http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/senior-research-associate-philadelphia-pa-pa-pennsylvania-200631302.htmFri, 20 Nov 2009 22:08:16 +0000196398Senior Research Associate, Philadelphia, PA No relocation! For consideration, applicants must be located near the Philadelphia, PA area. Description: Under the direction of the Director of the Immunology Laboratory, to promote and coordinate the multiple aspects of the growing research program of immunology Laboratory. The job involves performing diverse and complex clinical research activities including, but not limited to, writing study protocols and other research related documents, maintaining IRB and GCRC approval of study protocols, creating and instituting quality assurance procedures, performing research quality bone age and bone mineral density determinations, data management and quantitative analysis, collaborating in developing innovative research and educational programs, writing manuscripts and grant proposals, coordinating activities in multi-center studies, and serving as an educational resource for the laboratory and the Institution. This position has the potential for the candidate to develop into an independent investigator. Qualifications: MD or Ph.D. or equivalent in Immunology or related field with 2 years of experience in pediatric stress/psychometric biomarkers. Previous experience in cell culture, Elisa and PCR preferred. Ability to function independently in a clinical research setting. Excellent writing skills. Excellent communication skills to interact with staff, parents and children. Ability to handle confidential materials. Ability to handle multiple, time dependent tasks. Excellent organizational skills. Ability to use computers, learn new software applications. Ability to manage data and perform quantitative analysis. Ability to write progress reports and scientific manuscripts. To apply please send your CV and three letters of recommendation to Wendy Rochlin by clicking Apply Now. http://www.newscientistjobs.com/jobs/job/research-scientist-hertfordshire-200645742.htmFri, 20 Nov 2009 17:03:26 +0000196125Lab Support is recruiting Resarch Scientists within a small product development group of an exciting new biotechnology company. The role will be to develop a novel PCR-based medical device for the detection of live cells in clinical samples and will also encompass development of the device to improve sensitivity. MAIN DUTIES AND RESPONSIBILITIES • Sample preparation handling clinical samples, including bacterial and fungal cell culture. • Device development using PCR • Validation studies prior to launch. Minimum Requirements/Qualifications: • BSc/MSc/PHD or equivalent qualifications in a Biosciences subject is required. • Either microbiological or molecular (PCR) based laboratory experience essential. • Experience of working in NHS environment and familiarity with current microbiological testing in hospitals essential. • Experience of working to ISO 9001 and ISO13485 is hihgly desirable. The ideal candidate will be qualified to PhD level or equivalent with substantial microbiological or molecular (PCR) experience. NHS experience and knowledge of current microbiological testing in hospitals is essential. Please apply with full CV outlining your experience in this field and quoting ref CAM-LZG-2011. Please note that candidates without the relevant experience may not be contacted. To apply for this role please call 01223 451021 or email your CV to cambridge@labsupport.co.uk quoting reference number CAM-LZG-2011. Lab Support is unable to employ any candidates requiring a sponsorship to work in the UK and all applicants must be in a position to accept employment without infringement of their immigration status. Lab Support is working as an Employment Business in relation to this role. http://www.newscientistjobs.com/jobs/job/senior-business-development-director-belgium-200645708.htmFri, 20 Nov 2009 16:45:20 +0000196041Director Business Development Europe Our client is a global, full-service clinical research organisation with specialist expertise in cardiovascular, endocrine / metabolic, and oncology research. They have steadily expanded their operations so that they have presence in nearly 40 countries. Company headquarters are located in the USA with European headquarters in Rotterdam, and offices throughout Europe. Due to impressive recent growth they are currently looking to recruit someone to fit into a key role within their Business Development activities. This will be mainly focused in Europe and will report directly to the Executive Director of Business Development in the USA. The main responsibilities will include: • Generating and closing new sales opportunities • Establish and manage the European Business Development team • Developing and managing new and existing customer relationships • Attend key industry conferences • Identify and coordinate meetings with internal operational staff and external Clients • Direct sales activities with internal resources. Person specification: • Extensive experience within a CRO sales environment in Europe • A proven track record within sales • Highly organised, result oriented and customer focused working style • In view of the frequent international contacts, you will have excellent interpersonal, communication and presentation skills This is a fantastic opportunity to join a rapidly growing company with excellent career development opportunities. http://www.newscientistjobs.com/jobs/job/european-associate-marketing-director-diabetes-uxbridge-200645669.htmFri, 20 Nov 2009 16:28:41 +0000195949European Associate Marketing Director - Diabetes Our client is a top 10 Pharmaceutical company who provide innovative medicines globally to help millions of people in their fight against serious diseases such as cancer, heart disease, diabetes, HIV/AIDS, rheumatoid arthritis, hepatitis B and psychiatric disorders. An exciting new opportunity has arisen for a senior, experienced marketer to join their Brand Team with responsibility for Key projects within the diabetes programme. The purpose of the role is to support the EMEA Diabetes Brand Lead in preparing for and optimizing the recent launch of a new diabetes drug by providing input to the European commercialisation strategy, and resource recommendations to Global Marketing. The ultimate aim is to achieve optimal commercialisation and Life cycle management of the brand in Europe. The successful candidate will acquire and apply thorough understanding of the European market in order to identify and optimise launch and life cycle management opportunities for the diabetes brands. Experience Required: • Extensive experience in European/International / U.S. marketing or commercial medical support roles • Demonstrated successful track record of working within high performance, cross-functional or multi geography teams or complex organizations • Knowledge of European pricing and reimbursement systems, payors and healthcare systems • Well developed knowledge and understanding of new product development processes • Developed and implemented marketing plans, including market research, product marketing, new and strategic product planning ideally at a European or International level Knowledge Desired • Mastery of commercial (e.g. marketing, sales and marketing research) and business development (e.g. new product development and introduction, interaction with R&D, business acumen), including overall familiarity with Marketing Excellence processes. • Broad and in-depth understanding of international issues relative to the diabetes therapeutic areas. • Understanding of the brands and diabetes/Metabolics disease area: its competitors, customers and KOLs. • Preferably has established relations with opinion leaders in the disease area of responsibility or has a demonstrated an ability to develop KOLs in other Disease Areas. • Understanding of effective international and matrix working. Additional Competencies required • Proven abilities to develop and maintain strong internal and external relationships • Willingness / ability to travel • Presentation / communication skills This is a really fantastic role to join a top 10 Pharmaceutical company to help manage the launch of a new key drug. If you have the right experience and would like more information please contact Gareth at Talentmark at gareth@talentmark.com or 08450952626. http://www.newscientistjobs.com/jobs/job/biomedical-scientist-london-200645656.htmFri, 20 Nov 2009 16:25:00 +0000195923Lab Support is currently recruiting for a Biomedical Scientist to work for a contract research laboratory based in London. Our client is an established international contract testing company supporting clinical research amongst other industries. They are looking for a HPC registered Biomedical scientist to perform a range of homological and biochemical analysis, this role has excellent potential for the right candidate and an attractive benefits package. The ideal candidate will be HPC registered or have applied for HPC registration, and have experience of having performed a range of Biomedical testing, ideally on a Rosche based system. They will also have a proven track record in either biochemistry or haematology ideally in a hospital setting, but other backgrounds will also be considered. If you do not demonstrate the above criteria in your CV then you will not be considered for this role. To apply for this role please call 01753 623 967 or email your CV to windsor@labsupport.co.uk quoting reference number 2178641. Lab Support is unable to employ any candidates requiring a sponsorship to work in the UK and all applicants must be in a position to accept employment without infringement of their immigration status. Lab Support is working as an Employment Agency in relation to this role. http://www.newscientistjobs.com/jobs/job/health-and-safety-advisor-north-west-north-east-200645387.htmFri, 20 Nov 2009 14:38:16 +0000195387Health and Safety Advisor Up to: £27000 Our client is a public sector organisation in the North East. They are seeking a Health and Safety Advisor to promote a positive health and safety environment and provide working health & safety legislative support to all relevant managers assisting them to comply with their legal health & safety obligations. Key Responsibilities - Formulate and develop health and safety policies for new and existing processes - Advise and assist with the compilation of operational risk assessments. - Carry out health and safety inspections, and produce reports identifying areas of weakness and risk assessments. - Conduct fire risk assessments on all premises and produce reports. - Ensure that all contractors and suppliers comply with health and safety legislation and procedures in order to protect the organisation from harm or loss. To be considered for this role you will need to be a need to be an experienced Health and Safety professional. A background in the public sector would be an advantage. You will need a minimum of NEBOSH certificate and a recognised certificate in Fire Safety and Risk Assessments This role will include travel between regional offices in the North West. http://www.newscientistjobs.com/jobs/job/cdm-co-ordinator-south-yorkshire-200645363.htmFri, 20 Nov 2009 14:25:24 +0000195316Job Title: CDM Co-ordinator Salary: £25000 to £27000 Job Type: Permanent Region: Northern England Description Our client is seeking a fully qualified client focused CDM Co-ordinator to join their dynamic building consultancy based in the North of England To be considered for this role you will need to be an experienced senior professional with construction related qualifications and a minimum of APS. The role includes the opportunity to manage a team within the organisation so leadership and good communication skills at all levels are essential. http://www.newscientistjobs.com/jobs/job/hearing-aid-dispenser-republic-of-ireland-200643907.htmFri, 20 Nov 2009 13:11:32 +0000194626Hearing Aid Dispenser Our client is a leading provider of hearing support and technology in the community who are now planning to develop their presence in the Irish market. With a global presence and an excellent track record of customer focus and care, our client is now planning to recruit a sales professional to grow their business in Ireland. Responsibilities • Administering auditory tests on adults. • Rehabilitation of patients, including counseling them and advising them on wearing hearing aids and hearing tactics. • Advising on the selection, fitting and evaluation of hearing aids. • Offering guidance on maintaining hearing aids. • Visiting patients in their homes and community clinics. • Operating audiometric equipment. • Willingness to participate in general admin/office duties. The Candidate • At least 5 years experience in a similar role. • Relevant degree/certificate in hearing aid dispensing. • Must have a car and full driving license. • Willingness to travel in the greater Dublin area (home visits). • Personality: customer friendly. ************************************************************** For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 4747 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy http://www.newscientistjobs.com/jobs/job/editorial-manager-medical-communications-london-city-200644941.htmFri, 20 Nov 2009 12:59:22 +0000194562Editorial Manager - Medical Communications - London An international Medical Communications agency with has the unrivalled opportunity for an inspirational and dynamic Editorial Manager to head an established and highly experienced editorial team. Leading a team of up to four editorial staff, you will be working across several projects and accounts covering a variety of therapy areas. In this newly created role, you will be responsible for developing and delivering on marketing strategy for pharmaceutical clients and managing budgets, time lines and your team. You will work with the managerial team in order to identify new business opportunities and provide direction for the account. You will also be on hand to provide support to the Editorial Director in order to ensure smooth running of the business at all times. Suitable candidates will have a life science degree and at least 3 years experience gained within either a Medical Communications agency or Medical Publishers. Previous management experience is necessary as is the ability to create and develop successful client relationships. You will possess an exceptional eye for detail and have the ability to portray scientific data clearly and accurately. In return you will have the opportunity to work for an industry leader within Medical Communications. You will have excellent opportunities for career progression and the chance to be part of a successful creative team within an integrated agency environment. A highly competitive remuneration package is on offer. For more information on this fantastic opportunity please contact Louise Breen on 0121 616 3469. Editorial Manager, Senior Editor, Editor, medical communications, medical writing, medical writer, healthcare communications, senior medical writer Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/clinical-research-clinical-research-nurse-jobs-nottinghamshire-nottinghamshire-200644881.htmFri, 20 Nov 2009 12:35:29 +0000194479Flame Pharma Clinical Research Jobs - Clinical Research Nurse Job - Nottinghamshire Nottinghamshire, UK: Competitive Salary Flame Pharma are currently working alongside a leading Clinical Research Organisation to appoint a fully NMC registered Nurse to join their skilled and established team and take on the challenging new role of Clinical Research Nurse in their state of the art facilities in Nottinghamshire. This unique opportunity would offer the successful candidate the chance to further their nursing career by joining an innovative forward thinking company that pride themselves on being World Leaders in early Clinical Development. The Role As a Clinical Research Nurse, reporting to the Director of Clinical Operations, it will be your responsibility to ensure subject safety at all times. In addition, you will ensure study data is collected to a high quality in accordance with ICH-GCP, whilst providing cover for recruitment, screening and the clinic areas The Person The ideal candidate should be fully NMC registered and Degree qualified in general/adult nursing or equivalent with proven post registration experience, preferably gained within a critical care setting and/or clinical research environment. For more information please contact Flame Pharma on 0800 085 0858 or email careers@flamepharma.com Key Words Medical Affairs, RGN, Clinical Research, CRO, Research Nurse, NMC, Clinical Trials, Professional, Clinical Skills, Nottinghamshire, Job, Opportunity, Vacancy This position will be located in Nottinghamshire. http://www.newscientistjobs.com/jobs/job/work-on-a-tropical-island-pharmacovigilance-role-mauritius-200644872.htmFri, 20 Nov 2009 12:27:32 +0000194475With a dreary and depressing winter drawing in, with the prospect of Strictly Come Dancing and the X-Factor finishing who wouldn't want to consider this? (Do I even need to mention the recession?) http://diggtravel.files.wordpress.com/2009/06/9-mauritius1.jpg We are presently working closely with a growing Global Pharma who is seeking an experienced Drug Safety/Pharmacovigilance professional with EU experience. The role will be based in the Mauritius! This is a very unique opportunity and offers a once in a lifetime opportunity to progress your career whilst enjoying the relaxed lifestyle that living on a tropical island can offer. Not to mention the benefits of living and working in a tax haven. The role will involve the effective and accurate collection, database entry and reporting of safety data and you will be responsible for all the operational pharmacovigilance activities for assigned developmental and marketed products. The Drug Safety Officer will also be negotiating and finalizing Safety Data exchange agreements (including monitoring compliance), co-ordinating all ADR investigations, overseeing and clinical or post-marketing surveillance trials, reviewing all training material related to pharmacovigilance. In order to take advantage of this once in a lifetime opportunity you will be experienced within Pharmacovigilance/Drug Safety, ideally over 2 years however candidates with the suitable level of skills outside of this may also be considered. For a confidential discussion and to find out more information about this role please contact the Oliver Donoghue from the Drug Safety Team on 0207 234 0550 or by e-mail to Drugsafety@NonStop-pharma.com http://www.newscientistjobs.com/jobs/job/qp-south-east-200644753.htmFri, 20 Nov 2009 10:53:13 +0000194215Qualified Person (QP) Ref: 16026 Our SE based client are actively looking for a Qualified Person. Duties for this position will include: - - Act as QP for approval of products for release to the market in accordance with regulatory requirements and Codes of Practice. - Undertake QP release for 3rd Parties - Assist QA with respect to corrective and preventative actions - Act as Coach in Solid Dose manufacture and packaging with regards to Quality - Participate and assist with Audits - Communications with QP Team members and QA, reporting quality issues, improvements and changes - Any other assigned activity requiring QP requisite skills - Ensuring Health and Safety procedures are followed, near miss accidents, workstation assessments etc - Ensuring timely product release in accordance with GMP and license requirements Applications are invited from candidates with a BSc / MSc / PhD in a scientific subject together with previous suitable skills and abilities in a Solid Dose manufacturing environment. This is a permanent opportunity, offering a salary of up to £50,000 (depending on skills and abilities) Role: Permanent Location: South Salary: Up to £50,000 For further Science Jobs visit www.sci-search.com http://www.newscientistjobs.com/jobs/job/study-technician-wi-wisconsin-200644694.htmFri, 20 Nov 2009 10:00:49 +0000194133BIOLOGY, ZOOLOGY, ANIMAL SCIENCE and CHEMISTRY GRADS. We have the PERFECT opportunity for you! At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities. Imagine being involved in cutting edge projects that change the course of our industry on a daily basis. At Covance, one of the world's largest and most comprehensive drug development service companies, you will have an opportunity to build an exciting career while you make a direct impact on the lives of millions. We are currently seeking a variety of Study Technicians for our laboratory located in beautiful Madison, Wisconsin, and relocation and interview travel assistance is available! We are seeking study technicians for the following areas: Toxicology In-Life - Collects, documents, and manages pertinent data related to Toxicology studies, including laboratory animal observations, test material administration and sample collection. Pathology - Performs basic necropsy or histology tasks on a variety of laboratory animals. Metabolism In-Life - Collects, documents, and manages pertinent study data, but also tracks the test material as it travels through the body. Studies can include a variety of laboratory animals. Experience in pet stores, animal labs, farms, kennels, breeders, veterinary clinics, or other experience with animals should be indicated on your resume! The minimum education, experience and qualifications for the Technician positions include: A Bachelor's degree in Science or an Associate degree in either Laboratory Animal Technology or Veterinary Technology. Experience may be substituted for education. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. Covance's ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us. Start time 7:30 End time 4:15 Days per week 5 http://www.newscientistjobs.com/jobs/job/team-leader-mlv-pharmaceutical-company-denmark-200641399.htmFri, 20 Nov 2009 09:53:47 +0000194102Team Leader - Måløv - Pharmaceutical company This is your chance to join the world leader in diabetes care and put your personal mark on R&D projects with the powerful potential to lift the quality of life for millions of people around the world. With the creation of the Oral Protein Formulation Unit (OPF), Novo Nordisk is starting its voyage towards the development of Solid Dosage Forms of diabetes proteins for oral delivery. Our ambition is to develop break-through products with orally available versions of insulin and GLP-1. You will be involved in CMC activities for development within protein formulations for oral delivery, covering formulation, process technologies and development, and pharmaceutical-technical tests. Challenges As Team Leader, you will be the focal point for your team. Coaching, set directions and motivating a team of 15 formulation principal scientists, scientists and technicians – as a leader and an expert in solid dosage forms – you will drive the work forward and ensure that your team meet the set goals. Also, you ensure the personal and professional development of the team as a whole as well as the individual team members. You combine your skills as a leader and your knowledge of Solid Dosage Forms. Your overall goal is to contribute to enabling Novo Nordisk quickly to enter clinical trials with our new oral protein formulation concepts. This position is unique as it allows you to work in a field that combines oral Solid Dosage Forms with proteins and peptides. You will be central in the pharmaceutical development and you can look forward to becoming a key part of our international R&D organisation. You will find an abundance of professional and personal development opportunities in this position, additionally you can look forward to collaborating with experts from different fields in an international environment. Qualifications Most importantly, you are an experienced manager and have already proven your excellent leadership skills and your ability to coach and motivate a team. You hold a Master’s degree or a PhD in Pharmacy, Engineering or another relevant scientific discipline and have some years of experience with the formulation of Solid Dosage Forms, process optimisation, mixing, granulation, compression, coating and capsulation as well as pharmaceutical-technical analyses. As you will be working with colleagues from different fields and of different nationalities, it is essential that you have strong communication skills and thrive in an environment where international teamwork is key. In return, we offer you a world of opportunities starting with influencing the lives of millions of people with diabetes worldwide. http://www.newscientistjobs.com/jobs/job/marketing-opportunity-south-west-200644654.htmFri, 20 Nov 2009 09:33:25 +0000194065Are you working within a Life Sciences Laboratory maybe doing Cell Culture? Looking to develop your career in an exciting new direction? PAA is a leading manufacturer and supplier of Cell Culture consumables to the Research, Bioproduction and Diagnostics communities. We are looking for an enthusiastic, creative individual with excellent written and verbal communication skills are a must. You will be involved in all aspects of the marketing process including liaison with product development, creation of online as well as traditional promotional materials, exhibition organisation, pricing and the implementation of new product launches. Interested? If so please send your current cv to our recruitment experts by clicking the Apply Now button below, or call the number listed within the 'View Contact Details' section for more information. Direct applications to PAA will not be considered. http://www.newscientistjobs.com/jobs/job/professional-healthcare-representative-waterbury-ct-ct-connecticut-200643872.htmFri, 20 Nov 2009 04:01:43 +0000193740The Professional Healthcare Representative may have a variety of roles, such as the responsibility for sales targets and physician relationships within a specific geography. The Professional Healthcare Representative must demonstrate a strong understanding of necessary disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease management information to customers. The Professional Healthcare Representative will provide the most current information pertaining to Pfizer products and their approved indications in a manner which will ensure the appropriate use of these products and achieve the business potential of the territory. Qualifications: • Bachelors Degree • Demonstrated business acumen • Proficiency using sales data/call reporting software/applications • Outside sales experience preferred Functional / Technical Skills can include: • Promotes broad portfolio of products (up to 9 total); Strong knowledge of disease states, therapeutic areas, and products • Drives sales in assigned accounts/with assigned physician targets • Cultivates relationships with KOLs; build lasting relationships with priority doctors • Assesses needs of target physicians; Addresses needs with responsive approach, targeted skills, and appropriate resources • Develops superior selling, technical and relationship building skills • Executes priorities of District Business Manager Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residence and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. HOW TO APPLY: Please copy and paste the following URL into your browser address bar: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R6378125807956 http://www.newscientistjobs.com/jobs/job/medical-writer-medical-communications-london-city-200644372.htmThu, 19 Nov 2009 17:55:29 +0000192927Medical Writer - Medical Communications - London A specialist medical communications agency based in the London has a number of outstanding opportunities for Medical Writers of all levels to join their pioneering team. This company is unique and boasts some of the best product knowledge in the business, which is apparent in the production of some of the industry's most technically accurate material. This is a fantastic opportunity to cultivate your career in a highly reputable company. As a Medical Writer you will be responsible for writing high quality materials over a vast range of therapy areas and communication programmes. You will have the opportunity to lead projects and be the main point of contact for high profile clients. This is a multi-functional role with the opportunity to explore all areas of the Medical Communications industry. Skills Suitable candidates for the Medical Writer position will ideally have at least 18 months experience within a Medical Communications agency. Writers of a senior level will have at least 3 years experience. A life science degree is essential along with excellent written and oral communication skills. Candidates must be well organised and have an exceptional eye for detail. In return you will have the opportunity to work in a friendly, informal environment and enjoy a competitive salary and benefits package. There are superb career prospects within this company and with the business growing from strength to strength the opportunities are endless! For more information please contact Louise Breen on 0121 616 3469 Medical writer, medical writing, medical communications, healthcare communications, medical education, medical marketing communications, scientific communications, healthcare PR, senior medical writer, medical editor Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/global-brand-access-associate-director-basel-200644371.htmThu, 19 Nov 2009 17:53:16 +0000192926My client is one of the worlds leading Pharmaceutical companies and we are currently recruiting for an Associate Director within their Global Brand Access team based at their Global HQ in Basel. JOB PURPOSE Lead the marketing team for all payer related strategies. Support the Brand Director of a priority brand or group of brands with high quality timely pricing and market access input. Responsible to finalize development of the Global Pricing & Market Access Strategy, incl. innovative pricing arrangements, based on robust understanding of payers & their decision making systems (worldwide and in key markets). Prepare tools to achieve and maintain broad market access. Drive execution of market access strategy through global operational market access plan. MAJOR ACCOUNTABILITIES Lead the marketing team for all payer related strategies ("promotion to payers") for a priority brand or group of brands Finalize development & gain support for Global Pricing & Market Access Strategy, including innovative pricing arrangements and tools for accelerating and broadening access. Refine "Optimizing Brand Value" including payer value proposition, pricing & reimbursement strategy based on emerging evidence (customer insights, competitive environment, clinical trial results, economic analyses) Drive global payer interactions. Generate payer insights & validate payer value proposition (PREB as prioritized through IFB). Focus on national, regional and local pricing, reimbursement and coverage decision makers Conduct quantitative pricing research to define value optimizing pricing strategy Define initial launch sequence Advise clinical development organization on clinical and economic evidence needed to support payer value proposition Support worldwide market access efforts (product or product group specific): achieve target price, reimbursement and listing, proactively address market access needs, gather data and provide input on pricing & market access related topics into International marketing plan as well as other key documents. Lead payer topic in Value Demonstration and Commercialization Team (VDCT) Interact with Global Product Advocacy for preparing market access; interact with Global Health Economics & Outcomes Research to align Value Dossier with pricing & reimbursement strategy Improve knowledge in Brand Team on payer and pricing aspects Ensure alignment with Strategic Pricing & handover of global pricing & market access strategy to Market Pricing Support region/key CPOs in developing Market Access Operational Plans Deliver brand access toolkit to support country market access preparation Participate in LRR Share best practices and coordinate the communication of market access related information across the organization. Conduct competitive assessments, identify trends, opportunities and threats on pricing & market access issues, (worldwide and in key local markets) and propose corresponding measures. EDUCATION / EXPERIENCE Minimum degree acceptable: University degree in Science and/or degree in Business Desirable degrees: Marketing MBA, advanced degree (master or PhD) in economics, medicine or pharmacy Ideal experience: Global Marketing experience in brand management and pricing for a minimum of 5 years, thereof minimum of 2 years each in pricing and brand management. Experience in one of the big Pharma companies. Extensive local payer and market access experience http://www.newscientistjobs.com/jobs/job/medical-writer-medical-communications-cheshire-cheshire-200644367.htmThu, 19 Nov 2009 17:46:50 +0000192921Medical Writer - Medical Communications - Cheshire A global leader in Medical Communications has an excellent opportunity for a Medical Writer to join their Cheshire offices. With a strong client base of international clients you will be responsible for the execution of written Medical Education materials as well as publication planning, congress management and brand / corporate materials. Reporting directly to the Scientific Director as a Medical Writer you will be responsible for monitoring and managing your own projects. You will enjoy researching and working across a variety of therapy areas in addition to maintaining an up to date product portfolio. You will produce clear, accurate and grammatically sound work and also have the opportunity to contribute to creative ideas in order to pitch for new business. Suitable candidates for the Medical Writer role will ideally possess a life science degree with a higher qualification being a distinct advantage. Experience within a Medical Communications agency or similar environment is highly desired but not essential. The ability to write communication items to a variety of target audiences and liaise successfully with clients and KOL's is fundamental to this role. In return you will have the opportunity to develop your career as a Medical Writer in a fresh and growing agency. This company is thoroughly committed to career development and offers tailored development programmes to ensure this materialises. If you would like more information then please contact Louise Breen on 0121 6163469 Medical writer, medical writing, medical communications, medical education, healthcare communications, healthcare PR, scientific communications editor senior editor senior medical writer Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. http://www.newscientistjobs.com/jobs/job/asbestos-and-air-testers-london-200644303.htmThu, 19 Nov 2009 16:45:39 +0000192840Lab Support are currently recruiting an Asbestos and Air Tester to work for a contract testing lab in SW London. The successful candidate will be required to perform asbestos and air sampling in a range of locations around London. Due to the field based nature of this role good communication and time management skills will be required. To be considered for this position you will have successfully passed BOHS P403 and P404, and have a current clean full UK driving licence. The ideal candidate will be self motivated with good awareness of Health and Safety legislation. If you do not demonstrate the above criteria in your CV then you will not be considered by Lab Support for this role. To apply for this role please call 01753 623 967 or email your CV to windsor@labsupport.co.uk quoting reference number 2178929. Lab Support is unable to employ any candidates requiring a sponsorship to work in the UK and all applicants must be in a position to accept employment without infringement of their immigration status. Lab Support is working as an Employment Agency in relation to this role.