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Medical Writer Jobs

Search all 537 Biotech Jobs for Medical Writer Jobs


Job Title: Medical Writer
Company: The Montco Group
Location: Costa Mesa, CA

Description:
Medical Writer- publication planning Company-Largest West Coast health care agency. Position- Develops scientific publications and presentations including manuscripts for publication in the peer-reviewed literature, abstracts, poster and slide presentations, product monographs, and symposia proceedings. Location- California Therapeutic Areas- Neurology or eye-care preferred. Would consider others. Education- Advanced degree in science or medicine




Job Title: Medical Writer II
Company: MedFocus
Location: Chicago, IL

Description:
IN-HOUSE MEDICAL WRITER COMPANY INFO: MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel. Our client is a global, broad-based health care company devoted to discovering new medicines, new technologies and new ways to manage health and is seeking to add a In-House Medical Writer to their team in Northern Suburb of Chicago, Illinois. RESPONSIBILITIES: - Prepares technical documents to support both domestic and international regulatory submissions. - Incorporates text, graphs, charts, tables and statistical analysis. - Proofreads, circulates, edits, assembles, inspects and duplicates product submissions. - RN to write Serious Adverse Event (SAE) narratives for a large outcome study. QUALIFICATIONS: - 3-5 years exp. - Requires a Clinical Background - Must have good computer skills to prepare and edit narratives. - Excellent clinical background to write complex case narratives. EDUCATION: - RN MedFocus offers competitive wage and benefits packages; Health Insurance, Dental Insurance, long term disability, Holiday and Vacation Time, life insurance and 401K may be applicable.




Job Title: Medical Writer - Oncology
Company: New Horizons Recruiting LLC
Location: Atlanta, GA

Description:
Medical Writer - Oncology Our award-winning Medical Communications Client is seeking an experienced medical writer for their office in Atlanta . You will have the opportunity to join a team that enjoys an excellent rapport with some of the top names in the pharmaceutical & medical device industries. They have enjoyed long-term & sustained growth & are looking for someone to grow with them. Project capabilities of this company include (but are not limited to): CME, Promotional, Publication Plans, Advisory Boards, Faculty Meetings, Grand Rounds, Investigator Meetings, Enduring Materials & Interactive Media/Internet projects. A VERY COMPETITIVE compensation package is available….professional, but casual work environment. To be considered, you must have: 1+ years medical writing experience creating key messages, solid science & excellent readability for projects in a medical communication, pharmaceutical, or pharmaceutical agency environment (some CME experience a plus, but not necessary). Experience writing on the subjects of Oncology is also a plus. Ph.D., Pharm.D or an MD Exceptional team skills Interested parties are welcome to contact Marilyn Sundburg at: Register to View or e-mail Register to View All resumes are held in the strictest confidence. Also, please visit our website (http://www.NewHorizonsRecruiting.com) to view other opportunities & visit our Candidate Resource Room for interesting industry links & information regarding immigration possibilities Key words: Medical Writer, Medical Writing, Pharmaceutical Communications, Scientific Writing, Medical Communications, Publication Planning, Peer-reviewed journal articles, slide kits, monographs, abstracts, CD-ROM, web content e= n >




Job Title: Medical Writer
Company:
Location: Wayne, PA

Description:
Company-Rapidly growing healthcare communications company located in the suburbs of Phila.Position- Medical Writer will prepare manuscripts, abstracts, posters, slide presentations as well as review articles and other clinical documents..  Location- Philadelphia, Pa. suburbsEducation/Experience- Advanced Degree in science or medicine.  Experience writing and publishing scientific articlesTherapeutic area- Preference in vaccines, cardio, or nutraceuticals,  but would consider others. 




Job Title: Medical Writer / Sr. Medical Writer
Company: Ivory Systems
Location: Bloomsbury, NJ

Description:
We are in need of highly skilled Medical Writers for either fulltime or consulting engagements. 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 articles, and abstracts and posters; preparing documents that have high quality scientific content, organization, clarity, accuracy, format and consistency with adherence to guidelines; taking an active role with respect to the planning of content, format, and timing of documents, report scheduling and tracking; providing support to the assigned clinical development team to ensure that project needs and department standards are met, while completing reports within established schedules and timelines; interacting effectively with team leaders, project physicians, statisticians, programmers and regulatory personnel, and facilitating effective interactions and information exchange/communication among co-authors/reviewers as appropriate; keeping abreast of project status, clinical operating plans and ongoing/new studies as well as scientific literature within the assigned area; maintaining/developing knowledge of regulatory guidelines, technological advances, and industry standards, and participating in other tasks as required. BS/BA in biology, nursing or relevant discipline; training in computer applications, GCPs, medical terminology and the drug development process. 4+ years of medical writing experience required. Must be detail oriented, possess excellent writing organizational and communication skills and the ability to work as a member of an integrated team. Experience with electronic publishing of documents an asset. Must be computer literate in MS Windows-based applications. If you are interested in this position, please send a formatted copy of your resume to Register to View




Job Title: Clinical Communications Specialist (Medical Writer) -
Company:
Location: chicago, IL

Description:
Donahoe Purohit Miller is a full-service pharmaceutical advertising agency located in downtown Chicago. We are seeking a dynamic biomedical scientist with an interest in the business of healthcare marketing. As an integral member of the advertising department, you will have the opportunity to play a pivotal role in the continued success of an award-winning company. We offer a broad array of strategic and creative capabilities. The successful candidate will be an enthusiastic, self-motivated person with a strong scientific foundation, will hold an advanced degree (a PhD, MD or PharmD). and possess the ability to communicate complex scientific concepts clearly to a wide variety of audiences, using your experience in writing a full spectrum of promotional materials. You will work with our account teams in the development of strategic concepts, provide direction to copywriters, produce first draft copy for highly technical subjects and ensure the accuracy and completeness of clinical and scientific content. If you enjoy writing and learning about pharmacologic management of disease, have excellent communication and presentations skills and can manage multiple projects with tight deadlines we would love to hear from you. Dermatology, oncology, pharmacology or immunology expertise is preferred. DPM offers an excellent benefits package that includes medical insurance, a 401(k) plan and company paid employee dental and vision coverage, long-term disability and life insurance coverage. Send inquiries, curriculum vitae, and salary requirement to Register to View referring to code #MW1208. Occasional travel required. Clinical experience a plus. Principals only. Recruiters, please don't contact this job poster. Please, no phone calls about this job! Please do not contact job poster about other services, products or commercial interests.




Job Title: Medical Writer - San Bruno
Company: KnowledgePoint360 Group
Location: San Bruno, CA

Description:
We are looking for an experienced Medical Writer to join our staff. Key objectives·         To consistently produce high quality medical education and communications materials for the pharmaceutical industry and other educational bodies that consistently meet the project specification, budget and delivery schedule.·         To maintain an up-to-date knowledge of healthcare compliance guidelines, laws and standard operating procedures and ensure adherence at all times.  Main duties·         Carefully take, correctly interpret and implement a project specification/brief.·         Research, write, edit and proof copy to the highest standard (scientific and grammatical) for a full range of medical education and communications materials including scientific abstracts papers, posters, oral presentations, print items, and multimedia.·           Professional liaison with pharmaceutical industry key contacts, healthcare professionals and other external service providers.·           Accurate/precise interpretation and incorporation of amendments.·         Manage/co-ordinate materials through design/production to print-ready stage, according to standard operating procedures.·         Check printer’s proofs (text, layout, colour, specification) and sign-off for print/production.·         Provide direction for the development of creative designs.·         Develop and implement project schedules.·         Support the delivery of scientific meetings including pre-meeting and on-site activities, preparation of content, liaison with pharmaceutical industry staff, faculty, speakers and audiovisual providers. Skills and knowledge required·         Educated to degree level or above in a biomedical discipline.·         Good understanding of healthcare and the pharmaceutical industry.·         Experience of delivering medical writing projects to specification and service delivery timelines in an agency or comparable environment.·         Excellent scientific writing style and ability to adapt to target audience.·         Attention to detail – style/consistency, grammar, syntax, scientific accuracy, layout and design.·         Excellent project/time management and organisational skills.·         Demonstrate creativity in the production of engaging medical education and communication materials.·         Excellent inter-personal and communication skills.·         IT skills (including Microsoft Office, database and internet searching).·         Understanding and adherence to healthcare compliance laws and guidelines.·         Understanding of print/production procedures.·         Budget and timeline adherence.·         Understanding of drug development process and regulatory guidelines. If you are interested in this position, please send your resume with cover letter, including salary requirements to: Register to View .  EOE.




Job Title: Senior Medical Writer
Company: Adecco Medical & Science
Location: Paramus, NJ

Description:
Adecco Medical & Science has an immediate opening for a Medical Writer for a contract position in New Jersey. Senior Medical Writer with 5 years solid medical writing skills with ISS, PFT and/or NDA experience, for a 3 months assignment (contract). Complete Description: Discuss, develop, produce, revise and/or update protocols and clinical study reports for preclinical and clinical studies. Responsible for developing IB?s, components of IND, Clinical Trial Authorization, NDA submissions, regulatory responses, and other clinical/regulatory documents. Provide support to the assigned clinical development team to ensure clinical/regulatory document development needs and department standards are met, while completing projects within established schedules/timelines. Facilitate conflict resolution across multi-disciplinary teams. Requirements: Experience in the Pharmaceutical industry, Phase l ? ll PK/PD research is is preferred Knowledge of the development, regulatory, quality and compliance environment within the pharmaceutical and marketing environment. Strong interpersonal and communication skills. Familiarity with ICH and AMA guidelines. Proficiency in MS Word, Excel and PowerPoint Please E Mail your resume to [Click Here to Email Your Resumé] or call Thomas now at Register to View Thanks Tom The Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Medical & Science offers benefits including Holiday, 401(k), Insurance Benefit Plans and Anniversary Bonus opportunities. Adecco Medical & Science is an Equal Opportunity Employer.




Job Title: Medical Writer/Communications - Virology
Company: MedFocus
Location: Plainsboro, NJ

Description:
MEDIAL WRITER COMPANY INFO: MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel. Our client is a leading provider of medicines to fight cancer, cardiovascular and infectious diseases -- including HIV/AIDS -- and serious mental illness and is seeking to add a Medical Writer to their team. RESPONSIBILITIES: 1. Develops abstracts, posters, oral presentations and manuscripts 2. Assists internal and external authors in the development of scientific manuscripts for publication in leading peer-reviewed journals 3. Ensures effective planning and management of timelines for all components of assigned documents 4. Works closely with Medical Strategy leads on data displays, document flow, logic and consistency for assigned projects 5. Documents and implements feedback from internal and external authors to determine data interpretation and key findings/messages 6. Develops complex publications according to: a) Good documentation practices (organization, clarity, scientific standards) b) Consistency between text and tabular presentations or graphical displays c) In compliance with PRI documentation standards and external journal requirements d) Alignment with the results of the Clinical Study Report 7. Manages the review process and, on an ongoing basis resolves issues, errors or inconsistencies with pertinent team members to ensure: a) Optimal communication between internal and external authors b) Coordination of consistent and efficient use of medical/scientific language between documents based upon the same data set c) Timely completion and high quality of assigned documents 8) Proofreads and edits documents, as required QUALIFICATIONS: 1. PhD in a science subject or biomedical degree plus medical writing experience 2. Demonstrated strong writing skills as evidenced by good quality writing in publications, in peer-reviewed journals or in pharmaceutical regulatory documentation 3. Analyzed and interpreted complex data from a broad range of scientific disciplines 4. Knowledge of statistics and their application to the interpretation and presentation of clinical data 5. Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills in a cross-functional team 6. Good knowledge of the drug development process (clinical or post-marketing activity); therapeutic area knowledge is a plus 7. Ability to assimilate, interpret and integrate complex clinical data into high-quality publications 8. Good interpersonal skills - able to work well within a publication team 9. Computer skills to include ability to create figures and tables in a Power Point format and Word 10. Knowledge of Cardiovascular/ Metabolics, Oncology, or Virology therapeutic area. 11. Able to work full time and on site 3-4 days a week MedFocus offers competitive wage and benefits packages; Health Insurance, Dental Insurance, long term disability, Holiday and Vacation Time, life insurance and 401K may be applicable.




Job Title: EXPERIENCED MEDICAL WRITERS - great benefits! -
Company:
Location: philadelphia, PA

Description:
Envision Pharma, a stable and growing medical communications company, is seeking full-time, on-site, non-regulatory medical writers to join our team. Our clients are among the top pharmaceutical companies in the world. We have medical communication offices in Philadelphia, PA; Fairfield, CT; San Francisco, CA: and Horsham, United Kingdom (UK). US candidates must be legally eligible to work in US; UK candidates must be eligible to work in the UK. SENIOR WRITERS WILL Work with pharmaceutical clients and key opinion leaders Be involved in publication planning strategy and implementation Ensure your writing and your team`s writing is medically and scientifically accurate and meets client objectives, timelines, and budgets Assign projects and provide direction to medical writers on your team Partner with an Account Manager to coordinate activities with client and internal teams. SENIOR CANDIDATES MUST HAVE THE FOLLOWING BACKGROUND Medical writing experience directed to physicians and specialists Managed and mentored medical writers of varying experience Interacted with client and key opinion leaders/authors Excellent project management skills Full knowledge of the AMA writing style Skilled in publications strategy, planning, and implementation Medical writer, medical director, or team lead experience in a medical writing agency An advanced degree in life science or medically-related field such as PhD in pharmacology or biomedical science, PharmD, or MD. OUR ENVIRONMENT AND BENEFITS Great team-based environment 100% company-paid medical and dental premiums for you and your family. Medical coverage begins your first day of work; dental begins the first of the month following 30 days of service. 100% company paid short- and long-term disability coverage for you Flexible Spending Accounts - health and dependent 401(k) plan with generous company contributions and immediate vesting 24 days off per year + holidays Ongoing training Laptop; you may occasionally telecommute Casual dress Employee referral program HOW TO APPLY To apply, please send your resume, cover letter, and stated areas of therapeutic expertise to: Register to View For more information, please visit our website at www.envisionpharma.com Location: Philadelphia, PA Principals only. Recruiters, please don't contact this job poster. Please, no phone calls about this job! Please do not contact job poster about other services, products or commercial interests.




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