Regulatory Affairs Specialist
- Mexico
- ICON Strategic Solutions
- Regulatory Affairs
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
As a Regulatory Affairs Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
A Regulatory Specialist is a Regulatory professional who contributes to drug development, through provision of regulatory guidance and operational support to early drug development, agency interactions, clinical trial applications, marketing application and post approval support.
Regulatory advice to drug development is key to ensuring our clients pursue first time right strategies to overall product development and to clinical programme development.
You are:
- Scientific (any science discipline)or Pharmacy degree
- Regulatory specialist could come from any ICON department (especially ICO, Clin ops) if you have prior regulatory experience in Agency, CRO or Pharma Industry or from the role of SSUA.
- English fluent ,write & read
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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
.png)
Teaser label
IndustryContent type
BlogsPublish date
01/18/2024
Summary
Introduction to Regulatory Affairs in Clinical Research Regulatory affairs play a pivotal role in ensuring the safety, efficacy, and quality of pharmaceutical products and medical devices. In the
Similar jobs at ICON
Salary
Location
China, Beijing
Location
Beijing
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
TBD
Reference
JR133564
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
Job DescriptionResponsibilities• Lead the setup of the TMF Study processes and Document List (SSDL) • Monitor completeness and quality of TMF content for all assigned clinical trials until study close
Reference
JR135775
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
India, Chennai
Department
Clinical Trial Management
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
We are currently seeking a Senior TMF Specialist to join our diverse and dynamic team. As a Senior TMF Specialist at ICON, you will play a pivotal role in managing the Trial Master File (TMF) for clin
Reference
JR132671
Expiry date
01/01/0001

Author
Kavitha K
Author
Kavitha KSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
We are currently seeking a Senior TMF Lead to join our diverse and dynamic team. As a Senior TMF Lead at ICON, you will play a pivotal role in overseeing the Trial Master File (TMF) management activit
Reference
JR136025
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
We are currently seeking a TMF Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for overseeing the Trial Master File (TMF) management processes, ensuring compl
Reference
JR136023
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Argentina, Buenos Aires
Location
Buenos Aires
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
We are currently seeking a Senior TMF Lead to join our diverse and dynamic team. As a Senior TMF Lead at ICON, you will play a pivotal role in overseeing the Trial Master File (TMF) management activit
Reference
JR136024
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda Obregon