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- Provide proofreading, copyediting, and fact-checking support across a multitude of branded and unbranded materials, including promotional materials, clinical overviews, disease state reviews, and topics addressing the managed markets landscape
- Provide direction/supervision to other editors (including freelance resources) to manage the editorial process and ensure accuracy and adherence to agreed-upon specifications
- In addition to excellence in spelling, grammar/punctuation/usage, check for sense and consistency in text and formatting; fact-check and edit annotations for text, graphs, charts, and other visual elements per sources
- Obtain permissions from publishers and/or authors as needed
- Complete account-related agency training as needed to assist in electronic submission and referencing
- Manage submission processes for client’s medical/legal/regulatory review
- Create, maintain and distribute client-specific style guides; ensure all pieces conform to AMA and client style
- Bring promotional copy into compliance with FDA regulations, client and other criteria, as needed
- Maintain a high level of productivity with minimal supervision
- Develop dialog and maintain productive working relationships with project managers, copywriters, designers, and account team on content and scheduling issues regarding workflow to achieve project goals; advocate for best editorial practices
- Work closely with writers to resolve content/referencing issues
- Serve as a resource for editorial questions
- Attend project, editorial, and status meetings
- Minimum of a bachelor’s degree
- Minimum of 2 years of experience as a medical editor
- Experience in a pharmaceutical agency or pharmaceutical company
- Ability to interpret scientific data and a working knowledge of medical terminology
- Familiarity with Medical/Legal/Regulatory review committees at pharmaceutical companies
- Well-versed in the American Medical Association Manual of Style
- Natural inclination toward being a stickler for accuracy and perfection with relentless attention to detail
- Proficient use of MS Word, Excel, PowerPoint, and Adobe Acrobat Professional
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Who we are
Salary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Job Categories
Other
Job Type
Permanent
Description
ICON is looking for a Clinical Pricing Analyst to support Global Development Operations, Global Study and Clinical Management Groups and Therapeutic Area Teams by creation of pricing proposals for cli
Reference
2024-110134
Expiry date
01/01/0001
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Salary
Location
Netherlands, Groningen GRQM (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Groningen
Remote Working
Hybrid: Office/Remote
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Facilities & Administratives Services
Clinic
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Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
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JR118367
Expiry date
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Location
India
Department
Clinical Monitoring
Location
India
Remote Working
Remote
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Clinical Monitoring
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Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2024-110031
Expiry date
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