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Medical Writer Consultant Jobs

Medical Writer Jobs
By Medasource At New York City Metropolitan Area, United States
Excellent oral and written communication, presentation, conflict management and problem-solving skills are required.
Experience in pharmaceutical content creation to promote engagement and education.
Collaborate with the clinical content team to develop a gamification and monetization strategy that enhances user experience and promotes behavioral change.
Provide industry-relevant experience and expertise to scientific programs.
Deep understanding of customer-centric experience design approaches and methodologies, including design thinking, usability testing, etc.
Content, including but not limited to practice exercises, user quests and games, and reward feedback loops.
Medical Writer, Medical Information
By Thermo Fisher Scientific At ,
Good knowledge of document management systems and other relevant applications (e.g. Word, Excel, Outlook).
May represent Medical Writing in bid defenses and capabilities presentations.
Bachelor's degree in a scientific field or equivalent and relevant formal academic/vocational qualification.
Experience working in the pharmaceutical/CRO industry preferred.
Solid medical writing skills, including grammatical, editorial, and proofreading skills.
Good knowledge of regulatory documentation and drug development process.
Medical Consultant Jobs
By The Triana Group, Inc. At United States
Perceived benefits and potential challenges related to the technologies we introduce
Review brief demos and provide feedback through online evaluation forms
Brief phone conversations to discuss your evaluations when needed
Hosting a Lunch & Learn session, if interested and feasible on your premises (optional)
Opportunity to join more in-depth studies, tests and other (optional)
Users and their current clinical methods
Medical Writer Jobs
By Profiles, Inc At , Seattle, 98102
Proficiency in Microsoft Office, Adobe Acrobat, reference management software (e.g. EndNote) and research databases (e.g. PubMed).
Working knowledge of the AMA Manual of Style.
Conduct literature searches and developing content that outlines a story arc with a complete annotated reference list.
Support the team in the medical/legal/regulatory (MLR) review process and interacting with the MLR review committee.
New job opportunities are listed daily – www.careerprofiles.com.
Regulatory Medical Writer Jobs
By GForce Life Sciences At United States
Ability to work in a fast-paced environment with effective use of prioritization, organization, and time management skills.
Converts relevant product data and information into a form that is clear, complete, accurate, and meets submission requirements.
Working knowledge of in vitro diagnostic regulation (IVDR)
Minimum of 3-5 years of experience in medical device regulatory affairs, US or international.
Experience writing IVDR technical file documents
Demonstrated organizational skills necessary to support cross-functional product submission preparation.
Medical Writer Jobs
By Agilent Technologies Inc. At , Remote $96,000 - $177,000 a year
Technical Documentation and SAE management for Clinical Trials
Strong knowledge of GCP and FDA regulations.
Excellent writing, communication, and presentation skills.
Strong interpersonal skills with the ability to interact effectively with multiple levels of within an organization.
Writing Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746
Clinical Research, including Systematic Literature Searches and reviews
Medical Writer Jobs
By 7West Communications At , Fort Worth, Tx
Detail orientation, with ability to manage numerous projects simultaneously; excellent time-management skills
Education: B.A. in English, Journalism or B.S. in healthcare-related field; advanced degree a plus
Work Experience: 3 years in healthcare communications
Expert writing, editing and proofreading skills, including solid spelling and grammar
Extensive knowledge of medical and pharmaceutical terminology
Must be familiar with, and adhere to, generally accepted writing and publication standards, as well as individual journal requirements
Medical Writer Jobs
By Brio Group At North Carolina, United States
Develop and maintain templates for study-specific documents, adhering to client and regulatory requirements
Ensure compliance with relevant QSDs, regulatory requirements, and client specifications for the organizations Essential Documents
2+ years of experience within the pharma/biotech/CRO industry working with clinical data and documentation
Serve as a primary or secondary contact for clients, sponsors, and other functional areas within assigned medical writing tasks
Analyze and summarize data from clinical studies and review scientific literature for medical writing tasks
Compose, edit, and evaluate Essential Documents (i.e. CSRs, protocols, safety narratives) and project-specific clinical materials
Medical Writer - Dynamedex
By EBSCO Information Services At Ipswich, MA, United States
Collaborate with a team of highly experienced colleagues and mentors who will help you hone your skills.
Strive for continuous improvements in knowledge and critical thinking
Technical capacity to learn new systems to edit and manage content
Identify, summarize, and organize information from clinical studies, literature reviews, and guidelines from professional medical organizations.
Bachelor’s degree in a related field (Advanced degree preferred)
Interest in science/medicine with desire to learn and work as part of collaborative team
Medical Writer Jobs
By MedThink At ,
Work in a cross-functional team, establishing effective working interactions with editorial, presentation services, account services, and project management teams
Proficiency in Microsoft Word, PowerPoint, Excel, Outlook, and reference management software (e.g., Endnote, Reference Manager)
1-year postdoctoral research or prior scientific communications agency experience with developing publications, including scientific manuscripts for peer-reviewed journals
Excellent writing and problem-solving skills
Prior experience with developing publications, including scientific manuscripts for peer-reviewed journals
Function within 1 to 3 business units and produce quality products efficiently under multiple timelines
Scientist Medical Writer Jobs
By Cardinal Health At , $36.10 - $51.50 an hour
Experience in clinical or research-based oncology is preferred
Strong technical and mechanical writing skills
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Communicate medical/technical information to targeted audiences (e.g., pharma, provider, general population)
Create data-driven content (slide decks, discussion guides, etc.) for live and virtual events
Attend live and virtual meetings to ensure the successful execution of content strategies created by the Scientific Communications and Strategy team.
Medical Writer Jobs
By Agilent Technologies At California, United States
Technical Documentation and SAE management for Clinical Trials
Strong knowledge of GCP and FDA regulations.
Excellent writing, communication, and presentation skills.
Strong interpersonal skills with the ability to interact effectively with multiple levels of within an organization.
Writing Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746
Clinical Research, including Systematic Literature Searches and reviews
Medical Writer Jobs
By Synectics Inc. At Waukegan, IL, United States
Previous experience working with regulatory submission documents
Previous experience in summarizing scientific studies
Experience in leading cross-functional teams to incorporate feedback into study reports and/or regulatory submission documents
Creating new or updating existing regulatory submission documents.
Excellent ability to learn new software applications
Medical Writer, Cer Jobs
By EG Life Sciences At United States
Experience in writing Clinical Evaluation Reports (CER) per MEDDEV 2.7.1 Rev 4
Experience in Medical Device, specifically class III
Experience in researching clinical articles, documentation and reports.
Experience in reviewing and interpreting clinical data.
Experience in writing risk assessments and clinical data assessments.
Degree or background in a clinical field is a plus (BSN, PhD, etc.)
Medical Writer Jobs
By Getinge At Wayne, NJ, United States
1-5 year’s medical writing experience.
Direct experience working on clinical evaluations within the Medical Device industry a plus.
Medical writing certification a plus.
Health, Dental, and Vision insurance benefits
Short and Long Term Disability Benefits
Job Responsibilities And Essential Duties
Medical Writer Jobs
By MedThink SciCom At Cary, NC, United States
Proficiency in Microsoft Word, PowerPoint, Excel, Outlook, and reference management software (eg, Endnote, Reference Manager)
Work in a cross-functional team, establishing effective working interactions with editorial, graphics, account services, and product management teams
≥1-year postdoctoral research or prior scientific communications agency experience with developing publications including scientific manuscripts for peer-reviewed journals
Excellent writing and problem-solving skills
PhD in life sciences, PharmD
Demonstrable interest in medical writing (eg, participation in other writing initiatives such as scientific blogs, freelancing)
Medical Writer Jobs
By Lumicity At Dallas, TX, United States
Strong organizational skills and ability to manage competing priorities
Minimum of 2 years of industry regulatory writing experience
Excellent communication skills in English (written and spoken)
Previous experience with IND and NDA submissions preferred
Strong interpersonal and teamwork skills
Plan, write, edit, and format clinical development documents
Medical Writer Jobs
By Recruits Lab (We're hiring) At New York, NY, United States
Strong attention to detail, organizational skills, and ability to manage multiple projects simultaneously.
Advanced degree and 3-5 years' experience required
Manage multiple writing projects simultaneously, adhering to timelines and budgets.
Minimum of 3-5 years of experience in medical writing for the pharmaceutical, biotech, or medical device industry.
Excellent written and verbal communication skills, with an ability to communicate complex scientific and medical concepts to various audiences.
Experience with digital pathology or a related field.
Medical Writer - Wfh
By Sarah Cannon At Tennessee, United States
Responsibility for medical writing document version control for study documents created by Medical Writing department, as applicable
Perform literature searches/reviews as necessary to obtain background information and training for development of clinical documents.
Serve as the primary Sponsor contact for clinical document writing on an assigned project
Ensure medical editing review of draft and final documents before external distribution. This includes both copyediting and content review.
It’s More Than a Career, It’s a Mission.
About Sarah Cannon Research Institute
Medical Writer Consultant Jobs
By SAGE Therapeutics At , Remote
Experience, Education and Specialized Knowledge and Skills
Keep management informed on progress documents and other project related information.
Assist management in projecting resources and perform administrative duties as requested.
Working knowledge of ICH and US regulatory requirements is required; working knowledge of other ex-US regulatory requirements is desired.
Documented excellence in advanced features of Microsoft Word and ability to work effectively with a document management system.
Working knowledge of drug development, clinical research, study design, biostatistics, pharmacokinetics, the regulatory environment, and medical terminology.

Are you looking for a rewarding career as a Medical Writer Consultant? Join our team and help us create compelling medical content that will make a difference in the lives of patients!

Overview:

Medical Writer Consultants are professionals who specialize in creating and editing medical documents for a variety of purposes. They are responsible for researching, writing, and editing medical documents such as clinical trial protocols, patient information leaflets, and regulatory documents. They must have a thorough understanding of medical terminology and be able to communicate complex medical information in a clear and concise manner.

Detailed Job Description:

Medical Writer Consultants are responsible for researching, writing, and editing medical documents. They must be able to interpret complex medical information and communicate it in a clear and concise manner. They must be able to work independently and as part of a team. They must be able to manage multiple projects and meet tight deadlines. They must be able to work with a variety of stakeholders, including medical professionals, regulatory bodies, and pharmaceutical companies.

What is Medical Writer Consultant Job Skills Required?

• Excellent written and verbal communication skills
• Ability to interpret complex medical information
• Ability to work independently and as part of a team
• Ability to manage multiple projects and meet tight deadlines
• Knowledge of medical terminology
• Knowledge of regulatory requirements
• Knowledge of pharmaceutical industry
• Proficiency in Microsoft Office

What is Medical Writer Consultant Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in medical writing
• Certification in medical writing (preferred)

What is Medical Writer Consultant Job Knowledge?

• Knowledge of medical terminology
• Knowledge of regulatory requirements
• Knowledge of pharmaceutical industry

What is Medical Writer Consultant Job Experience?

• At least two years of experience in medical writing

What is Medical Writer Consultant Job Responsibilities?

• Researching, writing, and editing medical documents
• Interpreting complex medical information
• Communicating medical information in a clear and concise manner
• Working independently and as part of a team
• Managing multiple projects and meeting tight deadlines
• Working with a variety of stakeholders, including medical professionals, regulatory bodies, and pharmaceutical companies