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Job Search Results: Jobs 1 - 10 of 27  View Titles Only  Page 1 of 3
 
Title   Company Name     Location   Date  
Extra Money in a new Sales Project 

  Con    All   23/5/2012 
Category: Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, Sales/Marketing  
Education:   Position type: Full Time Employee  Experience: No experiece 
Area(s) of expertise desired:  
Description:
International nutrition company is looking for 5 new employees to join a dynamic sales team.
Challenging job in marketing & sales.
Min 10 hrs/week.
Extra 2000-4000 nis (predictable income)
Option to work from home.
Please send CV to: project@slimail.com  
Requirements:
Please send CV to: project@slimail.com  
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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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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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Director, Clinical Operations 

  Eloxx Pharmaceuticals    Sharon Area, Rehovot   18/6/2019 
Category: Life Sciences, Clinical Research, Pharmacy/Pharmacology  
Education: Bachelors   Position type: Full Time  Experience: 10+ years 
Area(s) of expertise desired: Clinical Research, Regulatory Affairs, Start-Up  
Description:
The Role:
Reporting to the Senior Director, Clinical Operations & Site Head, the Director of Clinical Operations will be responsible for leading and managing the execution of Eloxxs clinical studies from protocol inception through study closure. This key role will manage, plan and execute clinical studies, including creating and managing study timelines, budgets and study management plans in a full out-sourced model to ensure that our corporate goals. This is a great opportunity for visibility and professional growth; the Director of Clinical Operations will manage a team of Clinical Project Managers and partner with the Senior Director to represent the Clinical Operations team cross-functionally and with key stakeholders.



Responsibilities:
Ensures that clinical trial projects are properly resourced, managed and executed within budget and in accordance with established timelines and quality standards.
Oversees the day-to-day clinical operations through a team of Project Managers with a focus on vendor management(e.g., CRO, laboratories), monitoring clinical trial recruitment rate, and coordination of activities.
Executes high quality, integrated cross-functional plans for the project/clinical trial.
Represent Clinical Operations in cross-functional teams, clinical meetings and regulatory meetings. Provide regular status updates to senior management.
Provide strategic input and drive the planning and execution for assigned clinical trials with direct responsibility for time, cost, quality, and risk mitigation.
Responsible for the oversight of protocols development; protocol preparation, amendments, CRF, informed consent form, operations and other documentation required for conduct of a clinical trial.
Accountable for internal clinical trial files and documents.
Participates and manages investigator meetings and follow up.
Travels for meetings and site visits when necessary.
Maintains proper communications with other departments to ensure good relationships in connection with ongoing set up and progress throughout trial planning and execution.
 
Requirements:
Competencies Include:
Complex problem-solving abilities with a focus on accomplishing assigned goals and objectives in a dynamic environment.
A team player who is able to effectively and flexibly lead cross functional teams across diverse cultures, backgrounds and styles.
Excellent communications and presentation skills, able to effectively inform key stakeholders and management of the status, issues and solutions.
Strong organizational and planning skills are required, with a proven ability to manage budgets and timelines.
Detail-oriented, a self-starter and comfortable with broad responsibilities in a fast-paced, small company environment.
Excellent computer skills, proficiency with project management software tools.
Prepared to travel internationally (US and EU) for approximately 7-10 days once every 2-3 months.
Flexibility to work US hours a few times a week.


Experience:
Minimum of 10 years experience in the pharmaceutical industry, with 5-7 years direct experience in planning and managing global clinical trials.
Strong people management skills with experience managing at least 2 or 3 direct reports required.
Strong bi-lingual verbal and writing skills in English and Hebrew required.
Extensive experience managing clinical programs, CROs, budgets and timelines.
Regulatory/EMA/FDA experience.
Good working knowledge of medical terminology, physiology and pharmacology and an excellent knowledge of applicable U.S. and international regulations and guidelines.
Solid understanding of pharmaceutical clinical development processes and have experience with clinical monitoring.
Ability to thrive in a fast-paced, entrepreneurial environment with busy, high performing colleagues.
Strong leadership skills and self-awareness.
Experience presenting to a varied audience, including investors and upper management.


Education:
Bachelors Degree or equivalent biologic science degree is preferred.
 
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director 

  ERICPOSEY CO LTD    Worldwide, FLUSHING   7/1/2011 
Category: QA - Quality Control, Pharmacy/Pharmacology  
Education: Masters   Position type: Full Time  Experience: 1 year 
Area(s) of expertise desired: Academic, Finance  
Description:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
Requirements:
Degree Evaluation Interviews Networking ... A less positive attribute of this job search method is that numerous ... However, the main reason why companies refrain from massively posting job details is that employers ... Community Internet Sites Many Israeli cities/regions have dedicated  
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JB-169 Computational Chemist 

  Evogene    Tel Aviv Area   4/1/2015 
Category: Biotechnology, Chemistry, Pharmacy/Pharmacology  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Academic, Applied Chemistry, Biochemistry, Bioinformatics, Cheminformatics, Chemistry, Computational Chemistry  
Description:
 
Requirements:
 
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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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Analytical Chemist 

  Galpharma - pharmaceutical industries ltd.    Sharon Area, Or-Akiva   12/2/2008 
Category: Chemistry, Pharmacy/Pharmacology  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Analytical Chemistry, GMP, Laboratory, Quality Control  
Description:
Analytical laboratory
Galpharma - Pharmaceutical Industries ltd  
Requirements:
Knowledge and expiriene in the field of analytical chemistry and equipment  
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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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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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