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Job Description:

Medical Writer I - UK or US

US-Pennsylvania-North Wales; UK-Eastleigh


Reference 057439


Medical Writer I - UK or US This is a rare opportunity to join our friendly global Medical Writing team which sits within ICONs Clinical Research Services group Our remit is to produce high quality documents supporting clinical studies and regulatory submissions

Our key department values are Passionate about partnership
Quality without compromise
Flexibility in a dynamic environment
We have an opening for Medical Writer I based in either the UK or US

In this role you will have the following responsibilities Preparation and QC of imaging documents including Charters, Imaging Manuals and Training Manuals This includes
Working with internal study teams to determine/clarify project requirements and obtaining necessary information
Tracking and recording progress against contracted hours/budget using financial tracking tools and the departments project database Early flagging to management of projects not on track and facilitation of the Change Order process
Attendance at internal and external projects meetings via teleconference/Webex
Writing of documents according to agreed contractual obligations and timelines using client or ICON templates and style guides, and adhering to regulatory or other guidance
Incorporation of review comments from internal and external reviewers, including management of multiple sets of comments
Perform QC of documents written by other writers
To keep Medical Writing senior management informed of project status and any issues that affect document quality, timelines, and adherence to contractual obligations
Achievement of individual utilization (billability) target
Compliance with department systems, eg, project database, timesheets, training
General operational assistance to the Medical Writing team
Preparation and QC of other document types, if required
Active participation in department initiatives and process improvements
Any other task deemed reasonable by department senior management

Skills & experience required Bachelors degree in a life science, or equivalent
Previous experience as a clinical/regulatory Medical Writer
Able to assimilate and summarize large volumes of scientific data accurately, clearly and concisely
Proficiency in MS Word, Excel, PowerPoint, Adobe Acrobat and Outlook Able to rapidly learn to use bespoke in-house and client toolbars
Excellent verbal English
Excellent written English, eg, organization, syntax, grammar, clarity, focus, messaging that requires minimal editing/rewriting
Excellent attention to detail

Preferred Knowledge of imaging techniques such as CT, MRI, PET, Echo, X-ray, DxCT
Experience of working for a large CRO
Familiarity with Veeva Vault, Salesforce and Box

Competencies Able to recognize, exemplify and promote ICONs OwnIt culture and values of Accountability and Delivery, Integrity, Collaboration and Partnership
Proactive, gracious and collaborative communication skills
Able to work in a fast-paced, results-driven environment
Culturally aware and able to work comfortably within a global team

Benefits of Working in ICON Other than working with a phenomenal team of passionate and ambitious people, we also offer a very competitive benefits package This varies from country to country so a dedicated recruiter will discuss this with you at interview stage

We care about our people as they are the key to our success We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career

Whats Next

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity

Would you like to find out more before applying If so, please contact one of our Talent Acquisition Specialists who will be very happy to speak with you

ICON is an equal opportunity employer M/F/D/V and committed to providing a workplace free of any discrimination or harassment

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Healthcare, Biotechnology/Pharmaceutical/Medicine
Functional Area : HR/PM/IR/Training
Role : Recruitment
Salary : As per Industry Standards
Deadline : 18th Feb 2020

Key Skills:

Company Profile:


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