Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that ...
Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that ...
Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that ...
Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that ...
Business Analyst Veeva Vault Clinical (CTMS/eTMF) Work location : Remote Duration: Full Time * Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or ...
Business Analyst Veeva Vault Clinical (CTMS/eTMF) Work location : Remote Duration: Full Time * Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or ...
Manager, TMF Systems and Operations
$109K - $174K/yr
PTO
This position is responsible for supporting CTMS and eTMF activities, executing operational processes, and assisting with system enhancements and training initiatives. Here's What You'll Be Doing:
Manager, TMF Systems and Operations
$109K - $174K/yr
PTO
This position is responsible for supporting CTMS and eTMF activities, executing operational processes, and assisting with system enhancements and training initiatives. Here's What You'll Be Doing:
Associate, TMF Operations
San Diego, CA · On-site
$70K - $100K/yr
Review eTMF quality metrics generated internally or from vendors. * Ensure Vendor Issues Tracker is kept up to date. * Manage Site Master List by overseeing site number assignment process.
Quick apply
Associate, TMF Operations
San Diego, CA · On-site
$70K - $100K/yr
Review eTMF quality metrics generated internally or from vendors. * Ensure Vendor Issues Tracker is kept up to date. * Manage Site Master List by overseeing site number assignment process.
Manager, TMF Systems and Operations
Cambridge, MA · On-site
$109K - $174K/yr
PTO
This position is responsible for supporting CTMS and eTMF activities, executing operational processes, and assisting with system enhancements and training initiatives. Here's What You'll Be Doing:
Manager, TMF Systems and Operations
Cambridge, MA · On-site
$109K - $174K/yr
PTO
This position is responsible for supporting CTMS and eTMF activities, executing operational processes, and assisting with system enhancements and training initiatives. Here's What You'll Be Doing:
eTrial Master File Senior Analyst
Lawrenceville, NJ · On-site
$122K - $122K/yr
Work closely with Global Trial Managers and TMF Study Leads to support the completeness of the TMF • Key deliverables include: ensuring accuracy at the document level in the eTMF for all Client ...
eTrial Master File Senior Analyst
Lawrenceville, NJ · On-site
$122K - $122K/yr
Work closely with Global Trial Managers and TMF Study Leads to support the completeness of the TMF • Key deliverables include: ensuring accuracy at the document level in the eTMF for all Client ...
eTMF Specialist, Pharma, BiAnnual Review Project
Almont, CO · On-site
$65 - $75/hr
Medical
Dental
Vision
Life
Retirement
Remote Our client is seeking an eTMF Specialist to support a biannual review of Phase III Trial Master Files. The specialist will ensure TMFs are complete, accurate, compliant, and inspection-ready ...
eTMF Specialist, Pharma, BiAnnual Review Project
Almont, CO · On-site
$65 - $75/hr
Medical
Dental
Vision
Life
Retirement
Remote Our client is seeking an eTMF Specialist to support a biannual review of Phase III Trial Master Files. The specialist will ensure TMFs are complete, accurate, compliant, and inspection-ready ...
Clinical Trial Associate
Palo Alto, CA · On-site
$39.50 - $53.75/hr
Ensures accurate and timely documentation, including eTMF management, study contractsand financial records in compliance with ICH-GCP, company policies and regulatoryrequirements * Coordinates ...
New
Clinical Trial Associate
Palo Alto, CA · On-site
$39.50 - $53.75/hr
Ensures accurate and timely documentation, including eTMF management, study contractsand financial records in compliance with ICH-GCP, company policies and regulatoryrequirements * Coordinates ...
New
Executive Director, Head of Clinical Operations Excellence
Medical
Dental
Vision
Life
Retirement
PTO
Compliance and eTMF: * Develop, implement, and maintain the GCO Compliance Management Plan, including eTMF. Oversee the relationship with CQA to support and ensure compliance with GCP, SOP and ...
Executive Director, Head of Clinical Operations Excellence
Medical
Dental
Vision
Life
Retirement
PTO
Compliance and eTMF: * Develop, implement, and maintain the GCO Compliance Management Plan, including eTMF. Oversee the relationship with CQA to support and ensure compliance with GCP, SOP and ...
Associate, TMF Operations
San Diego, CA · On-site
$70K - $100K/yr
Review eTMF quality metrics generated internally or from vendors. * Ensure Vendor Issues Tracker is kept up to date. * Manage Site Master List by overseeing site number assignment process.
Associate, TMF Operations
San Diego, CA · On-site
$70K - $100K/yr
Review eTMF quality metrics generated internally or from vendors. * Ensure Vendor Issues Tracker is kept up to date. * Manage Site Master List by overseeing site number assignment process.
Complete activities to confirm study and site-level eTMF completeness and document quality * Set-up and maintenance of study-specific Regulatory Trackers as needed (in lieu of an electronic tracking ...
Quick apply
Complete activities to confirm study and site-level eTMF completeness and document quality * Set-up and maintenance of study-specific Regulatory Trackers as needed (in lieu of an electronic tracking ...
Sr. Clinical Trial Associate
Princeton, NJ · On-site
$35 - $48/hr
Ensure the eTMF is being maintained up-to-date and all essential documents areappropriately filed in the eTMF * Collaborates with CROs to ensure accurate data collection and entry into the CTMS ...
Sr. Clinical Trial Associate
Princeton, NJ · On-site
$35 - $48/hr
Ensure the eTMF is being maintained up-to-date and all essential documents areappropriately filed in the eTMF * Collaborates with CROs to ensure accurate data collection and entry into the CTMS ...
Document and Clinical Systems Manager (TMF)
Medical
Dental
Vision
Retirement
PTO
Lead monthly eTMF meetings for internal CO Study Team * Manages the Clinical System, including managing user access, user training, and system releases * Act as lead Clinical System Admin (add ...
Document and Clinical Systems Manager (TMF)
Medical
Dental
Vision
Retirement
PTO
Lead monthly eTMF meetings for internal CO Study Team * Manages the Clinical System, including managing user access, user training, and system releases * Act as lead Clinical System Admin (add ...
Clinical Trial Assistant
$75K - $90K/yr
Maintain, organize and QC Trial Master Files (TMF/eTMF) to ensure inspection readiness at all times * Assist with study start-up activities, including collection and tracking of regulatory documents ...
Clinical Trial Assistant
$75K - $90K/yr
Maintain, organize and QC Trial Master Files (TMF/eTMF) to ensure inspection readiness at all times * Assist with study start-up activities, including collection and tracking of regulatory documents ...
Clinical Trial Assistant
Foster City, CA · On-site
Maintain, organize and QC Trial Master Files (TMF/eTMF) to ensure inspection readiness at all times * Assist with study start-up activities, including collection and tracking of regulatory documents ...
Clinical Trial Assistant
Foster City, CA · On-site
Maintain, organize and QC Trial Master Files (TMF/eTMF) to ensure inspection readiness at all times * Assist with study start-up activities, including collection and tracking of regulatory documents ...
Sr. Product Specialist
Foster City, CA · On-site
Knowledge on other Vault like Vault eTMF, Vault Promomats etc is good to have but not mandatory. Experience in Veeva SDK Code development ( Good to Have) Excellent communication kills Ability to work ...
Sr. Product Specialist
Foster City, CA · On-site
Knowledge on other Vault like Vault eTMF, Vault Promomats etc is good to have but not mandatory. Experience in Veeva SDK Code development ( Good to Have) Excellent communication kills Ability to work ...
Document and Clinical Systems Manager (TMF)
San Diego, CA · On-site
Medical
Dental
Vision
Retirement
PTO
Lead monthly eTMF meetings for internal CO Study Team * Manages the Clinical System, including managing user access, user training, and system releases * Act as lead Clinical System Admin (add ...
Document and Clinical Systems Manager (TMF)
San Diego, CA · On-site
Medical
Dental
Vision
Retirement
PTO
Lead monthly eTMF meetings for internal CO Study Team * Manages the Clinical System, including managing user access, user training, and system releases * Act as lead Clinical System Admin (add ...
Clinical Trial Associate
$75K - $140K/yr
Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews). * Update and maintain internal ...
Clinical Trial Associate
$75K - $140K/yr
Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews). * Update and maintain internal ...
Senior Clinical Systems Manager
Plainsboro, NJ · On-site
$260K/yr
Medical
Dental
Vision
Retirement
Support study-specific eTMF oversight activities in collaboration with eTMF Oversight teams, including documentation planning, completeness and quality review, inspection readiness, and issue ...
Senior Clinical Systems Manager
Plainsboro, NJ · On-site
$260K/yr
Medical
Dental
Vision
Retirement
Support study-specific eTMF oversight activities in collaboration with eTMF Oversight teams, including documentation planning, completeness and quality review, inspection readiness, and issue ...
Etmf information
See salary details
$34.5K - $43.2K
2% of jobs
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11% of jobs
$85.7K is the 25th percentile. Wages below this are outliers.
$78.1K - $86.9K
9% of jobs
The median wage is $94.1K / yr.
$86.9K - $95.6K
28% of jobs
$95.6K - $104.3K
20% of jobs
$104.6K is the 75th percentile. Wages above this are outliers.
$104.3K - $113K
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9% of jobs
$34.5K
$96.2K
$130.5K
How much do etmf jobs pay per year?
What are the typical daily responsibilities of an eTMF specialist?
As an eTMF Specialist, your daily responsibilities include managing, organizing, and maintaining essential clinical trial documents within the electronic Trial Master File system. You will monitor document completeness, track filing timelines, and ensure regulatory compliance, often collaborating with clinical, regulatory, and quality assurance teams. Regular audits, resolving document discrepancies, and training other team members on eTMF processes are also common tasks. The role requires staying up to date with changing regulatory requirements and maintaining clear communication with multiple stakeholders to support successful clinical trial operations.
What is an eTMF?
An eTMF (electronic Trial Master File) job involves managing and maintaining digital documentation related to clinical trials. Professionals in this role ensure regulatory compliance, organize essential trial documents, and support inspection readiness. They may use eTMF systems to track, classify, and archive trial-related files. Strong attention to detail and knowledge of clinical research regulations are essential.
What are the key skills and qualifications needed to thrive in the eTMF position, and why are they important?
To thrive as an eTMF (electronic Trial Master File) Specialist, you need a strong understanding of clinical trial documentation, regulatory requirements, and document management best practices, often supported by a degree in life sciences or a related field. Familiarity with eTMF systems such as Veeva Vault or Medidata, as well as relevant certifications like the DIA TMF Certificate, is highly beneficial. Attention to detail, excellent organizational skills, and effective cross-functional communication make candidates stand out in this role. These competencies are crucial for ensuring that clinical trial documentation is complete, inspection-ready, and compliant with industry regulations.
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Cities with the most Etmf job openings:
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The most popular types of Etmf jobs are:
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Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC
Cambridge, MA • On-site, Remote
Full-time
Re-posted 3 days ago
Job description
Associate Manager/Manager, Clinical Systems (CTMS, eTMF), CDOC
Who we are:
At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture - one that sparks bold thinking and strengthens our connections with each other and with the rare disease communities we serve. We embrace diverse backgrounds with respect, active listening, and a commitment to inclusion - because our differences shape how we hire, collaborate, and innovate. Our team's proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities. Our commitment is more than scientific - it's deeply personal, grounded in the meaningful connections we have built. To learn more, visit www.agios.com and follow Agios on LinkedIn and X.
The impact you will make:
Agios Pharmaceuticals is searching for a dynamic Associate Manager/Manager, Clinical Systems (CTMS, eTMF) to join our growing team, is accountable for day-to-day clinical business systems operations, ensuring systems are designed and implemented with appropriate controls and are successfully adopted. In partnership with the AD, Clinical Systems and Sr. Manager, Clinical Systems, the Associate Manager/Manager, Clinical Systems serves as the Clinical Business Administrator for key clinical trial systems, including CTMS and eTMF.
What you will do:
- Support and/or function as a Clinical Business Administrator for CTMS and eTMF.
- Serve as a CTMS and eTMF Subject Matter Expert (SME), providing end-user support and troubleshooting to diagnose and resolve system issues.
- Partner with the business to understand use cases and/or system needs, and deliver system changes and configuration updates that support organizational adoption of the CTMS and eTMF platform.
- Alongside the Sr. Manager, Clinical Systems, coordinate and support ongoing computer system validation activities in alignment with product releases and/or configuration updates or enhancements. Collaborate with IT, QA and the Business System Owner to implement system change management.
- Contribute to standard operating procedures, work-instructions, and training material creation and/or revision, in partnership with multiple stakeholders across the R&D organization.
- Identify opportunities to enhance system functionality by evaluating system releases against business requirements, recommending configuration updates for CTMS and eTMF. Partner with impacted functions to assess the need and readiness for implementation.
- May assist in management of additional clinical technologies, as assigned, that are leveraged in clinical trials, developing system vendor strategy, partner selection, system standards and internal processes to ensure compliant systems development and operations.
What you bring:
- Bachelor's degree and 3+ years relevant work experience with CTMS and eTMF implementation and support
- Experience with computer system validation of GxP systems strongly preferred
- An ideal candidate will have direct experience with Veeva CTMS and eTMF
- Strong project management skills, and ability to effectively support system design discussions and collaborate with various business functions
- High attention to detail including proven ability to manage multiple, competing priorities
- Demonstrated ability to influence change
- Excellent written and oral communication skills
- Flexibility and cross functional collaboration
Concerned that you don't check off every box in the requirements listed above? Please apply anyway! At Agios, we value each other's differences and recognize that teams thrive when everyone brings their unique experiences to the table. We are dedicated to building an inclusive, diverse, equitable, and accessible environment where all employees can bring their whole selves to work. If you're excited about this role but your previous experience doesn't align perfectly with the job description, we still encourage you to apply. You may be just the right candidate for this role or another opening!
Work Location:
Location Agnostic: Work location for this role is based on employee's individual preference. This role has the ability to be either remote in the US or hybrid in our Cambridge Headquarters. Hybrid schedules vary but are generally less than 3 days per week onsite and hybrid employees are expected to live within commutable distance to our Cambridge Headquarters. Remote employees work entirely from home except for attending Company sponsored events/ meetings. For employees who choose to work remotely, travel may be required for certain company events commensurate to the above job description..
What we will give you:
- Deliberate Development. Your professional growth as one of our top priorities.
- Flexibility. We're all about individual needs. We embrace different perspectives, work styles, health and wellness approaches, care of families and productivity. When you're at your best, we're at our best.
- Premium benefits package. We invest in the health, wellbeing, and security of our people with a premium benefits package that is well-rounded and flexible to help meet the varied personal and professional needs of every member of our team. For more detail on the benefits we offer at Agios, visit the Inside Agios section of our website.
- Competitive and equitable performance-based compensation. This includes base salary and both short- and long-term incentives that are connected to our business strategy and vary based on individual and company performance.
- The current base salary range for this position at the Associate Manager level is expected to be between $94,025 and $141,038 annualized and the current base salary range for this position at the Manager level is expected to be between $110,029 and $165,044 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.
- Psychological safety. We support an environment of fearlessness. We want you to share your ideas, speak candidly and take data-informed risks to help push the boundaries.
- Commitment to diversity. We strive to foster a welcoming workplace where everyone can thrive. We're continuously looking to improve the inclusivity of our workforce.
- Commitment to community. We're an active participant in the communities that surround us - the communities where we live, and the community of people and their loved ones in need of better treatment options for conditions that are often overlooked.
Interested in learning more about what makes our culture unique? Visit the Inside Agios section of our website.
Employment Type: Full timeAbout Agios Pharmaceuticals
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
201 - 500 Employees
Headquarters location
Cambridge, MA, US
Year founded
2008