Job Search Results: Jobs 1 - 10 of 63  View Titles Only  Page 1 of 7   Title   Company Name     Location   Date   עובד מעבדת מחקר    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: To submit your resume , please sign in...   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 company’s 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   To submit your resume , please sign in...   Medical Advisor-Greece    Hays Pharma    Worldwide   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: Medical Advisor opportunity has arisen within a blue-chip pharmaceutical company in Athens. This is a highly interactive role, demanding effective strategic thinking and planning skills and the ability to network, teamwork and build influential relationships with your colleagues, customers and external opinion formers. As a Medical Advisor you will provide a specialist role in a number of therapeutic areas. You will work closely with your commercial colleagues to provide pro active input into the strategic management of the business, jointly agreeing, developing and implementing strategic direction within key therapeutic areas, allowing commercial aims and ambitions to be met. The role requires a good understanding of clinical development processes and of the changing health care environment Accountabilities Providing authoritative opinion on medical, legal and regulatory matters to support your colleagues across the UK, enabling them to comply with the relevant statutory requirements (e.g. Code of Practice, Medicines Act, and EU Directives). Provision of pro active input to the development of business strategy. Effectively developing relationships with key influencers and external organizations to ensure that the company retains a leading voice in the pharmaceutical industry. Coordinating and utilizing specialist knowledge with brand aligned colleagues in formulating and implementing short and long term medical strategy for optimal commercial benefit. Working closely with regulatory, commercial and clinical colleagues on pre-launch planning, including strategic evidence planning and generation. Influencing clinical research strategies in support of market needs Provide medical information Knowledge of the clinical practice, care pathways, key competitors, etc. and input where required into study allocation process. Input into a development of local protocols, patient information customer-initiated research projects (CIRPs) and named patient programmes. Input into reviews and sign off of abstracts, reports and publications. Pro active input into European Medical meetings to ensure strategy is supported. Review and sign-off Regulatory documents as required.   Requirements: Qualifications/Experiences A registered medical doctor. Expert therapy knowledge in a broad range of therapeutic areas, Continuous record of career achievement through clinical development and/or medical affairs positions. Previous industry experience would be beneficial A good understanding of the changing health care environment.   To submit your resume , please sign in...   CLINICAL TEAM LEAD    Hays Pharma    All   30/9/2008  Category: Clinical Research   Education:   Position type: Full Time Employee  Experience: 3 years  Area(s) of expertise desired: Clinical Research   Description: An excellent opportunity has arisen to join this global Contract Research Organisation as a Clinical Team Lead. The purpose of the role is to manage the execution of the clinical component of study protocols in accordance with the scope of work and contracted timelines. May act as a CTL for large scale projects under the supervision of a more senior CU, or Line Manager. May also serve as a Sr Clinical Research Associate (Sr CRA) within the project or other projects as needed. ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.   Requirements: REQUIRED KNOWLEDGE, SKILLS AND ABILITIES In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines In depth therapeutic and protocol knowledge as provided in company training Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer Strong written and verbal communication skills including good command of English language Excellent organizational and problem-solving skills Effective time management skills Strong presentation skills Effective mentoring and training skills Ability to lead and motivate a culturally-mixed clinical team Ability to manage competing priorities MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor’s degree in a health care or other scientific discipline or educational equivalent; 3 years clinical monitoring and one year in a project leadership role or equivalent combination of education, training and experience   To submit your resume , please sign in...   CLINICAL RESEARCH ASSOCIATES (all levels)    Hays Pharma    All   30/9/2008  Category: Clinical Research   Education:   Position type: Full Time Employee  Experience: 1 year  Area(s) of expertise desired:   Description: Our client, a highly reputable leading global Contract Research Organisation, is looking for Clinical Research Associates to join the team. The purpose of the role is to identify, select, initiate and close-out appropriate investigational sites for clinical studies and to monitor these sites ensuring that the studies are performed in accordance with the SOPs, applicable regulations and ICH-GCP guidelines. ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.   Requirements: Education and qualifications Medical/science background and 1 year previous clinical research experience; Ability and willingness to travel at least 50% of the time; Ability to review and evaluate clinical data; Computer literacy desirable; Good use of English; Good oral and written communication skills.   To submit your resume , please sign in...   Electronics Production Engineer    Megama    Sharon Area, Raa'nana   19/9/2008  Category: Engineering, Medical Equipment   Education: Post-Bachelors, Pre-Masters   Position type: Full Time Employee  Experience: 4 years  Area(s) of expertise desired: Engineering   Description: • New Product Introduction and Transfer to Production. • Subcontractor's selections and support (Turn Key Products and Production). • Production Line Definitions (infrastructures definitions; Jigs and fixtures). • Production Engineering Support (for ongoing issues; Training; Testing etc.). • Manage debugging for new product and for upgrades. • Ongoing support and communicating the marketing abroad   Requirements: • Electronics Engineer– Mast. • At least 4 years proved relevant experience. • Experienced with ERP and PDM systems (Priority – Advantage). • Knowledge in boards’ assembly and SW debugging. • Experienced with international Medical Devices Standards – Adv