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Job Search Results: Jobs 1 - 10 of 36  View Titles Only  Page 1 of 4
 
Title   Company Name     Location   Date  
Clinical Research Physician 

  *****    Sharon Area   2/12/2011 
Category: Clinical Research, Management/Executive, Medical Management, Healthcare  
Education:   Position type: Full Time Manager  Experience: No experiece 
Area(s) of expertise desired: Academic, Internal Medicine, Oncology  
Description:


A leading international pharmaceutical company is seeking a Medical Doctor specializing in Oncology for the position of Clinical Research Physician. The CRP will manage medical domains, be responsible for the clinical studies, serve as professional authority supporting Marketing, and develop relations with opinion leaders.

 
Requirements:
An intern with sub-specialty in Oncology and experience in the Pharmaceutical Industry.

A medical graduate / Oncology specialist, experienced in the Pharmaceutical Industry will be considered too.

English fluent.

Analytic skills, presentation & communication skills.

 
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  allergy clinic    Tel Aviv Area   19/11/2008 
Category: Clinical Research  
Education: Post-Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Immunology  
Description:
 
Requirements:
 
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Application Scientist 

  Azure PCR    Jerusalem Area, Jerusalem   1/8/2013 
Category: Biotechnology, Clinical Research, Management/Executive, Sales/Marketing  
Education: Bachelors   Position type: Full Time Manager  Experience: 2 years 
Area(s) of expertise desired:  
Description:
Azure PCR develops and commercialises leading algorithm technologies for automation of molecular diagnostics data-analysis incorporating both hardware and software platforms.
For the office in Har Hatzofim an Application Scientist needed to manage the transactional process from collaborative interest/trial through to revenue. In the short to medium term, we are focused mainly on the Routine Pathogen Clinical Diagnostic market and experience in this market segment is essential.
Responsibilities include:
- Planning: development of sales strategy and an annual sales plan, and independently identifying new opportunities.
- Scientific: manage research of relevant scientific opportunities and scientific articles for peer reviewed journals
- Implementation: Turn active interest into active users, manage communication and alignment with key internal stakeholders, approach key prospects, client services to key accounts, attend and present/exhibit in key conferences, supervise external communications and the preparation of key marketing materials
- Reporting: prepare client contact and BD pipeline reports, input customer requirements to R&D/product teams to ensure development optimization, revenues (past, present and forecasts).
- Supervisory responsibilities: two members of staff Sales Support and a Graphic Designer
 
Requirements:
Education in Life Sciences, Medicine, Pharmacology or related discipline. Candidates with
relevant industry experience will also be considered (for example healthcare economics
background, etc).
At least two years experience in routine pathogen clinical diagnostics.
Graduate degree in business and/or life sciences/medicine an advantage.
Extensive relevant business development experience in the areas of healthcare licensing
and sales transactions.
Proven deal leadership skills with track record of successfully closed deals.
Experience in developing business strategies.
Fluent English
PREFERRED
Healthcare / Medical Device / Pharma / Biotech Industry experience.
Routine diagnostics testing and/or real-time PCR experience.
Published in relevant peer review journal.
Other language(s) a plus.  
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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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clinical Operations Coordinator 

  Confidential    Tel Aviv Area   4/11/2013 
Category: Clinical Research  
Education: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Academic, Clinical Data Management, Clinical Research, Other, Research  
Description:
 
Requirements:
 
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Junior Sales Representative Surgical 

  Covidien    Tel Aviv Area, Tel Aviv   27/12/2010 
Category: QA - Quality Control, Biotechnology, Engineering, Chemistry, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing  
Education: Bachelors   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: Medical Affairs, Medical Device, Sales  
Description:


Position: Junior Sales Representative Surgical (3)
Location: Central Israel (Tel Aviv)

Covidien

It's a new era with nothing but promise. Today, Covidien is more than a leading provider of medical devices, supplies and pharmaceuticals. Were a $10 billion company with over 40,000 employees who are passionate about helping doctors, nurses, and other medical industry professionals to as effective they can be.
A company with a true global mindset, Covidien has forged dynamic partnerships with medical professionals around the world. In our role as an integral collaborator, we help identify patient needs and translate them into proven procedures and products that improve and save lives.

As a Junior Sales Representative Surgical focused on our prestigious products, you will work closely with doctors, surgeons and specialist groups, selling into hospitals and a variety of practices across the centre of Israel and Central region - Jerusalem.
In return, we will provide you with world-class training, frequent development opportunities, rewarding benefits and the opportunity to work in a varied, challenging role with a large scope for demonstrating your independence, innovation and your talent for sales.

As a Junior Sales Representative your main responsibilities will involve:

Selling a portfolio of world renewed Surgical products across your established customer base
Increasing sales in line with agreed budgets
Building on well established relationships, to become an expert advisor to healthcare professionals
Being resilient, a strong negotiator and advocate for your products whilst identifying new opportunities in your market place
Cooperating with Customer Service Department
Participating in preparation and monitoring outcome of tender offers within the territory

 
Requirements:
As a Junior Sales Representative your skills and qualifications will ideally include:

Comprehensive selling experience B2B business (preferably in medical environment)
Previous sales experience or the desire to develop your sales ability
Good command of English to business standard
A full clean Driving License

What we will be looking for in you:

This role will suit a performance-driven young individual who enjoys working in a competitive environment and seizes the opportunity to get the awards that over-achievement brings. Ideally, youll have excellent presentation and negotiation skills and genuinely enjoy building long-term, trusting relationships with your customers.

Contact:

To apply follow the link:
http://www.tycohealthcarecareers.com/tycohcinternational/jobboard/NewCandidateExt.aspx?__JobID 9449

 
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Customer Relations Manager 

  Eisenberg Ventures    South Area, Rehovoth   4/5/2015 
Category: Clinical Research  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired:  
Description:
The customer relations manager will report to the CEO, handle customer accounts and provide guidance on enhancing customer relationships. Duties will include:
Be the liaison between the Company and its customers.
Work closely with the Company sales reps, distributors and service centers to (1) understand the customer environment, including customer influences, decision-makers and business challenges, and (2) support sales by orchestrating sales activities and communicating potential problems to the CEO.
Lead the implementation of a CRM system.
Creating and retaining customer loyalty and preference by establishing rapport with customers, planning and developing customer-focused programs, overseeing the resolution of customer concerns, and facilitating the delivery of goods or services to the customer.
Focus on customer service quality and product differentiation.
Assess customer needs and generate sales leads through more personalized service.
Monitor customer satisfaction and recommend approaches to better serve our customers.
 
Requirements:
At the minimum B.Sc. in life sciences (higher degree preferred). MBA an advantage
At least 2 years of experience in 3 or more of the following: product marketing, business development, marcom, B2B sales, capital equipment sales, account management, customer relations, digital marketing, distributor management.
Native English Speaker with demonstrated US business culture experience a MUST!
Self-starter with a can-do attitude a MUST!
Internet proficiency, Social Media savvy.
Team player with excellent communication skills.
Can handle multiple tasks and projects at a time, agile and responsive.
Work hours and work week are compliant to the US time zone, Monday - Friday.
 
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Manufacturing 

  Fellen Project    All   2/8/2007 
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: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Manufacturing/Production  
Description:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
Requirements:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
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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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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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