Medical and Scientific Writer/ start up
- Employer
- Labcorp
- Location
- Maidenhead, United Kingdom
- Salary
- Competitive
- Start date
- 12 Apr 2021
- Closing date
- 15 Apr 2021
View more
- Discipline
- Medical Communications, Medical Writing
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Study Level Informed Consent Developer
COVANCE by labcorp
Covance by labcorp have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. But we are much more than a normal CRO:
- We are also the world´s biggest Central Lab, generating more clinical trial data than all other central laboratories combined
- Our Early Phase Solutions have proved to shave off 30 % time from lead candidate to Proof of Concept
- LabCorp/Covance were the first in receiving FDA approval to perform COVID19 tests using an at-home collection kit.
Join us and see why Covance by labcorp are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.
THE JOB
We are looking to recruit apermanent, full time medical/scientific document developer who would primarily be responsible to develop study level Informed Consent Documents and other study level patient facing documents on our studies.
This job offers excellent professional exposure to projects in multiple therapeutic areas, client interface and work dynamics to deliver documents to be used by patients globally. It is a real opportunity for career progression in a growing global Start-up Service Department.
IS THIS YOU?
As an essential member of the team, the ICF Developer is responsible for development of study level Informed Consent Forms in our clinical trials. The ICF developer work closely with project lead, medical colleagues, document reviewers and the client to maintain quality and deliver study milestones.
- You relish working in a fast-paced environment, on complex and demanding protocols, enabling you to develop your scientific knowledge and writing skills.
- You enjoy working in a friendly and collaborative global ICF developer team environment under a supportive line manager.
- You will expand the scope of your expertise within departmental and cross-departmental capabilities and will be able to work on ICF development as well as sponsor expertise.
APPLY NOW
Unique job with critical study-level documents, client exposure and work dynamics to engage a professional with a scientific mind and a patient centric attitude.
Education/Qualifications:
- University life science degree.
- English native speaker, English bilingual speaker or super proficiency in written English language
- Relevant ICF development, patient document development or other scientific/medical writing experience.
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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