TMF Specialist
- India
- ICON Strategic Solutions
- Clinical Trial Management
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please see similar roles below...
TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment, eTMF maintenance and support eTMF inspection readiness activities
Location : Bangalore/Chennai
EXPERIENCE & SKILLS
- Ability to interact with Clinical and Regulatory team regarding the receipt, analysis, classification and disposition of documents
- Preferred: knowledge of “Essential Documents” Clinical Trial Documentation
- Good verbal and written communication skills (English and local)
- Attention to detail and ability to multi-task
- Strong problem solving, time management, and organizational skills
- Proficient in use of MS office software including Word, Excel, Access, Share Point & Outlook
- Bachelor’s degree in Sciences required
- Preferred: 2 Years’ experience in Pharmaceutical or Contract Research Organization
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
![A picture of Debora Oh](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/img/Oi_Ywfaw1E2c5AjadgdpUA/75/debora-oh-thumbnail.jpg)
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
![](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2023.17000.2380/img/IPH8e3a3NUdY-wjbPxWFOw/75/Adrienne+Purdy.jpg)
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A Day In The LifeContent type
BlogsPublish date
04/21/2023
Summary
From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON? I have been at ICON since 2013 and I have been growing
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Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
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