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Medical expert |
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Category: |
Life Sciences, Medical Management, Regulatory Affairs
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Education: |
Doctorate |
Position type: |
Full Time Employee |
Experience: |
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Area(s) of expertise desired: |
Clinical Research, Materials/Inventory Control, Medical Affairs, Medical Records, Medical Writing, Pharmacology
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Description: |
ROLE AND RESPONSIBILITIES
The candidate will model, collect and write information of medical and wellness conditions, manage dictionaries and ontologies to help categorize diseases and phenotypes and will be involved in the definition of scope and requirements for the medical project. Responsibilities are as following:
• Definition of user cases and database model for the Medical Navigator project.
• Designation of relevant data sources available for implementation.
• Work with bioinformatics and software teams to model the medical information and define requirements.
• Writing of medical content for specific diseases, health conditions, risk factors, wellness and more.
• Definition of the QA process and SOP for medical content implementation.
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Requirements: |
• MD- a MUST
• Clinical experience
• English at mother tongue level
• Experience working with biomedical databases – an advantage
• Excellent and demonstrated scientific writing skills
• Creative, initiative and ambitious candidate
• Details oriented
• Collaborative team member with good communication skills
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Medical Director |
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Category: |
Management/Executive, Medical Management, Medical Equipment, Healthcare
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Education: |
Doctorate |
Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
Clinical Research, Medical Affairs, Medical Device, Ophthalmology, Regulatory Affairs, Research, Start-Up, Surgery
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Description: |
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Requirements: |
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Clinical Research Physician |
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Category: |
Clinical Research, Management/Executive, Medical Management, Healthcare
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Education: |
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Position type: |
Full Time Manager |
Experience: |
No experiece |
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Area(s) of expertise desired: |
Academic, Internal Medicine, Oncology
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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.
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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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Medical Director (9594) |
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Category: |
Management/Executive, Medical Management, Pharmacy/Pharmacology
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Education: |
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Position type: |
Full Time Executive |
Experience: |
5 years |
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Area(s) of expertise desired: |
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Description: |
Responsibility for global medical affairs of marketed innovative product:
work with investigators, clinical associates, marketing and legal to ensure timely execution of phase IV clinical studies.
Development of global Key Opinion Leader relations.
Lead and/or support meeting and congresses, including medical congress symposia, expert meetings, advisory boards and internal meetings.
Preparation and/or review of Medical and Marketing materials.
Responses to medical questions from market.
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Requirements: |
Requirements:
MD with 5-10 years of experience which includes experience in the pharmaceutical or Biotechnology Company.
Experience in a Global environment and/ or a previous similar role - a big advantage
Experience in leading clinical trials
MBA or business background - an advantage
Mother tongue level English
Excellent communication and presentation skills
Excellent analytical skills
Ability to work well in a global, complex, multi-interface structure
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Director, Manufacturing |
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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
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Education: |
Bachelors |
Position type: |
Full Time Manager |
Experience: |
10+ years |
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Area(s) of expertise desired: |
Bioanalytical Services, Biology, Manufacturing/Production
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Description: |
Summary
This position is responsible for the technical oversight of biomanufacturing activities at contract manufacturing organizations associated with the production of critical raw materials, Drug Substance and Drug Product.
Responsibilities
• Execute on time and cost the Manufacturing Supply Forecasts through oversight of third party manufacturers based in Japan, Israel and the US : Act as Person in Plant during manufacturing campaigns
• Conduct technical audits of manufacturing operations to identify opportunities for Continuous Improvement at third party manufacturers
• Technical review of batch documents
• Trouble shoot manufacturing issues and support QA in Deviation and CAPA activities
• Support QA in the technical review of Change Requests
• Assist the Chief Technology Officer in the development of budgets
• Provide data to populate the KPI program for Manufacturing
• Other projects and assignments as required.
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Requirements: |
Requirements
• BS Degree, in either bioengineering or a biological science.
• Fifteen-plus years experience in manufacturing of biological products
• Five-plus years in the management of biopharmaceutical manufacturing operations.
• Excellent communication skills in Hebrew, both oral and written.
• Profound knowledge of GMP requirements associated in biomanufacturing in the US and Internationally.
• Knowledge of the engineering aspects of biopharmacecutical manufacturing plants
• Experience working with CMO's
• Goal oriented with a problem solving mindset
• Proficiency with computers and major software packages, e.g. Microsoft Excel, Outlook, Powerpoint, Project
• Excellent communication skills in English, both oral and written.
• Travel - 25%
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Junior Sales Representative Surgical |
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Category: |
QA - Quality Control, Biotechnology, Engineering, Chemistry, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
3 years |
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Area(s) of expertise desired: |
Medical Affairs, Medical Device, Sales
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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. We’re 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
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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, you’ll 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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CEO |
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Category: |
Biotechnology, Medical Management
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Education: |
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Position type: |
Full Time Employee |
Experience: |
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Area(s) of expertise desired: |
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Description: |
General responsibility for company’s activities
Develop and plan company’s targets, goals, assignments and business plan in order to maximize company's achievements
Capital raising
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Requirements: |
MBA
PHD\ MD - preferably in the field of Gynecology\ Immunology
3+ years of experience in senior management in the field of Biomedical in general and clinical researches and pharma specifically
Business orientation
Proven experience in capital raising
Experience in start-up/ incubators companies
Excellent communication skills
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CRA |
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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
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Education: |
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Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
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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.
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Requirements: |
MD
Fluent official language of the country
English, written and spoken, upper intermediate
PC user
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Medical Advisor-Greece |
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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
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Education: |
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Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
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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.
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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.
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Clinical Research Associate/Senior Clinical research associate- office/home based |
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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
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Education: |
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Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Clinical Research
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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.
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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.
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