Associate Writer Jobs
By University of Iowa At Iowa, United States
Typically six months of collective technical writing experience through coursework and work experience.
Ability to format documents using the Microsoft suite of software, including the use of Word in a Microsoft operating system.
Demonstrated success in editing/formatting/writing of technical documents associated with the field of biotechnology or a related field of commerce.
Evidence of a personal interest in technology.
Appointment Type: Professional and Scientific
Work Modality Options: Hybrid within Iowa
Associate Writer Jobs
By University of Iowa At Iowa City, IA, United States
Typically six months of collective technical writing experience through coursework and work experience.
Ability to format documents using the Microsoft suite of software, including the use of Word in a Microsoft operating system.
Demonstrated success in editing/formatting/writing of technical documents associated with the field of biotechnology or a related field of commerce.
Evidence of a personal interest in technology.
Appointment Type: Professional and Scientific
Work Modality Options: Hybrid within Iowa
Senior Medical Writer- Associate Scientific Director
By GLE Talent At Ann Arbor, MI, United States
"Great work environment, friendly team, good on-site hours with the opportunity to work from home."
Maintain up-to-date knowledge of and adhere to GPP2, PhRMA, FDA (including FDAAA), and OIG guidelines
(doctorate-level) with 3+ years of agency experience in medical writing
Knowledge of therapeutic areas, science, and products for all assigned accounts
Ability to simultaneously manage numerous, complex projects with overlapping timeframes, deadlines
Strong interpersonal communication, organizational, and problem-solving skills
Associate Medical Writer Jobs
By Randstad USA At Illinois, United States
Developing knowledge of current electronic document management systems and information technology.
Understands, assimilates, and interprets sources of information with appropriate guidance/direction from development teams and Medical Writing mentor/management.
Developing knowledge of US and international regulations, requirements and guidance associated with document preparation and submissions.
Learning US and international regulations, requirements and guidance associated with document.
Developing knowledge with Common Technical Document (CTD) content templates.
Excellent written and oral communication skills.
Associate Writer Jobs
By Series AI At Seattle, WA, United States
Strong collaboration skills & ability to self-manage when we need to divide & conquer
Proven experience in a writer or equivalent role, with a strong portfolio of work.
Experience in mobile game design is a plus.
Comprehensive knowledge of the mobile gaming market and the standout aspects of successful interactive stories is a plus.
Work with the Head of Story and the story team to author outlines & scripts that bring our vision to life
Review and provide feedback on scripts, character designs, and storyboards.
Associate Medical Writer Jobs
By Merck At Boston, MA, United States
Candidates must have demonstrated presentation, writing, and project management skills
Learns to interpret data and apply knowledge of basic regulatory/compliance/scientific requirements to document preparation
Develops knowledge of regulatory medical writing and therapeutic area/investigational product to support pipeline projects
Candidates must have experience working on teams
Prepares selected components of regulatory clinical documentation
Participates, with supervision, on document-specific teams
Associate Medical Writer Jobs
By NaturalIndustryJobs.com - Natural and Organic Industry Jobs At United States
Or bachelor's level scientist with 2-3 years’ experience in medical communications, medical/clinical lab or pharmaceutical environment
Computer technology experience and the ability to learn systems quickly and effectively; demonstrated experience using virtual communications (Zoom, Teams, etc.)
Experience with Microsoft Office (Outlook, Word, Teamwork, PowerPoint, and Excel)
Excellent organizational skills, ability to prioritize multiple objectives/duties and strong attention to detail
Strong interpersonal and listening skills; the ability to communicate (verbal/writing) effectively at all levels and with all customers, internally and externally
Draft and edit scientific publications including abstracts, posters, and manuscripts in partnership with our data scientists for submission to peer-reviewed publications
Associate Medical Writer Jobs
By PRECISIONvalue At New York, NY, United States
1 year of experience in the medical communication, pharmaceutical and/or healthcare industry.
Knowledge of American Medical Association (AMA) style.
You are driven and excited by the challenge to learn and grow
You are naturally curious, a life-long learner with a strong interest in healthcare and writing.
You are flexible, able to handle multiple projects at once and do your best work in an energizing environment
Degree focus in Writing, English, Life Sciences or related field.
Associate Medical Writer Jobs
By PRECISIONvalue At New York, United States
1 year of experience in the medical communication, pharmaceutical and/or healthcare marketing agency industry
Knowledge of American Medical Association (AMA) style.
You are driven and excited by the challenge to learn and grow
You are naturally curious, a life-long learner with a strong interest in healthcare and writing.
You are flexible, able to handle multiple projects at once and do your best work in an energizing environment
Degree focus in Writing, English, Life Sciences or related field.
Associate Medical Writer Jobs
By OPEN Health At Parsippany, NJ, United States
Have a strong scientific background and good basic writing skills
Strong scientific background (preferably PhD) and some experience with written scientific communications
Aptitude for the English language and excellent written and verbal communication skills
Ability to perform all duties remotely and online, as OPEN Health is a paperless company
Ability to manage multiple competing priorities
Proficiency with MS Office programs (Word, Excel, PowerPoint, Outlook) and PubMed searching. EndNote experience is a plus!
Medical Writer Jobs
By Exactech At Gainesville, FL, United States
Functional/Technical Knowledge, Skills and Abilities Required:
Develop and support risk/benefit analyses.
Independently manage multiple medium to large scale writing/research projects.
Providing knowledge and support to the company's different business units to enable operation within company and regulatory guidelines.
Experience in systematic literature review required
Experience in medical devices preferred
Medical Writer Jobs
By Intelliswift Software At New York, United States

Qualifications: Education: Bachelor's degree or above in a scientific field. • Min 2 years medical writing experience; previous work experience in a global medical information group, preferred. ...

Medical Writer Jobs
By eJAmerica At Mounds View, MN, United States
Good To Have- EU MDR Knowledge
· Minimum of 2 years experience in medical technology quality/regulatory field, proofreading, technical editing or related field.
• Comply with assigned and scheduled training requirements
Must to have: MS Office, Adobe acrobat/reader
• Review and approve labeling in Medtronic’s quality system.
• Interface with the Cardiac Surgery business unit leads to determine work needs and priorities
Medical Writer Jobs
By Intelliswift Software At Pennsylvania, United States

Qualifications: Education: Bachelor's degree or above in a scientific field. • Min 2 years medical writing experience; previous work experience in a global medical information group, preferred. • ...

Medical Writer Jobs
By Kyverna Therapeutics At Emeryville, CA, United States
Extensive knowledge of drug development process (phase I-IV clinical trials), GCP, CFR, and ICH regulatory requirements and guidelines.
Manage protocol amendment process, including authoring and review
Experience with preparation of clinical protocols, study reports, IND, IB, NDA/CTD documents or peer-reviewed publications desirable.
Expert knowledge of US and international guidance and regulations associated with scientific publications.
Ability to manage medical writing for multiple programs with competing timelines and priorities.
Working knowledge of statistical concepts and techniques
Medical Writer Jobs
By Astrix At United States

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking ...

Medical Writer (Pmcf) Jobs
By Select Source International At United States

Seeking candidates who are knowledgeable with EU-MDR regulations and experienced medical writers of regulatory documents like the PMCF plans and reports.

Medical Writer - (Inds)
By BioSpace At San Francisco, CA, United States
Ability to thrive in a fast-paced research environment and highly skilled in multitasking, time management, delegation, and prioritization.
Title and salary will be commensurate with education and experience.
Coordinating with administrative and research assistants and managers to coordinate operations.
2 years experience authoring IND applications (preferably CBER)
Experience authoring toxicology and/or manufacturing sections of IND (preferably for antivirals)
Knowledge of a variety of administrative operational activities.
Medical Writer 2 Jobs
By BioSpace At New York, NY, United States
Demonstrated excellent presentation, communication, and project management skills.
Interpret data and apply knowledge of regulatory/compliance/scientific requirements to document preparation.
Independently manage document lifecycle, including timeline management, review cycle management, and document quality management where appropriate.
Contribute to document development as an independent lead author and as part of a larger team.
Help to iteratively improve medical writing processes as appropriate.
Demonstrated scientific or medical writing acumen.
Medical Writer I Jobs
By ICON plc At Blue, AZ, United States
Minimum of 1-3 years’ experience of high-level content development
Applicants with prior relevant experience in a medical publications/medical communications agency preferred
Representing assigned work at internal and external (client) meetings as required (e.g., project status, author interactions, client publication committee meetings, etc)
Background research and writing support for new business proposals
Background research and writing support for assigned account(s) organic growth opportunities
Advanced degree, preferably PhD but PharmD and MD may also be considered

Are you looking for an exciting opportunity to join a leading medical communications agency as an Associate Medical Writer? We are looking for a talented individual to join our team and help create compelling content for our clients. You will be responsible for researching, writing, and editing scientific and medical content for a variety of projects. If you have a passion for medical writing and are looking to make a difference in the healthcare industry, this is the perfect job for you!

Overview An Associate Medical Writer is a professional who is responsible for 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 medical journal articles. They must ensure that all documents are accurate, up-to-date, and meet the standards of the relevant regulatory bodies. Detailed Job Description An Associate Medical Writer is responsible for researching, writing, and editing medical documents. They must ensure that all documents are accurate, up-to-date, and meet the standards of the relevant regulatory bodies. They must have a strong understanding of medical terminology and be able to write in a clear and concise manner. They must also be able to work independently and as part of a team.

What is Associate Medical Writer Responsibilities?

• Researching and writing medical documents such as clinical trial protocols, patient information leaflets, and medical journal articles
• Ensuring accuracy and up-to-date information in all documents
• Meeting the standards of the relevant regulatory bodies
• Working independently and as part of a team
• Maintaining a high level of accuracy and attention to detail
• Keeping up to date with the latest developments in the medical field
Job Skills Required
• Excellent writing and editing skills
• Strong understanding of medical terminology
• Ability to work independently and as part of a team
• Attention to detail
• Ability to work under pressure and meet deadlines
• Knowledge of relevant regulatory bodies
Job Qualifications
• Bachelor’s degree in a related field such as medicine, biology, or life sciences
• Previous experience in medical writing or editing
• Knowledge of relevant regulatory bodies
Job Knowledge
• Knowledge of medical terminology
• Knowledge of relevant regulatory bodies
• Knowledge of medical writing and editing
Job Experience
• Previous experience in medical writing or editing
• Experience working with regulatory bodies
Job Responsibilities
• Researching and writing medical documents
• Ensuring accuracy and up-to-date information in all documents
• Meeting the standards of the relevant regulatory bodies
• Working independently and as part of a team
• Maintaining a high level of accuracy and attention to detail
• Keeping up to date with the latest developments in the medical field