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- Researches assigned projects comprehensively (conducts literature searches using tools such as MEDLINE, Ovid, R&D Insight, obtains reprints of articles, reads background material, including books, journal articles, study reports, etc.)
-
Writes in a clear and concise manner, incorporating the following basic writing elements:
- Good grammar, punctuation, vocabulary, and spelling
- Use of appropriate scientific terminology
- Good sentence flow; sentences are organized in a coherent and ordered manner
- Information is presented in a logical, organized, scientific manner
- Writing is scientific, not conversational, and appropriate for the target audience
- Ensures referencing is appropriate and correct
- Chooses appropriate, timely references
- Chooses the appropriate data from source
- Cites data appropriately and accurately in text
- Uses primary references preferentially; understands appropriate use of secondary references
- Incorporates messages in a scientifically appropriate manner
- Demonstrates good attention to detail
- Writes specific projects as assigned within the budgetary constraints of the proposal and project plan.
- Asks relevant client queries that are appropriate in tone and quality
- Establishes and maintains good relationships and direct communications with clients and authors on project-specific tasks
- Responsible for assisting and working with creative and editorial support staff to provide necessary background and technical information required to complete tasks and for review and approval of work
- Responsible for attendance, as required, at project meetings and for providing status reports at these meetings regarding projects in progress
- Attends off-site meetings with client as required
- Demonstrates a clear understanding of scientific data, statistical methods and commonly encountered study designs
- Demonstrates proficiency in software required for scientific writing and presentations, including SharePoint, PowerPoint, Word, Adobe Acrobat, etc.
- Responsible for familiarization with AMA and Company styles of writing
- Accurately and completely incorporates client, comments as appropriate
- Uses version control appropriately
- Incorporates all changes, and resolves conflicting instructions/revisions
- Responsible for fact checking (including references) and spell checking all manuscripts and project materials before submission to senior staff
- Accurately highlights appropriate parts of references and submits copies of all highlighted references with all projects
- Advanced degree in a life science (PharmD, MD, PhD)
- Minimum of 3 years of related experience and/or training
- Solid knowledge of the managed markets, payer, market access and/or pharmacoeconomics space
- Experience with clinical and scientific information
- A self-starter with exceptional writing and research skills, a good command of AMA style, superb time-management skills, and a solid knowledge of communications styles
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Who we are
Salary
Location
United States
Department
Biometrics Roles
Location
United States
Remote Working
Remote
Job Categories
Clinical Data Management
Clinical Data Scientist Lead
Clinical Systems
Data Standards Consultant
Job Type
Permanent
Description
As a Project Data Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2024-110193
Expiry date
01/01/0001
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Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid: Office/Remote
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Description
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JR118865
Expiry date
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Location
US, Raleigh, NC
Department
Full Service - Corporate Support
Location
Raleigh
Remote Working
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Job Type
Intern
Description
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Regional United States (PRA)
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Location
US, Blue Bell (ICON)
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Blue Bell
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Description
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Expiry date
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Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
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Expiry date
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