Lead TMF
- Mexico
- Clinical Trial Support
- ICON Strategic Solutions (FSP)
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
As a Lead TMF Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
You will be joining one of our global pharmaceutical clients; a prestigious organization, specializing in a niche rare disease, complemented by a pipeline in other therapeutic areas, including oncology. A company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership.
What you will be doing:
- The role independently maintains the Trial Master Files for assigned studies, participating in end-to-end TMF management activities, including adherence to organizational TMF standards and study-level quality control reviews, and facilitating issue resolution.
- Ensure TMF completeness and accuracy based client´s SOPs and regulatory requirements
- Maintain study-level TMFs including QC review, analysis, and vendor oversight (if applicable)
- Conduct content review of a variety of documents in a short time frame while maintaining consistency and attention to detail
- Prioritize work accordingly to meet departmental needs and work toward and meet deadlines with some supervision
- Generate metrics for department and study team usage supporting TMF completeness, timeliness and quality
- Participate in inspection readiness reviews, preparation activity and inspection conduct
- Provide guidance and training as applicable to TMF stakeholders; serve as a resource to colleagues on more advanced TMF activities
- Coordinate onboarding of new staff
- Participate in and may lead projects that require cross-functional collaboration or involve coordinating system updates
You are:
- Bachelors degree in relevant discipline
- Strong verbal/written communication, presentation skills and interpersonal skills to educate/train project teams and other stakeholders and exchange key information
- Effectively communicates and coordinates activities within the group and other TMF stakeholders
- MS Excel, Word, PowerPoint expertise
- Experience working in a TMF platform
- Experience working in a CTMS platform
- Possess strong critical thinking skills with a focus on inspection readiness
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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
Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
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
Teaser label
Inside ICONContent type
BlogsPublish date
05/22/2022
Summary
Having enjoyed steady growth over the last several years, it’s predicted that the global clinical trials market will hit a value of $65.2 billion by 2025, and around 58% of this can be attribute
Teaser label
Inside ICONContent type
BlogsPublish date
08/26/2020
Summary
Wearable technology has become a normal part of everyday life, from fitness trackers and smart watches to smart jewellery and implantables, more sophisticated wearable medical devices are reachi
Similar jobs at ICON
Salary
Location
Chile, Santiago
Location
Santiago
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of opera
Reference
JR153588
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Bulgaria, Sofia
Location
Sofia
Remote Working
Hybrid
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.What You Will Do:You will take o
Reference
JR153364
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
Bulgaria, Sofia
Department
Real World Solutions
Location
Sofia
Warsaw
Barcelona
Madrid
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Site Management Associate II with Dutch language to join our diverse and dynamic team. As a Site Management Associate II at ICON, you will play a vital role in supporting th
Reference
JR153858
Expiry date
01/01/0001
Author
Teodora KaykievaAuthor
Teodora KaykievaSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a SMA II at ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelin
Reference
JR153698
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Site Management Associate II at ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical P
Reference
JR153591
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Japan, Osaka
Location
Osaka
Tokyo
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Trial Assistant (CTA) to join our diverse and dynamic team. As a Senior CTA at ICON Plc, you will play a key role in supporting the management and execution
Reference
JR145743
Expiry date
01/01/0001