In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and ...
In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and ...
In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and ...
In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and ...
Drive adoption of TMF SID and enterprise modeling standards. Metadata & Data Asset Management * Lead enterprise metadata management activities. * Oversee the Data Catalog, Business Glossary, Metadata ...
Drive adoption of TMF SID and enterprise modeling standards. Metadata & Data Asset Management * Lead enterprise metadata management activities. * Oversee the Data Catalog, Business Glossary, Metadata ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Maintain TMF health and ensure timely document submission * Develop quality monitoring plans and ... Experience managing global clinical trials and multi-regional teams * Demonstrated experience in ...
Clinical Research Associate, Sponsor Dedicated
$71K - $189K/yr
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
Clinical Research Associate, Sponsor Dedicated
$71K - $189K/yr
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
Clinical Research Associate, Sponsor Dedicated
$71K - $189K/yr
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
Clinical Research Associate, Sponsor Dedicated
$71K - $189K/yr
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
... TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management ...
Clinical Research Associate
Tempe, AZ · On-site
... M/Senior CRM as appropriate. * Verify that essential regulatory documents are collected and filed appropriately in the Trial Master File (TMF) and confirm that the Investigator Site File (ISF) is ...
Quick apply
Clinical Research Associate
Tempe, AZ · On-site
... M/Senior CRM as appropriate. * Verify that essential regulatory documents are collected and filed appropriately in the Trial Master File (TMF) and confirm that the Investigator Site File (ISF) is ...
Clinical Project Coordinator
Tempe, AZ · On-site
... TMF) maintenance and perform study and/or site-level audits to ensure that study files are current, accurate, complete and audit-ready. * Assist with study and site-level management of the Clinical ...
Clinical Project Coordinator
Tempe, AZ · On-site
... TMF) maintenance and perform study and/or site-level audits to ensure that study files are current, accurate, complete and audit-ready. * Assist with study and site-level management of the Clinical ...
Clinical Project Coordinator
Tempe, AZ · On-site
... TMF) maintenance and perform study and/or site-level audits to ensure that study files are current,accurate,completeand audit-ready. * Assistwith study and site-level management of the Clinical Trial ...
Clinical Project Coordinator
Tempe, AZ · On-site
... TMF) maintenance and perform study and/or site-level audits to ensure that study files are current,accurate,completeand audit-ready. * Assistwith study and site-level management of the Clinical Trial ...
Clinical Safety Specialist
Tempe, AZ · On-site
Provide Clinical Safety Management support for BDPI clinical studies to enable successful ... Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that Clinical ...
Clinical Safety Specialist
Tempe, AZ · On-site
Provide Clinical Safety Management support for BDPI clinical studies to enable successful ... Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that Clinical ...
Clinical Safety Specialist
Tempe, AZ · On-site
Provide Clinical Safety Management support for BDPI clinical studies to enable successful ... Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that Clinical ...
Clinical Safety Specialist
Tempe, AZ · On-site
Provide Clinical Safety Management support for BDPI clinical studies to enable successful ... Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that Clinical ...
Clinical Safety Coordinator
Tempe, AZ · On-site
Provide operational support for Clinical Safety management activities for BDPI clinical studies to ... Support Trial Master File (TMF) maintenance for Clinical Safety documentation and perform study and ...
Clinical Safety Coordinator
Tempe, AZ · On-site
Provide operational support for Clinical Safety management activities for BDPI clinical studies to ... Support Trial Master File (TMF) maintenance for Clinical Safety documentation and perform study and ...
Clinical Safety Coordinator
Tempe, AZ · On-site
Provide operational support for Clinical Safety management activities for BDPI clinical studies to ... Support Trial Master File (TMF) maintenance for Clinical Safety documentation and perform study and ...
Clinical Safety Coordinator
Tempe, AZ · On-site
Provide operational support for Clinical Safety management activities for BDPI clinical studies to ... Support Trial Master File (TMF) maintenance for Clinical Safety documentation and perform study and ...
Tmf Manager information
See Arizona salary details
$26.88 - $32.58
4% of jobs
$32.58 - $38.29
6% of jobs
$38.29 - $43.99
7% of jobs
$48.26 is the 25th percentile. Wages below this are outliers.
$43.99 - $49.69
9% of jobs
$49.69 - $55.39
15% of jobs
The median wage is $57.91 / hr.
$55.39 - $61.09
18% of jobs
$65.16 is the 75th percentile. Wages above this are outliers.
$61.09 - $66.80
21% of jobs
$66.80 - $72.50
7% of jobs
$72.50 - $78.20
6% of jobs
$78.20 - $83.90
3% of jobs
$83.90 - $89.60
2% of jobs
$26
$58
$89
How much do tmf manager jobs pay per hour?
What is a TMF Manager?
A TMF (Trial Master File) Manager is responsible for overseeing the management, maintenance, and compliance of clinical trial documentation. They ensure that the TMF is accurate, complete, and inspection-ready in accordance with regulatory requirements, such as ICH-GCP and FDA guidelines. TMF Managers collaborate with clinical teams, quality assurance, and regulatory authorities to support audit and inspection activities. Their role is critical in ensuring data integrity and regulatory compliance throughout the clinical trial lifecycle.
What are the key skills and qualifications needed to thrive as a TMF Manager?
To excel as a TMF Manager (Trial Master File Manager), you need a solid understanding of clinical trial documentation, GCP (Good Clinical Practice) guidelines, and regulatory requirements—typically supported by a degree in life sciences or a related field. Familiarity with electronic TMF (eTMF) systems, document management software, and relevant industry certifications such as RAC or DIA TMF certificates is important. Exceptional attention to detail, organizational skills, and the ability to communicate effectively across cross-functional teams distinguish top TMF Managers. These competencies are essential for ensuring the integrity, completeness, and audit-readiness of clinical trial documentation throughout the study lifecycle.
What are some typical challenges a TMF Manager might face in their role?
TMF Managers often encounter challenges such as ensuring consistent TMF document quality across multiple studies, meeting tight regulatory submission deadlines, and facilitating communication among global project teams. Keeping the TMF up to date and audit-ready requires strong organizational skills and proactive problem-solving, as studies can involve large volumes of documentation and frequent protocol amendments. Effective TMF Managers routinely collaborate with clinical, regulatory, and quality assurance teams to ensure document accuracy and regulatory compliance. Overcoming these challenges is key to maintaining smooth clinical trial operations and supporting successful regulatory inspections.
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For Tmf Manager jobs in Arizona, the most frequently searched job titles are:
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The top searched job categories for Tmf Manager jobs in Arizona are:
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Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote
Phoenix, AZ
Full-time
Re-posted 19 days ago
Job description
Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!
What you will do
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
Conduct study initiation visits (SIVs)
While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
What you will bring to the role
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
5+ years of experience as a Clinical Research Associate
4-year universitydegree OR Nursing Degree
Experience in CNS/Neurology is required; Psychiatry is strongly preferred
Candidates must reside on the West Coast
Willingness to travel regionally required
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986