better Printing and Publishing Job at Biotechnology Pharmaceuticals

Business Title Senior Medical Writer Requisition ID 18307BR Job Category Clinical Research Locations UK - Leeds Shift 1 Job Posting Senior Medical Writer The successful candidate will be responsible for the preparation and the coordination of the development of study protocols and clinical study reports, including investigator's brochures, and other documents as needed. They will act as a scientific leader of the Pharmacometrics project team on the reporting of Phase I /II studies. Duties and Responsibilities

Business Title Medical Writer II Requisition ID 19407BR Job Category Biotechnology/Pharmaceutical Locations USA - Madison, WI Shift 1 Job Posting 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. Covance

Business Title Associate Medical Writer Requisition ID 18308BR Job Category Clinical Research Locations UK - Leeds Shift 1 Job Posting Associate Medical Writer The successful candidate will assist Medical Writers in the preparation and background writing of Clinical Study Reports and clinical study protocols. Duties and Responsibilities: . Communicate with internal staff and the study site contacts, to obtain all relevant information needed to adhere to the project schedule. . Assist Medical Writers in the preparation

Business Title Medical Writer I Requisition ID 18147BR Job Category Clinical Research Locations USA - Madison, WI Shift 1 Job Posting 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. Covance's ongoing

Business Title Manager, Publishing, Editing & Report Quality (PERQ) Requisition ID 16364BR Job Category Biotechnology/Pharmaceutical Locations USA - Princeton, NJ Shift 1 Job Posting TheManager of Publishing, Editing & Report Quality (PERQ)is expected to ensure quality control and efficiency in the production of clinical documents for electronic regulatory filing. The responsibility of this position includes liaising with document contributors and managing the retrieval and preparation of clinical documents

Business Title Senior Medical Writer - CLINICAL RESEARCH Requisition ID 14600BR Job Category Regulatory Affairs Locations USA - Princeton, NJ Shift 1 Job Posting 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

Ben Venue Laboratories (BVL) is currently seeking a Scientific Writer II for their Manufacturing, Science and Technology (MST) group for their state-of-the-art pharmaceutical manufacturing facility in Bedford, OH. Position Summary:Employee will be responsible for designing, writing and maintaining technical reports that detail specific activities, studies and procedures developed or modified in the MST department. - Writes, re-writes or edits technical documents to communicate clearly & effectively technical

Editor Requisition ID: 56224 Position: Full-Time Regular Open date: Nov 2, 2009 9:49:03 PM Functional area: Marketing Location: Philadelphia, Pennsylvania Raleigh/Durham, North Carolina Required degrees: Bachelor's Level Degree Experience required: 2 years Relocation: No Basic qualifications: Bachelor's Degree in English, Writing or related field; 2 years' experience proofreading and editing materials and/or pharmaceutical promotion; Demonstrated understanding of grammar, spelling, punctuation and syntactic

Medical Writer / Sr Medical Writer Job Type: Regular Full-Time Location: Seattle, WA Job Description: Dendreon is seeking a Medical Writer who will lead the preparation of clinical reports, summary documents, package inserts and other documents that may be submitted to the Food and Drug Administration or other regulatory agencies. A self-motivated individual with strong oral and written communication skills is needed for this critical position. General Summary: Researches, writes and edits pre-clinical

Summary Lead clinical writer of medical writing projects pertaining to clinical drug development in an assigned therapeutic area. Prepare high-quality clinical documents (eg, patient narratives, clinical study reports, integrated summaries) in compliance with regulatory requirements and Forest style/format. Participate as an active member of clinical study teams and work in collaboration with cross-functional areas. Reports to Senior Manager/Manager, Medical Writing. Duties and Responsibilities 1.Write

Requisition ID: 16390 Position Title: Senior Copywriter Working Location: Westborough, MA Required Experience: See Description Required Education: See Description Required Travel: 0 Job Description Genzyme Genetics is an award-winning national provider of highly sophisticated diagnostic testing, including prenatal, postnatal and neonatal as well as oncology testing. We are one of the largest diagnostic locations around the United States and a growing international portfolio. We also provide Genetic

Meridian is a fully integrated life sciences company that manufactures, markets and distributes a broad range of innovative diagnostic test kits, purified reagents and related products and offers biopharmaceutical enabling technologies. Summary Description: The Document Control Specialist I is responsible for providing different levels of support to the production and management team. This may involve preparing labels, reviewing document drafts, assisting with document retrieval, processing change request

Manages publication team leads for all Shire products Defines publication lead roles and responsibilities Ensures consistency and compliance in publication policies and practices across therapeutic areas Manages overall publication budgets and forecasting for each product 30People and relationship management Direct management of all Publication Leads Manages relationships with publication vendors in conjunction with publication leads Communicates with BU contacts, TA heads and customers

Manages publication team leads for all Shire products Defines publication lead roles and responsibilities Ensures consistency and compliance in publication policies and practices across therapeutic areas Manages overall publication budgets and forecasting for each product 30 People and relationship management Direct management of all Publication Leads Manages relationships with publication vendors in conjunction with publication leads Communicates with BU contacts, TA heads and customers and ensures

Ben Venue Laboratories (BVL) is currently seeking a Scientific Writer II for their Manufacturing, Science and Technology (MST) group for their state-of-the-art pharmaceutical manufacturing facility in Bedford, OH. Position Summary: Employee will be responsible for designing, writing and maintaining technical reports that detail specific activities, studies and procedures developed or modified in the MST department. - Writes, re-writes or edits technical documents to communicate clearly & effectively

Senior Medical Editor Job ID NJS09-31 Working Location NJ, Bridgewater Employment Status Full-Time Required Travel No Required Experience Not Indicated Required Education Not Indicated Position Description This position manages the delivery of a full range of editorial services, including medical editing, copy editing, proofreading, and fact verification of pharmaceutical marketing materials, internal and external presentations, and corporate communications, from initial CCC submission through final approval

At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world s largest and most respected contract research organizations. Our clients are a Who s Who of the pharmaceutical and biotechnology industry. If you re looking for a diverse and stimulating work environment, you'll find it at Covance. The Medical Writer is responsible for the production of study protocols, clinical study reports (CSRs), Investigator

Promotional Copywriter Requisition ID: 55909 Position: Full-Time Regular Open date: Nov 4, 2009 12:00:00 AM Functional area: Other Location: Philadelphia, Pennsylvania Required degrees: Bachelor's Level Degree Experience required: 3 years Relocation: Not Indicated Basic qualifications: -Bachelor's degree -Minimum of 3 years copywriting experience for the pharmaceutical/healthcare industry(ad agency and/or corporate) Preferred qualifications: -Expertise in creating print promotional pieces such as sales aids

Overview: Teva Pharmaceuticals is the leading global generic pharmaceutical company employing 26,000 people worldwide. The company's aggressive growth strategy has positioned Teva as a top 20 global pharmaceutical company with plans to be Top 10 in the coming years. Teva is the largest manufacturer and distributor of pharmaceuticals in the world. Teva USA is a wholly-owned subsidiary of Teva Pharmaceutical Industries Ltd., Israel's largest pharmaceutical manufacturer operating globally in

JOB TITLE: Copywriter III At Cardinal Health, we're developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities. Function: Communications Family: Copywriting What Copywriting contributes to Cardinal Health Copywriting is responsible for developing copies designed to support the business objectives and ensuring alignment with corporate strategy and messaging

Promotional Copywriter Requisition ID: 55909 Position: Full-Time Regular Open date: Nov 2, 2009 9:39:27 PM Functional area: Other Location: Philadelphia, Pennsylvania Required degrees: Bachelors Degree Experience required: 3 years Relocation: Not Indicated Basic qualifications: -Bachelor's degree - 3 years copywriting experience for the pharmaceutical/healthcare industry(ad agency and/or corporate) Preferred qualifications: -Expertise in creating print promotional pieces such as sales aids, brochures, slim

Job ID: NJS09-31 Position Title: Senior Medical Editor Working Location: NJ, Bridgewater Employment Status: Full-Time Required Experience: Not Indicated Required Education: Not Indicated Travel Required: No Job Description: This position manages the delivery of a full range of editorial services, including medical editing, copy editing, proofreading, and fact verification of pharmaceutical marketing materials, internal and external presentations, and corporate communications, from initial CCC submission

JOB TITLE: Copywriter III At Cardinal Health, were developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities. Function: Communications Family: Copywriting What Copywriting contributes to Cardinal Health Copywriting is responsible for developing copies designed to support the business objectives and ensuring alignment with corporate strategy and messaging

Senior Medical Writer Location Rockville, MD Job ID 2721 Employment Status Full-Time Regular Required Experience 2-5 years Required Education Bachelors Degree or Equivalent Required Travel No Relocation Available Yes Summary/Description Human Genome Sciences (HGS)is a biopharmaceutical company with approximately 800 employees and world-class R&D and manufacturing facilities based in Rockville, MD. We have three promising products in late-stage development - one, raxibacumab, already commercialized

Requisition ID: 16267 Position Title: Quality Documentation Supervisor Working Location: Framingham, MA Required Experience: 5 to 8 Required Education: Bachelors Degree Required Travel: 0 Job Description Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzyme s people and culture have been consistently recognized for excellence

10273 Senior Medical Writer Job ID #:868 Location:South San Francisco, CA Functional Area:Biotechnology Department:Regulatory Affairs Position Type:Not Indicated Education Required:Not Indicated Experience Required:Not Indicated Relocation Provided:

Senior Web Copywriter (WP) Job Type: Full-Time Location: Rockville, MD Job Description: Function of the Position: This is an individual contributor role responsible for writing and developing Web content that establishes a strong online presence for USP and its programs, products, and services. The incumbent will be responsible for writing, editing, and updating the Web site, assist in maintaining Web writing standards, style guidelines, and content plans, and act as a primary advocate for improving and evolving

A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us the most rewarding employer in our field. Scientific Publisher Business Unit:NIBRDivision:NIBRCompany/Legal Entity:USA Novartis Pharmaceuticals

Publishing Specialist, Regulatory Operations Requisition #: 09-4307 # Positions: 1 Location: US-PA-North Wales Experience (Years): 2 Category: Regulatory Affairs - Regulatory Affairs Apply for this job: Your application choices are: Apply for this jobonline Refer a friend to this job More information about this job: Overview: Teva Pharmaceuticals is the leading global generic pharmaceutical company employing 26,000 people worldwide. The company's aggressive growth strategy has positioned Teva as a top

My company shares my passion for helping to improve human health around the world.' 'This is My MedImmune.' Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity

Human Genome Sciences (HGS) is a biopharmaceutical company with approximately 800 employees and world-class R&D and manufacturing facilities based in Rockville, MD. We have three promising products in late-stage development one, raxibacumab, already commercialized with sales to the U.S, Government and two moving toward commercialization. BENLYSTA (formerly LymphoStat-B ) has successfully met its primary endpoint in the first of two Phase 3 trials in systemic lupus, and we expect to have results of the second

Req Number: 1607 Title: Scientific Writer Division: Development Location: Tarrytown, N.Y. Description: Specific plans and justifications: Full-time employee in the Preclinical Development and Protein Science group to author various reports and regulatory documents in support of all preclinical development programs, including INDs, Investigator Brochures, FDA Briefing Packages, sample analysis reports, pharmacokinetic and toxicokinetic reports, and other written documents, as determined by management. The ideal

Overview: Teva Pharmaceuticals is the leading global generic pharmaceutical company employing 26,000 people worldwide. The company's aggressive growth strategy has positioned Teva as a top 20 global pharmaceutical company with plans to be Top 10 in the coming years. Teva is the largest manufacturer and distributor of pharmaceuticals in the world. Teva USA is a wholly-owned subsidiary of Teva Pharmaceutical Industries Ltd., Israel's largest pharmaceutical manufacturer operating globally in

DePuy Spine Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Document Management Supervisor, located in Raynham, MA. DePuy, Inc. - Develops and markets products under DePuy Orthopaedics, Inc., DePuy Spine, Inc., Codman & Shurtleff, Inc. and DePuy Mitek. Among these are products for reconstructing damaged or diseased joints; repairing and reconstructing traumatic skeletal injuries; facilitating the treatment of spinal disorders and deformity; surgical treatment of neurological and

Advion BioSciences is a leading provider of bioanalytical services to the pharmaceutical and biotechnology industries, and an innovator of products for the life sciences. With our corporate headquarters located in Ithaca, NY, our casual yet professional workplace offers all the advantages of working in a small company where your contributions and involvement are noticed. We are currently seeking a Technical Writer to join our staff. The Technical Writer will produce final bioanalytical and validation reports

Title: IT Technical Writer Location: MD Gaithersburg - Corporate Headquarters Req: 02070 Position Summary: Major Duties and Responsibilities (including supervising others): For internal IT users and external MedImmune business departments: o Writes edits revises formats/reformats and reviews: business process infrastructure and standards documents (work flow process maps policies operational procedures work instructions) reference and user guides (manuals online help) release notes technical and system specifications

Kendle International Inc. (Nasdaq: KNDL) is a leading global clinical research organization providing the full range of early- to late-stage clinical development services for the world's biopharmaceutical industry. Our focus is on innovative solutions that reduce cycle times for our customers and accelerate the delivery of life-enhancing drugs to market for the benefit of patients worldwide. As one of the fastest-growing global providers of Phase I-IV services, we offer experience spanning 99 countries, along

The Forest Research Institute (FRI) a wholly-owned subsidiary of Forest Laboratories, Inc. drives the scientific research and development behind Forest s top-quality therapies that help people lead healthier, more fulfilling lives. With operations in Jersey City, NJ and on Long Island, plus clinical trial personnel across the country, the Institute s highly skilled professionals enable Forest to license compounds at virtually any stage from preclinical development to products that are ready for FDA review and

At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world s largest and most respected contract research organizations. Our clients are a Who s Who of the pharmaceutical and biotechnology industry. If you re looking for a diverse and stimulating work environment, you'll find it at Covance. The Manager of Publishing, Editing & Report Quality (PERQ) is expected to ensure quality control and efficiency in the

Title: Principal Medical Writer I Location: MD Gaithersburg - Corporate Headquarters Req: 02041 Position Summary: Major Duties and Responsibilities (including supervising others): Under minimal or no supervision writes and edits clinical study reports protocols informed consent forms and other clinical and regulatory documents including Investigator Brochures and annual reports. Leads the preparation of briefing documents INDs and other major submissions (BLAs MAAs) as needed. Leads the process of critical

Title: Medical Writing Publications Manager Location: MD Gaithersburg - Corporate Headquarters Req: 01879 Position Summary: Major Duties and Responsibilities (including supervising others): Ensures the timely presentation/dissemination of clinical data from investigational pipeline products according to budget timelines strategic publication plans and tactical approaches. Ensures that strategically aligned scientific communication points are delivered and that statements and conclusions in publications

Publishing Specialist, Regulatory Operations Requisition #: 09-3812 # Positions: 1 Location: US-NJ-Woodcliff Lake Experience (Years): 2 Category: Regulatory Affairs - Regulatory Affairs Apply for this job: Your application choices are: Apply for this jobonline Refer a friend to this job More information about this job: Overview: Teva Pharmaceuticals is the leading global generic pharmaceutical company employing 26,000 people worldwide. The company's aggressive growth strategy has positioned Teva as a

Title Documentation Technician II Department Drug Regulatory Affairs Job Type Full Time Job Category Biotechnology and Pharmaceutical Location Connecticut-Danbury/Bridgeport City Ridgefield Job Description Boehringer Ingelheim is currently seeking a talented and innovative Documentation Technician to join our Drug Regulatory Affairsdepartment located at our US headquarters in Ridgefield, CT. As a Documentation Technician, you will Perform assigned functions related to the documentation, archiving and management

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. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! Currently

Document Control Administrator I/II Job Type: Regular Full-Time Location: Morris Plains, NJ Job Description: Dendreon is seeking a highly motivated individual as a Document Control Administer I/II in our Quality Assurance department at the NJ Immunotherapy Manufacturing Facility. This is a team of grounded and diligent people who are committed to ensuring our systems are everything they should be to support our company mission. This is an excellent opportunity for someone looking to learn and grow in their

Senior Webwriter/Copywriter Tracking Code 1155 Job Description **When applying for this position please note that we request 3 writing samples of your work.* During Step 3: Profile Attachment - please use the upload file button to attach additional files/docs as necessary. JOB OBJECTIVE:As part of a cross-functional team, partner with web team members, scientific communications writers, graphic designers and product managers to develop web content in a collaborative environment. ESSENTIAL DUTIES: 1. Collaborate

Celgene Corporation is committed to delivering innovative therapies designed to improve the lives of patients worldwide. We are a global biopharmaceutical company with operations in more than 60 countries that is helping to turn incurable cancers into chronic, manageable conditions. We are seeking talented professionals as we continue to grow and advance our efforts in oncology and hematology. If you d like to join a company where you can make a difference, please consider the Celgene family. Technical

Medical Writer Job Code :HRReq004140 Division :AmerisourceBergen Corporation Location :Alpharetta GA US Job Type :Full Time Career Level :See Job Description Below Education :Please Refer To Job Description Category :Biotechnology and Pharmaceutical Job Description : Work Location: Alpharetta, GA Shifts: AM Positions Available: 1Position Summary Under general direction of the Vice President, Medical Affairs & Compliance Officer, the incumbent will be responsible for assisting in the development of medical education

Title Scientific Writer II Manufacturing, Science & Technology Department Product Development Job Type Full Time Job Category Science/Research & Development Functional Unit Ben Venue Location Ohio-Cleveland City Bedford Our Culture In a world where business is driven by short term financial goals, Ben Venue Laboratories is truly a company with a different philosophy. As a Boehringer Ingelheim Company, one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain

Senior Document Control Administrator I/II Job Type: Regular Full-Time Location: Morris Plains, NJ Job Description: We are seeking a highly motivated individual as a Senior Document Control Administrator in our Quality Assurance department. This is an excellent opportunity for someone to learn and grown in their GMP Document Control experience. Under Quality Management, this individual will be responsible for leading and supporting efforts of Quality Assurance/Document Control: Identify and implement document