better Arts Media Job at Biotechnology Pharmaceuticals

Senior Medical Writer Job Type: Full-Time Location: Cambridge, MA Job Description: The Senior Medical Writer is responsible for writing and editing Clinical Development documents, including but not limited to clinical protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, presentation materials, and publications to medical journals. The Senior Medical Writer will collaborate with Regulatory Affairs and other departments to prepare clinical

Medical Writer Req. Code : 1543 Location : MORRISVILLE NC US 27560 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Medical Writing Job Description : AAIPharma is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies to meet exciting drug development challenges. We are seeking candidates for the following

Our client is one of the world's largest energy companies, providing its customers with fuel for transportation, energy for heat and light, retail services and petrochemicals products for everyday items. They require a Document Controller on a contract basis (2 years approx) to work in their Houston branch. - The ideal candidate must have between 3-8 years experience. - Salary may be negotiable depending on experience - Full benefits package supplied through Orion *US, Canadian

Position Title Art Director Business Division Global Pharmaceutical Business Country U.S.A. Location NJ Kenilworth Job Description Develops and produces high level, quality visual core concept material. Major activities and responsibilities include but are not limited to: - Creates high quality creative visual content and generates new and innovative ideas by collaborating with internal staff, utilizing personal creativity, skills and experience to create a broad range of concept advertising, sales promotion

Position Title Copywriter Business Division Global Pharmaceutical Business Country U.S.A. Location NJ Kenilworth Job Description Develops and produces high level, quality core concept written material. Major activities and responsibilities include, but are not limited to: - Creates high quality creative content and generates new and innovative ideas by collaborating with internal staff, utilizing personal creativity, skills and experience to create a broad range of written concept advertising, sales promotion

Clinical Science - Medical Writer/Sr. Medical Writer Tracking Code 661-07-02 Job Description Responsibilities include, but are not limited to, the authoring and editing of scientific and medical documents required during the drug development process, this includes, but is not limited to, IND, NDA and BLA sections, Common Technical Document, Investigator Brochure, Protocol, Protocol Amendments, Informed Consent Documents, integrated clinical and statistical Clinical Trial Reports, IND Annual Reports, journal

Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results, not formality

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

JOB TITLE Senior Medical Writer - Discovery/Translational Research Requisition Number 5600BR Department Name Translational Research Location Cambridge, MA POSITION SUMMARY Member of the Translational Research department, working with discovery scientific staff to write and edit technical reports and the scientific content of regulatory documents. DUTIES & RESPONSIBILITIES The person in this role will be responsible for supporting the scientific work for a wide variety of preclinical and clinical development

JOB TITLE Medical Writer II - Clinical Requisition Number 5317BR Department Name Medical Writing Location Cambridge, MA POSITION SUMMARY Provides writing and editing support to other clinical writers. Independently writes clinical protocols, reports, and investigator brochures. DUTIES & RESPONSIBILITIES Fully edits clinical/regulatory documents. Participates in reviewing, editing, and creating boilerplate and templates. Acts as recognized technical resource for peers. Further improves operational procedures

JOB TITLE Medical Writer I - Drug Safety & Disposition Requisition Number 5440BR Department Name Drug Safety & Disposition Location Cambridge, MA POSITION SUMMARY Medical Writers are critical to the success of the Nonclinical Writing group and are primarily responsible for editing nonclinical study reports and submission sections, as well as timeline management related to those documents. DUTIES & RESPONSIBILITIES Edit and revise nonclinical study reports, protocols and accompanying sections of global regulatory

For over 25 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. We have helped over 800 clients to develop and launch some of the most important drugs and

Learn more about Alexion Pharmaceuticals, Inc.View All Alexion Pharmaceuticals, Inc. Opportunities About Us:Alexion Pharmaceuticals is a leading American biotechnology company that is preparing to launch its first commercial product. We were formed in 1992, listed on NASDAQ in 1996, and now employ 250 people at our Cheshire headquarters, San Diego research and discovery subsidiary, and recently-established European headquarters in Paris. We expect to begin selling eculizumab as a treatment for nocturnal paroxysmal

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

For over 25 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. We have helped over 800 clients to develop and launch some of the most important drugs and

We are seeking a talented and motivated Junior Graphic Designer to join our creative services team. Duties include designing and performing production for brochures, advertisements, displays, and other POP materials. Responsibilities: Utilize creativity designing and performing production for brochures, advertisements, displays, and other POP materials. Creating designs according to press specifications and branding guidelines, preparing files for vendors, printing proofs, and researching stock

Several of our NYC medical communications clients are seeking strong medical writers for their growing interactive business which will support their pharmaceutical clientele.. Job Requirements: -2+ years experience as a Medical Writer in a pharmaceutical advertising agency or medical education company -must have very strong Power Point (slide development) experience -strong interactive writing experience (web sites, audio scripts, video scripts, etc) -experience in any or all of the following therapeutic

NBTY is a leading vertical integrated U.S. manufacturer and distributor of a broad line of high-quality, value-priced nutritional supplements in the United States and throughout the world. We are seeking a talented and motivated Junior Graphic Designer to join our creative services team. Duties include designing and performing production for brochures, advertisements, displays, and other POP materials. Responsibilities: Utilize creativity designing and performing production for brochures, advertisements

Two of our NYC medical communications clients are seeking strong medical writers for their growing interactive business which will support their pharmaceutical clientele. This position DOES NOT require an advanced degree. REQUIREMENTS -2+ years experience as a Medical Writer in a pharmaceutical advertising agency or medical education company -must have very strong Power Point (slide development) experience -strong interactive writing experience (web sites, audio scripts, video scripts, etc) -experience

Requirements: Bachelors Degree in Graphic Design 1 plus years experience in graphic design Must possess knowledge of Quark XPress, Adobe CS3 and strong understanding of design and typographic principles Solid knowledge of the print production process is required Proficient working in a Mac OS X environment required Excellent verbal and written communications skills, attention to detail and the ability to multitask Must work well in a fast paced team environment as well as individually Must be

Job Description: At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical

Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results, not formality

General Office DemandsEntry level experience in technical writing4-year degree or related field or equivalent experienceMust be able to express ideas clearly and logically and love to write. Must be able to create documentation plans and schedules; and drive for deliverables to these schedules. Must have mastery of MS Office Suite including Word, PowerPoint and Excel. Knowledge of Visio, Flash and RoboHelp is a huge plus. Essential skills also include: Writing - Communicating effectively with others in

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

For over 25 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. We have helped over 800 clients to develop and launch some of the most important drugs and

USANA Health Sciences, Inc., a worldwide leader in manufacturing high quality, science-based nutritional supplements, seeks a highly organized individual to coordinate and write distributor profiles for its bi-monthly magazine, which is delivered to more than 100,000 independent USANA distributors throughout North America. A bachelor s degree in journalism, communications, or a related field is required. The successful candidate will possess strong communication and writings skills, an attention to detail

DescriptionThe Director Talent Management, Medical Device & Diagnostic is responsible for supporting and implementing the overall design and development of talent strategies and building the pipeline of current and future leaders within the MDD businesses at Johnson & Johnson. This individual will be accountable for diagnosing talent management needs and designing solutions aligned to the overall Global Talent Management strategy. Be responsible for implementing value added talent management programs and processes

The Senior Copywriter writes content for the North America general market, sewing U.S., Canada and Jamaica. This position requires an experienced (5+ years), versatile senior copywriter, responsible for content from inception through completion. Content needs to be organized, consistent in tone, creative, accurate and without proofreading errors. The senior copywriter provides initial copy, revises it based on editorial review, proofreads projects and follows through to print/web publishing. Content includes

The Copy Manager / Writer creates the development of global creative solutions, in alignment with marketing, sales, corporate, and business objectives to build brand awareness across multiple regions and the United States. Partners closely with subteam of Designer(s) and Marketing Manager(s) on a project-by-project basis to deliver solutions for Creative Director and Brand Director approval. Works closely with teams of multi-disciplinary staff including Designers, Writers, Production, Project management, Marketing

The Design Manager creates the development of global creative solutions, in alignment with marketing, corporate, and business objectives to build brand awareness across multiple regions and the United States. Partners closely with subteam of Writer(s) and Marketing Manager(s) on a project-by-project basis to deliver solutions for Creative Director and Brand Director approval. Works closely with teams of multi-disciplinary staff including Writers, Production, Project management, Marketing, Events, Video, Promotions

Job Description: Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results

Major Duties and Responsibilities: 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 review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Negotiates timeline development for preparation

Novartis Institutes for BioMedical Research is Novartis' global research organization and is committed to discovering innovative medicines that cure disease and improve human health. By conducting more relevant and predictable drug discovery that can yield new and better medicines for patients, Novartis Institutes for BioMedical Research is redefining drug discovery in the post-genomic era. Over the past four years, Novartis Pharmaceuticals has had the greatest number of new molecular entities approved by

R&D Documentation Specialist Barr Pharmaceuticals, Inc. is a global specialty pharmaceutical company engaged in the development, manufacture and marketing of generic and proprietary pharmaceuticals, biopharmaceuticals and active pharmaceutical ingredients. Barr Pharmaceuticals, Inc. is a holding company that operates through its principal subsidiaries: Barr Laboratories, Inc., Duramed Pharmaceuticals, Inc. and Pliva d.d. and its subsidiaries. The Barr Group of companies markets more than 120 generic and 27

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Responsibility for creating and managing the creation of training materials around various processes related to regulatory submissions. Provide some trainings directly. Develop and maintain SOPs and work on special projects as needed. Responsible for archiving health authority submissions and correspondence

Welcome to Novartis - the company that considers its employees to be its greatest asset. Good Business. Great Opportunities. How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Think What's Possible.Responsibility for creating and managing the creation of training materials around various processes related to regulatory submissions. Provide some trainings

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

Job Summary The Publications Group (globally) is accountable for developing leading-edge publication strategies and plans for AstraZeneca products. Ensuring delivery of these plans through a range of outsourcing partners will allow AstraZeneca to gain and sustain competitive advantage. This role will provide: Leadership of the development and delivery of leading-edge publication strategies to support brand differentiation and claims for maximum impact in line with the overall brand communication strategy

Job Title Sr. Medical Writer Location Cambridge,MA Requisition Number RUSABIO291-628595 Job Description Responsible for moderately complex Medical Writing activities in the support of clinical studies. May be responsible for highly complex writing activities, such as additional regulatory support documents or submissions (i.e. INDs, Briefing Books). Participates on SMTs and provides leadership and facilitation (project management) of Medical Writing activities for those teams, including overseeing

Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. Responsibilities: Prepare a variety of documents for clinical regulatory submissions

Job Description: Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results

Job Description: Company Information: Breakthrough Careers! A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results

Responsible for supporting the collection and filing of documents generated for Clinical Trials. C oordinates with the Clinical Project Leader the distribution, retrieval and review of regulatory documents required for initiation of a clinical trial. Assures currency of required clinical trial documents within Central Files (i.e., CVs, FDA 1572, Lab Certification, Financial Disclosure, etc.) throughout the clinical trial. Supporting the staff of the clinical department by answering phones, and processing

As the world's largest healthcare services company with more than $80 billion in annual sales, McKesson Corporation (McKesson) is a Fortune 16 Corporation that provides pharmaceutical supply management and information technologies across the entire continuum of healthcare. This opportunity is within the McKesson Health Solutions which offers a comprehensive suite of care management services to help public and private payers better manage the cost and quality of care. McKesson Health Solutions is one of the

Synta seeks a talented Medical Writer to join our expanding team to collaborate with other bright, motivated professionals to document our clinical trials from conception to registration. Our multiple clinical programs provide exciting science and the opportunity to make varied and meaningful contributions. Responsibilities: - Prepare, edit, and review clinical documents such as study protocols, Investigators' Brochures, and documents for IND applications/ NDAs , as well as abstracts, posters, and articles

Job Number: 06500808 Department: Clinical Development Description: The Medical Writer II/III will be responsible for reviewing and preparing clinical/regulatory documents to support all phases of clinical drug development. As a member of an inter-disciplinary project team, the Medical Writer will review, edit and write study protocols, investigator brochures, regulatory submissions, integrated clinical/statistical reports, and prepare manuscripts for publication. He/she will work closely with internal

Job Summary: Maintain and operate FLI document control systems and databases. Issue, distribute and track documents. Prepare, process, review and/or approve document change requests (DCRs). Assist the Document Control Manager in making improvements in FLI document control systems. Essential Functions: - Providing clerical and administrative support to maintain/operate/review the corporate controlled documentation system. - Assists the Document Control Manager in making improvements in FLI document control

People Depend On Our Products We Depend On Our People. Forest Laboratories is an exciting, growth-oriented prescription pharmaceutical company focused on helping people enjoy healthier, more fulfilling lives. Forest's principal marketed products include Lexapro (escitalopram oxalate) a selective serotonin reuptake inhibitor (SSRI) for the treatment of depression and anxiety; Namenda (memantine HCl) for the treatment of Alzheimer's disease; Benicar (olmesartan medoxomil) an angiotensin receptor blocker

Job Title Sr Medical Writer Location Cambridge,MA Requisition Number RUSABIO275-625395 Job Description Responsible for moderately complex Medical Writing activities in the support of clinical studies. May be responsible for highly complex writing activities, such as additional regulatory support documents or submissions (i.e. INDs, Briefing Books). Participates on SMTs and provides leadership and facilitation (project management) of Medical Writing activities for those teams, including overseeing

Job Title Sr. Medical Writer Location San Diego,CA Requisition Number RUSABIO269-623118 Job Description Responsible for moderately complex Medical Writing activities in the support of clinical studies. May be responsible for highly complex writing activities, such as additional regulatory support documents or submissions (i.e. INDs, Briefing Books). Participates on SMTs and provides leadership and facilitation (project management) of Medical Writing activities for those teams, including overseeing/coordinating