TMF Specialist
- India
- ICON Strategic Solutions
- Clinical Trial Management
Talent Acquisition Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
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
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
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. I have been at ICON since 2013 and I have been growing my career here from the ground up. I star
by
Adrienne Purdy
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Career ProgressionContent type
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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
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Inside ICONContent type
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Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the
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