Lionbridge Life Sciences - search for Clinical Trial experienced translators and reviewers - https://partners.lionbridge.com/: Job 00007256
Source language(s): English
Target language(s): Vietnamese
Details of the project: Dear colleague,
My name is Estelle Martin and I am the Global Vendor Manager for Life Sciences at Lionbridge (www.lionbridge.com).
You are experienced in translating the below Clinical Trial documents:
- Protocol
- Informed Consent Form (ICF)
- Patient Information Leaflets (PIL)
- Patient Information Sheet (PIS)
- Investigator’s brochure (IB)
- Case Report Form (CRF)
- Clinical Study Report (CSR)
Please contact us according to the below scenarii:
1. You have never worked for Lionbridge:
Apply via https://partners.lionbridge.com/ > “Partner Application”.
Evidence your translation/review experience for above type of documents (detailed experience, wordcounts, project descriptions, bilingual file samples, ...).
Enter the keyword “Candidate_for_Clinical_Trial_Projects_and_more” wherever you want under under your profile, our team will find your application quicker that way.
IMPORTANT: We probably will not be able to respond to all emails in a short turn-around time so we plan to prioritize candidates who have created their candidate profile under https://partners.lionbridge.com/. We will invite the others to create their profile.
2. You work for Lionbridge:
Please send an email to your usual contact within Lionbridge Vendor Management team and propose your services for Clinical Trial projects specifically by evidencing your translation/review experience for above type of documents (detailed experience, wordcounts, project descriptions, bilingual file samples, ...).
Please let me know in case you face difficulties,
Thank you.
Best Regards,
Estelle Martin
Life Sciences Global Vendor Manager
Lionbridge
Special requirements to the applicants: You are a native speaker of the target language.
You are experienced in translating the below Clinical Trial documents and can provide evidences of it:
- Protocol
- Informed Consent Form (ICF)
- Patient Information Leaflets (PIL)
- Patient Information Sheet (PIS)
- Investigator’s brochure (IB)
- Case Report Form (CRF)
- Clinical Study Report (CSR)
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