Lead TMF
- Mexico
- Clinical Trial Support
- ICON Strategic Solutions
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
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials a
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
Similar jobs at ICON
Salary
Location
Australia, Sydney
Department
Clinical Monitoring
Real World Solutions
Location
Sydney
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and managem
Reference
JR135029
Expiry date
01/01/0001
Author
Joanne ShinAuthor
Joanne ShinSalary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Job Advert PostingAs a SMA I, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.JOB PURPOSESite Management Associate is r
Reference
JR136816
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara DrozdowskaSalary
Location
Bulgaria, Sofia
Location
Sofia
Bucharest
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking candidates with a global study management experience to join our diverse and dynamic team.We are looking for candidates who have experience in global study management supporti
Reference
JR136508
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
US, Long Beach, CA
Department
Accellacare Site Network
Location
Los Angeles
Long Beach
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site net
Reference
JR136206
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
Romania, Bucharest
Department
Real World Solutions
Location
Warsaw
Bucharest
Barcelona
Madrid
Gdansk
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Site Management Associate to join our diverse and dynamic team. As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site manage
Reference
JR134304
Expiry date
01/01/0001
Author
Teodora KaykievaAuthor
Teodora KaykievaSalary
Location
Australia, Sydney
Location
Sydney
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis
Reference
JR137097
Expiry date
01/01/0001
Author
Krisztina AuthAuthor
Krisztina Auth