Jobs in biotechnology, pharmaceutical, medical devices and life sciences industries.
 
Find the right job
Enter keywords
Category
Location
Position type
Jobs posted within:
 
 
 
 
 

 
Job Search Results: Jobs 1 - 10 of 183  View Titles Only  Page 1 of 19
 
Title   Company Name     Location   Date  
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.



 
To submit your resume , please sign in...
 
Senior Director of Clinical Development 

  Verna scientific    All, mountain view, CA   19/1/2007 
Category: Life Sciences  
Education: Doctorate   Position type: Full Time Employee  Experience: 5 years 
Area(s) of expertise desired: Biochemistry, Bioinformatics, Biology, Biophysics, Biostatistics, Pharmacokinetics, Pharmacology  
Description:
Responsible for all medical aspects, medical monitoring, meeting Regulatory Authority requirements, develops clinical protocols, publish, manages CRO staff, Drug Safety Service/Global Pharmacovigilance Department, Post Marketing Surveillance campaigns, interfacing with sites, vendors, investors, collaborators, customers, Regulatory Authorities and Board of Directors.

supervises biostatistical support, Clinical Program Managers (CPMs) & Clinical Research Associates (CRAs) and other clinical staff.

Acts as safety monitor for all clinical programs.

Plans and builds fully integrated Drug Safety Service (Pharmacovigilance) for products marketed or co-marketed.

Responsible for oversight of all clinical safety reports and updates to all regulatory authorities and IRBs/IECs, as well as Annual IND updates, IB revisions, protocol (safety) amendmentsl, and input to ISS (ISEs) for NDAs.
 
Requirements:
Education: MD degree is required with Minimum 5 years of experience in clinical development and all aspect of clinical trials.  
To submit your resume , please sign in...
 
Statistician - Validation/Process 

  Verna scientific    All, Swiftwater   6/6/2007 
Category: perm  
Education: Masters   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: GLP, GMP, Laboratory, Quality Control, Validation  
Description:
Responsible for providing statistical support for validation, qualification, and comparability experiments, as well as performing data analysis upon protocol execution. Will support QC in method trending and provide statistical support for laboratory investigations as needed.  
Requirements:
We are an equal opportunity employer M/F/D/V Education/Years Experience/Other Skills : MS in Statistics, Minimum 3-5 years related experience in GxP environment
Requires cGMP/cGLP training and strong writing skills along with excellent statistical, analytical and computer skills.
 
To submit your resume , please sign in...
 
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.  
To submit your resume , please sign in...
 
Statistical (SAS) Programmer 

  Verna scientific    All, Irvine   28/6/2007 
Category: Life Sciences  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Biostatistics, GLP, GMP  
Description:
Urgent requirement for one of the our top client located in 'CA.

Position Description:

This position will provide statistical programming support under the direction of the senior staff for the creation, quality control, documentation and maintenances of analysis data set, tables, listings and graphs.  
Requirements:
Requirements:

Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Science, Statistics or Statistic related field. One (1) years of pharmaceutical clinical research experience with Masters degree or Masters equivalent, or two (2) years of pharmaceutical clinical experience with a Bachelors degree or Bachelors degree equivalent.
General knowledge of medical terminology and clinical trial methodologies
Working knowledge of Base SAS, SAS/STAT; SAS Macro language a plus
Good analytical and problem solving skills
Excellent English communication skills (verbal and written) as well as good interpersonal skills
Focused, well organized, detail-oriented
Works well under pressure, with initiative to take on unfamiliar tasks.
Works well in a team environment.

Contact:

The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us to bob.harold@vernascientific.com  
To submit your resume , please sign in...
 
Gradulate students in computational and molecular biology 

  Technion    All, Haifa   13/6/2012 
Category: Life Sciences  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
Interested in addressing big questions in biology and evolution?
- How does the evolutionary process determine patterns of genetic variation?
- What is the source of the clear association between aging and cancer?
- How do bacteria adapt to changing environments and to environmental stress?
Graduate student positions are available.
- The laboratory is interdisciplinary, combining computational biology,
genomics, population genetics, microbiology and molecular biology
- Students can either do purely computational work, or combine computational
work with "wet" lab experiments
- The laboratory uses the most cutting edge genome sequencing technologies
- Work in the lab provides many opportunities for collaborations both in Israel
and abroad
- Students will have the opportunity to generate their own data and
substantiate
their results experimentally "in house" (either independently or through
collaborations with other members of the lab).

Interested? please contact me at ruthersh@tx.technion.ac.il
For more information please visit my website at:
http://hershberg.net.technion.ac.il/
(The lab is located at the Bat Galim campus of the Technion, right by the train
station and can be easily accessed from anywhere connected by train)  
Requirements:
BSc and / or MSc. in Biology, Computer Sciences, Biomedical Eng., statistics, or a related field
Strong interest in Biology
Programming skills (or a willingness to learn how to program)
 
To submit your resume , please sign in...
 
Pharmaceutical literature researcher 

  Thiolex Pharma    All   25/11/2015 
Category: Literature research  
Education: Doctorate   Position type: Temporary Employee  Experience: 1 year 
Area(s) of expertise desired: Formulation, Pharmacology  
Description:
Our company wishes to immediately engage two qualified scientists to summarize literature that is background to research that is underway in two distinct areas of development.

This relates to using methods that we will specify subsequent to your engagement. You will research and document the state of the art in internal memoranda. This will be reviewed by our patent attorneys in and disclose the prior art to our invention.

For one position, a thorough knowledge of water soluble polymers used in pharmaceutical manufacturing is required.

For the other position, a thorough knowledge of mTor in human biology and its role in various pathologies is required.

Knowledge of formulation is helpful.

At this stage, this assignment entirely involves literature search and no laboratory work.

You do not need to attend at our office to do the work.  
Requirements:
PhD is required.

Fluency in English scientific literature is required.

The core personal inventory of skills for these assignments are to:

* have a high capacity for work,
* know that you finish there will always be more to do,
* be acquisitive, curious, and innovative,
* be intellectually courageous
* demonstrate precision and discipline through your writing
* will produce work product in English

You will be engaged in an employment contract.

Either of these short-term employment positions may lead to a full time position.  
To submit your resume , please sign in...
 
Sales 

  skidoventures    All, Kuala Lumpur   17/1/2009 
Category: IT/Hardware/Software  
Education: Bachelors   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: General Services  
Description:
Responsible for assessing, planning, implementing and evaluating physical, psychological, emotional, spiritual, cultural and social needs of the resident

Validates the plan of care, goals and objectives with the resident/family  
Requirements:
Bachelor of Science Nursing or equivalent

Proven organizational, observational, interpersonal and communication skills  
To submit your resume , please sign in...
 
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.  
To submit your resume , please sign in...
 
Patient recruitment for clinical trials 

  nRollmed    All   30/4/2017 
Category: Clinical Research, Clerical/Administrative, Sales/Marketing  
Education: Associate   Position type: Part Time  Experience: No experiece 
Area(s) of expertise desired: Administration, Clinical Research, Communications, Customer Service, Marketing, Sales, Technical Services  
Description:
nRollmed - online patient recruitment & retention, is seeking for professionals to conduct phone pre-screening of potential patients considering participation in clinical trials.  
Requirements:
high marketing capabilities
ability to build trust and confidence over the phone
active listening and empathy
availability during different hours of the day
administrative capabilities
experience in clinical trials - an advantage
familiarity with ophthalmology/Optometry - an advantage.

This job is suitable for those looking for a partial position and wishing to work from home.  
To submit your resume , please sign in...
 
View saved jobs  
 View Titles Only Page 1 of 19
 
 
מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

Copyright 2005-2019 Biotech Jobs in Israel