups within the company such as data management, pharmacovigilance, and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
- Provide ongoing training and support to the clinical team, including the mentoring of less experienced Clinical Team Leaders. Establish study tools and training materials. Conduct frequent team meetings and ensure regular communication.
- Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team.
- Develop the risk management plan from a clinical perspective and coordinate clinical issue escalation and resolution with the Project Manager. Develop proactive contingency plans to mitigate clinical risk.
- Identify quality issues within the study through regular review of the clinical team communications including site communications, monitoring visit reports, data flow information and quality assurance audit findings. Implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
 
Requirements:
Requirements

- In depth knowledge of, and skills in applying, applicable clinical research regulatory requirements
- Bachelor's degree in a health care or other scientific discipline or educational equivalent
- significant experience working on clinical trials including monitoring as well as previous experience in a project leadership role with expanding cross-regional/global focus
 
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Mystery Shopper 

  4Service Group    All   14/5/2012 
Category: Marketing  
Education:   Position type: Part Time  Experience: No experiece 
Area(s) of expertise desired: Marketing, Sales  
Description:
4Service Group is recruiting Mystery Shoppers in israel.

As a Mystery Shopper, You will visit banks, restaurants, gas stations, retail stores, car dealerships etc., to evaluate service quality posing as a real customer. Your task is to provide an objective and timely feedback on customer service in the businesses You have chosen to visit from the available selection. Having done an evaluation, You fill in a report through 4Service web system.

We pay for each evaluation according to a fixed fee shown to You in project description before You are assigned any visits. The usual range of pay is between 10 and 20, though some assignments pay as much as 100. The payment is done via bank transfer.

Mystery Shoppers work part-time on a flexible schedule. Youll be able to choose assignments that most suit You in terms of time and location, and earn some extra income as well as help various companies improve service quality.

To get started, go to www.4service-group.com/shopper to learn more and register as a Mystery Shopper.

Should You have any questions, please send an enquiry to shoppers@4service-group.com.
ABOUT US: 4Service, established in 2001, is one the most dynamic and innovative mystery shopping agencies in Europe. As of 2012, we operate through our own mystery shopper network of 90.000 mystery shoppers in the 33 countries of Central and Eastern Europe, Balkans, Transcaucasia, Central Asia and Turkey. To learn more, please visit www.4service-group.com  
Requirements:
Between 18 and 65 y.o;
Good computer skills and stable Internet access
Honesty
Responsible and disciplined person that can be relied upon
A good eye for detail, to be able to notice important service facts
A good memory, to be able to remember important service facts
Role-playing ability flexibility, to play any evaluation scenario in a natural and easy way, just as a real customer would do
English proficiency will improve Your chances to get the best assignments
A good Mystery Shopper should take to heart the Mystery Shopping industry mission help service companies improve the service quality they deliver to their customers  
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Medical Director (9594) 

  Pharma job    All   5/5/2011 
Category: Management/Executive, Medical Management, Pharmacy/Pharmacology  
Education:   Position type: Full Time Executive  Experience: 5 years 
Area(s) of expertise desired:  
Description:
Responsibility for global medical affairs of marketed innovative product:
work with investigators, clinical associates, marketing and legal to ensure timely execution of phase IV clinical studies.
Development of global Key Opinion Leader relations.
Lead and/or support meeting and congresses, including medical congress symposia, expert meetings, advisory boards and internal meetings.
Preparation and/or review of Medical and Marketing materials.
Responses to medical questions from market.  
Requirements:
Requirements:
MD with 5-10 years of experience which includes experience in the pharmaceutical or Biotechnology Company.
Experience in a Global environment and/ or a previous similar role - a big advantage
Experience in leading clinical trials
MBA or business background - an advantage
Mother tongue level English
Excellent communication and presentation skills
Excellent analytical skills
Ability to work well in a global, complex, multi-interface structure  
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Clinical Project Manager 

  CRO    All, ISRAEL   8/8/2007 
Category: Clinical Research- Pharma-Biotech  
Education: Bachelors   Position type: Full Time Manager  Experience: 3 years 
Area(s) of expertise desired: Business Development, Clinical Research, Project Management  
Description:
To manage clinical studies
To ensure that studies are performed and completed in accordance with the pre-defined budget, timelines and quality specifications
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 GCP requirements and relevant company SOPs
Main contact with Local Regualtory Authorities.  
Requirements:
Bachelor's degree in a health care or other scientific equivalent;
Experience working on clinical trials for at least 3 years;
In depth knowledge of applicable clinical research requirements;
Strong written and verbal communication skills including good command of English language;
Computer skills including Microsoft Word, Excel and PowerPoint;
Excellent communication, organizational and problem-solving skills;
Effective mentoring, communication and training skills.  
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