- 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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BlogsPublish date
10/08/2025
Summary
A Career Built on Purpose: Dimitar's Journey at ICON Plc Dimitar Karzhin’s career path is not one he could have predicted. What began with a decade as a practicing General Practitioner in Bulgaria l
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09/19/2025
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How to Build a Strong LinkedIn Profile That Attracts Employers LinkedIn is no longer just a digital CV. It is a professional network, a space to showcase your skills and a platform to connect with
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BlogsPublish date
09/16/2025
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Growing with ICON: Christina’s Journey in Clinical Operations and Quality Leadership At ICON, we are proud to showcase the incredible journeys of our colleagues who make a real impact on pati
Salary
Location
Romania, Bucharest
Location
Sofia
Warsaw
Bucharest
Remote Working
Office or Home
Job Categories
Contracts Administration
Job Type
Permanent
Description
Role Summary:Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with investigative sites.Responsibilit
Reference
JR135054
Expiry date
01/01/0001
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Salary
Location
Bulgaria, Sofia
Department
Clinical Monitoring
Real World Solutions
Location
Sofia
Remote Working
Office or Home
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinic
Reference
JR136939
Expiry date
01/01/0001
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Salary
Location
Romania, Bucharest
Department
Clinical Monitoring
Real World Solutions
Location
Bucharest
Remote Working
Office or Home
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinic
Reference
JR136927
Expiry date
01/01/0001
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Salary
Location
India, Chennai
Location
Chennai
Trivandrum
Remote Working
Office Based
Job Categories
Accounting & Finance
Job Type
Permanent
Description
Accounts Receivable Associate (Billing)Location : Chennai / TrivandrumWe are currently seeking an Accounts Receivable Associate (Billing) to join our diverse and dynamic team. The Accounts Receivable
Reference
JR136576
Expiry date
01/01/0001
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Salary
Location
Hungary, Budapest
Location
Budapest
Remote Working
Remote
Job Categories
Corporate Support
Job Type
Permanent
Description
We are currently seeking a Contract Analyst I to join our diverse and dynamic team. As a Contract Analyst I at ICON, you will play a pivotal role in preparing, verifying, and carrying out invoicing vi
Reference
JR136874
Expiry date
01/01/0001
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Salary
Location
UK, Reading
Department
Real World Solutions
Location
Reading
Remote Working
Office or Home
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Late Phase Senior Clinical Research Associate to join our diverse and dynamic team within ICON's late phase group known as ICO. As a Senior CRA within this division you can
Reference
JR134410
Expiry date
01/01/0001
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