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Hays Pharma 
Industry Pharmaceutical
Description Hays Pharma is a leading global pharmaceutical and biotech staffing business that provides mid to upper level staff involved in drug discovery, clinical development, post-approval services and commercial activities.

Our client portfolio spans the world's leading life sciences companies in the pharmaceutical, biotechnology, generics, CRO and medical device industries. These organisations have come to depend on our professional service, innovative solutions and global reach.

With 21 offices around the world and over 350 people working through Hays Pharma and a global database of pharmaceutical professionals, we will successfully search and place over 1,000 pharmaceutical & biotech professionals this year. Hays Pharma provide the staff that help maximize returns on R&D investments and accelerate the delivery of safe and effective therapeutics to patients.
No. of Employees 51-100
Company Type Staffing firm
 
 

 
Job Search Results: Jobs 1 - 3 of 3  View Titles Only  Page 1 of 1
 
Title   Company Name     Location   Date  
Senior CRA - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Team Leader  Experience: 3 years 
Area(s) of expertise desired: Biology, Cardiology, Clinical Research, Communications, Compliance, Dermatology, Endocrinology, Executive, Gastroentology, Gynecology, Immunology, Nephrology, Neurology, Neurosciences, Oncology, Operations, Ophthalmology, Pathology, Pharmacology, Radiology, Research, Start-Up, Training, Urology, Validation, 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, 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 Company's systems and procedures as appropriate.

Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.

Provide a benchmark for acting according to our clients'values and act as a positive promoter for it.

 
Requirements:
•Knowledgeable of Company's Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

•Knowledgeable of our clients' 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 the Company's 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.

3.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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מטפלת מאגר מטפלות לילדים , אופרייות לוח דרושים הגדול בישראל כולל אלפי הצעות עבודה
 

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