Work From Home during Covid Job Opportunity At Icon Clinical Research

Icon Clinical Research Released Job Openings On 11/01/2022.Icon Clinical Research Limited is an Indian multinational corporation that provides information technology, consulting and business process services. The Fortune India 500 ranks it the 29th largest Indian company by total revenue. It is also ranked the 9th largest employer in India with over 221,000 employees.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Icon Clinical Research Recruitment 2021 are provided below. Interested and eliible candidates can  submit application along with resume. 

Vacancy Details:

Icon Clinical Research Hiring Any Graduates with 05 – 10 Years of Experience for For Senior Medical Writer Position.Complete Details for the Senior Medical Writer as follows..

Important Details :

• Location :Chennai, Bangalore/Bengaluru, Trivandrum/Thiruvananthapuram (WFH during Covid)
• No of Vacancies:04
• Details of Salary: Not Disclosed
• Opening date for online Application: 11/01/2022
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job : QA,QC,R&D,Production,Sales,Packing,RA,Engineering,Medical Coding,Purchase,StoresJobs At Hyderabad,Bangalore,Vizag,Ahmedabad,Mumbai etc 

Job Description/Skills Required

General Medical Writing

• You will write clinical trial reports and other regulatory documents.
• Experience in writing CSRs, Protocols, Investigator Brochures, DSURs, PSURs (safety documents), submission documents.
• You will provide additional writing and editing services as required (e.g. for publications).
• You will advise on the content and format requirements for clinical reports and regulatory documents.

Narrative Writing

• You will write patient narratives for serious adverse events and drop-outs due to non-serious adverse events; write the reports of clinical trials and other regulatory documents (including) according to Icon Clinical Research or client-specified formats.
• You will provide additional writing and editing services (e.g. for publications) as required.
• You will assist in the production of preclinical summaries, clinical summaries, pharmacokineti

Click here for Official notification and Apply