Not Synergistech’s Jobs

Job Requisition: 21537

The Company
Few organizations can keep up with the fast-paced, 24/7 nature of today’s media coverage; even fewer can claim to have helped shape it. Bloomberg has long been a leading source of data and news and presents one of the most challenging environments in financial journalism. Bloomberg offers a unique opportunity to produce real-time stories that shape the markets and our world.

The Role
Bloomberg News seeks a Health and Science Editor to join its Health, Science, and Education team. The person in this role will help shepherd coverage of major drug-makers, device makers, biotechnology companies, insurers, pharmacy benefit managers, public health issues, health-care policy, and medical science. Knowledge of the economy, financial markets, and business is essential. A minimum of three years of business editing experience at a major newspaper or wire service is preferred. The successful applicant will produce breaking news stories under real-time deadline pressure, ensuring they are clear, comprehensive, and accurate.

The successful applicant is expected to have the proven ability to make snap decisions about stories that regularly appear on TOP, Bloomberg’s front page. The editor will also be expected to serve as a mentor and coach to reporters and be comfortable working within a team environment.

Qualifications

• Bachelor’s degree or equivalent experience
• Experience covering major drug-makers, device makers, biotechnology companies, insurers, pharmacy benefit managers, public health issues, health-care policy, and medical science
• Proven success in business, financial, and economics reporting
• Ability to write clear, concise, and accurate news stories
• Ability to write quickly under pressure of real-time deadlines

To apply:
https://bloomberg.taleo.net/servlets/CareerSection?art_ip_action=FlowDispatcher&flowTypeNo=13&pageSeq=2&reqNo=54221&art_servlet_language=en&selected_language=en&csNo=10000

Req Number 26820BR
Location Parnassus Avenue
Department Name Dean’s Office, School of Medicine, Student Affairs
Work Days M-F, 8-5

Job Summary
The Senior Editor will write, edit and oversee the design and production of medical student-related websites, calendar of events and publications; write letters of recommendation to support student applications for post-graduate training, scholarships, awards and non-research fellowships and programs; assist Office of Student Affairs with planning and implementation of Orientation, Senior Convocation, Commencement and Advisory College events, including production of written material and programs to support these events; and perform other duties as assigned.

Required Qualifications
BA/BS in English, journalism or an allied field, or in a subject matter area related to the editorial specialty, demonstrated editing and writing abilities, and at least two full years of professional editorial experience; or an equivalent combination of education and experience; excellent writing and editorial skills; working knowledge and experience with the following software programs: Outlook, Word, InDesign and Dreamweaver.

Preferred Qualifications
Photoshop skills/experience.

To apply:
https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?SID=^_slp_rhc_EiR84gwY_slp_rhc_AyyNPEKlPnimHwok/dz9IWFKX2wJMpf8xD6t_slp_rhc_4XWROoQQ3huMg2Bi0fAyscUC6/kXL_C_R__L_F__slp_rhc_BrKfStfp/K1l0oPUZ28s66w1I/Cppc=&jobId=863629&type=search&JobReqLang=1&recordstart=1&JobSiteId=5226&JobSiteInfo=863629_5226&GQId=0

Req Number 26284BR
Location Mission Bay
Department Name Pharmaceutical Chemistry; Mass Spectrometry

Job Summary
Molecular and Cellular Proteomics, published by American Society of Biochemistry and Molecular Biology is seeking an experienced Editorial Assistant to support the offices of the Co-Editors at UCSF. Incumbent will manage the manuscript peer review process, which includes ensuring the timely processing of submitted manuscripts, assessing compliance with journal rules and guidelines; facilitate manuscript reviews through the journal editors, associate editors & reviewers, & track all steps & correspondence; coordinate/perform other journal activities and programs; take meeting minutes for Associate Editor Meetings and manage action items so generated; perform other duties as assigned.

Required Qualifications
Graduation from college with work in English, journalism, or an allied field, or in a subject matter area related to the editorial specialty, and demonstrated editing and writing abilities, and at least two full years of professional editorial experience; or an equivalent combination of education and experience; science background with a BA or higher; excellent written and verbal communication skills; computer skills; detail oriented; ability to meet tight deadlines.

Preferred Qualifications
3-5 years experience; previous experience with electronic tracking system (preferably Bench Press)

To apply:
https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?SID=^_slp_rhc_EiR84gwY_slp_rhc_AyyNPEKlPnimHwok/dz9IWFKX2wJMpf8xD6t_slp_rhc_4XWROoQQ3huMg2Bi0fAyscUC6/kXL_C_R__L_F__slp_rhc_BrKfStfp/K1l0oPUZ28s66w1I/Cppc=&jobId=845665&type=search&JobReqLang=1&recordstart=1&JobSiteId=5226&JobSiteInfo=845665_5226&GQId=0

Job ID: 0124

Alexza Pharmaceuticals is a specialty pharmaceutical company located in Palo Alto, California. We are developing breakthrough therapies for the treatment of acute and intermittent medical conditions. Alexza was founded by Dr. Alejandro Zaffaroni who is one of the most successful entrepreneurs in the biomedical industry with a long list of successful start-ups to his credit, including ALZA, Affymax and Affymetrix Corporations.

We have an exciting opportunity for a Medical Writer. This person will work closely with our multi-disciplinary team of scientists and engineers who are dedicated to the development of novel drug delivery technologies with the potential to revolutionize the treatment of several common diseases.

Responsibilities:

• Writes manuscripts for publication based on clinical study reports, published literature, and other sources as required.
• Prepares draft abstracts and posters for submission to/presentations at scientific meetings.
• Serves as author of clinical sections of a large volume of regulatory and clinical documents (e.g., study reports) supporting clinical trials and product approvals, working independently with minimal direction, while ensuring appropriate and effective collaboration with key functional contributors.
• Acts as an internal consultant to R&D functional groups on the content and optimal presentation of regulatory documents to facilitate achievement of submission objectives and in accordance with regulatory document requirements / guidance.
• Assists with the development of Company training programs with respect to regulatory submission requirements and related processes. Spearheads group initiatives in relation to document standards, continuing MS template development, cross-functional processes and other aspects of document management (in collaboration with publishing group). Participates in other highly complex Company-wide initiatives

Skills required:

• Excellent medical writing and verbal communication skills
• Knowledgeable of document management, authoring and publishing tools and their applicability for workflow efficiency
• Knowledge of global regulatory affairs and particularly the requirements and mechanisms for regulatory approval in the United States and Europe
• Must be organized, have the ability to successfully manage multiple projects, be able to work in a team environment, and communicate effectively in a fast-paced setting

Education and experience:

• Requires a BS or BA with 5+ years of relevant experience in a medical writing/clinical submissions environment directing/preparing documents for regulatory submissions
• Demonstrated experience in the preparation of regulatory documents

We offer competitive compensation and benefits including stock options, an exciting and collaborative work environment and excellent opportunity for career growth.

To apply:
http://recruit.trovix.com/jobhostmaster/jobhost/ViewJobPostDetails.do?title=MEDICAL+WRITER&jobPostId=raaqhlst7zfjlbq5w6cakjuyye&accountId=7c53a637038448c994213f5421f85cb853453e77&button=&action=viewDetails

Job Code: 08-1000021671

Responsibilities:
This position is responsible for the writing, editing, and assistance in submitting clinical manuscripts for peer-reviewed journals, as well as abstracts, posters, and presentations for medical congress. This individual will also be responsible for the timely delivery of publications outlined in product-specific publication plans. The timely publication of clinical trial manuscripts directly impacts Genentech’s strategic imperatives and is critical to the achievement of its corporate goals.

Job Qualifications:
Candidates must possess a graduate-level degree (PhD, MD, RN, PharmD) in the life sciences (immunology, cell biology e.g.). Candidates must also possess a minimum of 3-5 years medical writing and editing experience with clinical trial manuscripts and posters for the biotechnology and/or pharmaceutical industry. This individual must effectively and clearly communicate across multiple functional areas with a diverse group of scientists, statisticians, marketing managers, and other team members, and manage multiple projects working independently as well as within functional teams. The senior writer must work with minimal supervision to complete their projects. Candidates will also have demonstrated ability to set priorities and work within tight deadlines without compromising publication quality. This individual must have good organizational and interpersonal skills and demonstrate attention to detail.

Candidates must possess advanced Microsoft Word skills. Working knowledge of Endnote and Powerpoint and some familiarity with graphics programs a plus.

To apply:
http://www.linkedin.com/jobs?viewJob=&jobId=511341&fromSearch=21&sik=1209353860504

Job Title Sr Writer, Technical
Company Applied Biosystems
Location Foster City, CA
Requisition 08-21615
Job Function Marketing Communications

As the leading supplier of life science technology and related applications, we are helping life scientists understand and use the power of biology to pursue new scientific discoveries and methods for diagnosing and treating disease. If you’re interested in a challenging career in one of the fastest moving fields today, you’ve come to the right place.

Major Responsibilities:

• Write and revise documentation needed to support a consumables manufacturing organization.
• Working with Development and R&D staff, prepare Bills of Material, work instructions, QC protocols, and validation procedures required for the release of new products.
• Review all new documentation to assure accuracy, clarity, and standardization.
• Format documents to Company standards, and release documentation to Corporate document control.
• Support projects to review and revise older legacy procedures, SOPs, work instructions and calculation sheets.
• Revise documents to correct issues raised by Discrepancy Reports or audit nonconformances.
• Work with Department staff to revise and upgrade training materials and records.
• Support site-to-site technology transfer by revising and formatting documentation to meet site requirements.

Requirements:

• Min 3-5 years of experience as a technical writer for hardware/software products or life science industry.
• Excellent writing, editing and communications skills with a strong design sense.
• Solid experience with MS Office environment, including editing features.
• Education: Min A.S. degree or Technical certificate in Technical Writing, English or Communications or related discipline. B.S. in a Life Science discipline a plus.

To apply:
http://www.resumeware.net/applera_rw/applera_web/resume_new_web.cfm?rType=External&reqnum=8267&from=website&include_rb=0

Job Title Technical Writer II
Company Applied Biosystems
Location Foster City, CA
Requisition 08-21474
Job Function Marketing Marketing Communications

Required Responsibilities:

• Write and edit copy (ads, brochures, etc.) for Global Marketing staff
• Write and edit articles for TechNotes & Innovations newsletter
• Cross edit copy from other writers in group
• Edit other scientific materials destined for customers
• Participate in ongoing product training and R&D lab meetings
• Maintain project tracking docs, style docs, newsletter tracking docs, as needed.

Minimum Education/Experience Requirements:

• Master’s degree (M. A.) or equivalent in molecular biology, biochemistry or similar field; or 4-10 years related experience and/or training; or equivalent combination of higher education and experience.
• 2+ years laboratory research

Preferable Skills and Attributes:

• excellent written & verbal communication skills
• strong scientific background in DNA sequencing, genotyping, and PCR (especially real-time PCR) technologies
• advanced use of MSWord (editing features), Excel, PowrPoint, and Adobe Acrobat for editing pdfs; knowledge of FrameMaker and Quark/InDesign a plus
• aptitude for learning new software
• ability to get along with a broad range of personalities; strong people management skills
• analytical, thorough, detail oriented,independent, high level of initiative, with good organizational skills
• ability to multi-task and prioritize in order to meet deadlines
• strong project management skills
• adaptable to the changes that occur in a high growth environment

To apply:
http://www.resumeware.net/applera_rw/applera_web/resume_new_web.cfm?rType=External&reqnum=8196&from=website&include_rb=0

Requisition Number: 07-0091
Post Date: 7/31/2007
Title: Medical Writer
City: Novato

BioMarin Pharmaceutical develops and commercializes innovative biopharmaceuticals for serious diseases and medical conditions, focusing on product candidates that:

• Address currently unmet medical needs (the “orphaned diseases”, including genetic ones
• Suggest a clear-cut development profile
• Provide an opportunity to be first-to-maket.

SUMMARY DESCRIPTION

The Medical Writer participates as a member of clinical teams, serves as team specialist in clinical documentation, and drafts and edits documents needed to support clinical research studies.

RESPONSIBILITIES

In collaboration with key contributors, writes, edits, and formats clinical regulatory documents (principally protocols, informed consent forms, and clinical study reports) that conform to global regulatory submission and internal document standards. Assists in the development and maintenance of document templates and guidelines that conform to document specifications and internal publishing requirements for regulatory filing. Assists in development and update of SOPs for developing regulatory documents for clinical research.

EDUCATION

Requires a BS or higher degree in a scientific discipline. Evidence of professional development in medical writing or editing (such as AMWA or BELS certification) preferred. Evidence of professional development in the area of regulatory documentation (classes, workshops, or certification) preferred.

EXPERIENCE

A minimum of one to three years of experience writing documentation for clinical trials for a pharmaceutical, biotechnology, or contract research company, or university medical center. Requires a BS or higher degree in a scientific discipline and a minimum of 2 years experience with a BS, at least 1 year of experience with an MS or higher degree, and demonstrated working knowledge of scientific principles.

Skills:

• Must have excellent writing, editing, and oral communication skills.
• Familiarity with clinical regulatory documentation requirements.
• Ability to research and review clinical content effectively and translate information into clear and concise messages using AMA style in the English language.
• Ability to successfully organize and manage multiple simultaneous projects from conception to completion, working collaboratively in a team environment; to communicate effectively in a fast-paced setting; and to re-prioritize writing tasks quickly.
• Proficiency in Word, Powerpoint, and Excel, and familiarity with document management software (eg, Documentum or Livelink)

To apply:
https://www.ultirecruit.com/bio1001/jobboard/CanLogin.aspx?__JobID=*E06D9956873F0202&__RT=*2121BF73EBC1EF25B67FA995E21A6E9BACA95A9A2724AC61608FE054DFA4E05AC2BFB754C55FD045

Department: Clinical Research

Description:

Primary responsibility is to write, edit and review clinical documents for submission to regulatory agencies, eg, FDA, according to ICH guidelines.

Duties and Responsibilities:

• Participate as a member of cross-functional teams to write, edit, and review clinical/regulatory documents, including study protocols and amendments, clinical study reports. Investigator Brochures, integrated safety and efficacy summaries, clinical portions of FDA briefing documents, and other documents that support IND/NDA/eCTD applications.
• Develops and manages timelines of writing projects from inception through final signature.
• Establishes and maintains document standards, styles, and formats according to ICH guidelines.
• Reviews and edits documents for compliance, consistency, clarity, and accurate use of scientific terminology; facilitates discussion in the case of conflicting interpretations.
• Interacts with clinical, preclinical, biometry, regulatory, and scientific staff to obtain analytical information and data necessary to complete documents and projects.
• May collaborate with medical writing consultants on specific writing projects, eg, clinical study reports, to facilitate collection of data and study information, routing of reviews, and finalization and approval of the document.
• May also edit or write abstracts, manuscripts, slide and poster presentations, and investigator newsletters, as needed.
• Other duties may be assigned.

Job Requirements:

• Master’s or Ph.D. in a biological or biomedical science (eg, Biology, Immunology, Chemistry, Pharmacology, or Nursing). A master’s degree in English or journalism, with additional science and technical or medical writing coursework may be acceptable in lieu of a science degree.
• Minimum of 5 years of medical writing experience in a regulated environment (eg, pharmaceutical or biotechnology company, contract research organization), or university medical center, hospital, or research institute. A bachelor’s degree in a scientific discipline may be acceptable with a minimum of 8 years of medical writing experience.
• Experience in preparation of clinical/regulatory documents for U.S. regulatory submissions; experience with ex-U.S. regulatory documents is a plus.
• Excellent interpersonal, organizational, and communication skills; detail oriented.
• Ability to manage and prioritize multiple ongoing projects from conception to completion, and work in a team environment.
• Ability to work with little or no instruction on routine work and general instructions on new assignments.
• Understand good clinical practices (GCPs) and relevant ICH guidelines, specifically those governing the creation and submission of clinical study reports, protocols, Investigator’s Brochures, and other clinical/regulatory documents such as the Common Technical Department.
• Ability to analyze and synthesize date from a broad range of disciplines; produce clearly written scientific documents.
• Proficiency with Microsoft® Office Applications, particularly MS Word, Excel, PowerPoint, and Outlook.
• Ability to prepare graphic presentations of data using Excel, Visio, or other graphic software is a plus.

Anesiva is an equal employment opportunity employer and promotes diversity throughout its workforce. Applications and resumes are considered for all positions without regard to race, color, religion, sex, national origin, ancestry, age, medical condition, physical or mental disability, marital status, sexual orientation, or veteran status.

To apply:
http://www.anesiva.com/wt/page/current_opportunities/job/1214_001/apply

Job ID               0124
Job Location      Mountain View

Job Category     Clinical

Alexza Pharmaceuticals is a specialty pharmaceutical company located in Palo Alto, California. We are developing breakthrough therapies for the treatment of acute and intermittent medical conditions. Alexza was founded by Dr. Alejandro Zaffaroni who is one of the most successful entrepreneurs in the biomedical industry with a long list of successful start-ups to his credit, including ALZA, Affymax and Affymetrix Corporations.

We have an exciting opportunity for a Medical Writer. This person will work closely with our multi-disciplinary team of scientists and engineers who are dedicated to the development of novel drug delivery technologies with the potential to revolutionize the treatment of several common diseases.

Responsibilities:

• Writes manuscripts for publication based on clinical study reports, published literature, and other sources as required.
• Prepares draft abstracts and posters for submission to/presentations at scientific meetings.
• Serves as author of clinical sections of a large volume of regulatory and clinical documents (e.g., study reports) supporting clinical trials and product approvals, working independently with minimal direction, while ensuring appropriate and effective collaboration with key functional contributors.
• Acts as an internal consultant to R&D functional groups on the content and optimal presentation of regulatory documents to facilitate achievement of submission objectives and in accordance with regulatory document requirements / guidance.
• Assists with the development of Company training programs with respect to regulatory submission requirements and related processes. Spearheads group initiatives in relation to document standards, continuing MS template development, cross-functional processes and other aspects of document management (in collaboration with publishing group). Participates in other highly complex Company-wide initiatives

Skills required:

• Excellent medical writing and verbal communication skills
• Knowledgeable of document management, authoring and publishing tools and their applicability for workflow efficiency
• Knowledge of global regulatory affairs and particularly the requirements and mechanisms for regulatory approval in the United States and Europe
• Must be organized, have the ability to successfully manage multiple projects, be able to work in a team environment, and communicate effectively in a fast-paced setting

Education and experience:

• Requires a BS or BA with 5+ years of relevant experience in a medical writing/clinical submissions environment directing/preparing documents for regulatory submissions
• Demonstrated experience in the preparation of regulatory documents
• We offer competitive compensation and benefits including stock options, an exciting and collaborative work environment and excellent opportunity for career growth.

Alexza Pharmaceuticals is an Equal Opportunity Employer.

To apply:
http://www.alexza.com/careers/open.php