This is a Direct Hire role with the client Manage IVRS upload jobs Upload study specific IVRS data files from different vendors into Siebel eClinical CTMS on a daily basis Data validation, data ...
This is a Direct Hire role with the client Manage IVRS upload jobs Upload study specific IVRS data files from different vendors into Siebel eClinical CTMS on a daily basis Data validation, data ...
Associate Clinical Trial Manager
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Associate Clinical Trial Manager
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Director, Veeva Clinical CTMS Lead
La Jolla, CA · On-site
$83K - $114K/yr
Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...
Director, Veeva Clinical CTMS Lead
La Jolla, CA · On-site
$83K - $114K/yr
Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
Quick apply
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
Associate Clinical Trial Manager
San Diego, CA · On-site
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Quick apply
Associate Clinical Trial Manager
San Diego, CA · On-site
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Director, Veeva Clinical CTMS Lead
Cambridge, MA · On-site
$87K - $119K/yr
Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...
Director, Veeva Clinical CTMS Lead
Cambridge, MA · On-site
$87K - $119K/yr
Advanced knowledge of Veeva Clinical or other Clinical Trial Management Systems (CTMS) * Strong understanding of regulatory requirements and compliance in the pharmaceutical industry * Proven track ...
Solution Sales Specialist, CTMS / eTMF
San Diego, CA · On-site
$123K - $155K/yr
Strong knowledge of the biopharmaceutical Clinical Trials process: strong understanding of or past experience working within Clinical Operations teams, particularly CTMS (Clinical Trial Management ...
Solution Sales Specialist, CTMS / eTMF
San Diego, CA · On-site
$123K - $155K/yr
Strong knowledge of the biopharmaceutical Clinical Trials process: strong understanding of or past experience working within Clinical Operations teams, particularly CTMS (Clinical Trial Management ...
Work with Study Teams and partners during study build process to create/maintain the following in CTMS: * Study, Country, Site, Contacts, and Institution records * Create and set up templates such as ...
Work with Study Teams and partners during study build process to create/maintain the following in CTMS: * Study, Country, Site, Contacts, and Institution records * Create and set up templates such as ...
eSource Manager
$100K - $130K/yr
The role serves as the primary owner for quality, readiness, and usability of all CTMS templates, as well as continuous improvement, while collaborating cross-functionally to support efficient study ...
Quick apply
eSource Manager
$100K - $130K/yr
The role serves as the primary owner for quality, readiness, and usability of all CTMS templates, as well as continuous improvement, while collaborating cross-functionally to support efficient study ...
IT Clinical Project Manager II - Veeva Vault Clinical: CTMS & eTMF (Sponsor Dedicated - Remote; P...
CTMS & eTMF (Sponsor Dedicated - Remote; Preference for Hybrid Foster City, CA ) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.
IT Clinical Project Manager II - Veeva Vault Clinical: CTMS & eTMF (Sponsor Dedicated - Remote; P...
CTMS & eTMF (Sponsor Dedicated - Remote; Preference for Hybrid Foster City, CA ) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
Associate Clinical Trial Manager
San Diego, CA · On-site +1
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Associate Clinical Trial Manager
San Diego, CA · On-site +1
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Associate Clinical Trial Manager
South San Francisco, CA · On-site
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Quick apply
Associate Clinical Trial Manager
South San Francisco, CA · On-site
$122K - $137K/yr
Monitor eTMF/CTMS system performance, trouble shoot issues, and coordinate resolutions with vendor and/or study team members. * Support eTMF/CTMS system upgrades, patches, testing, and validation ...
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
Clinical Conductor CTMS * Advarra eSource +EDC * Veeva SiteVault eReg * Monday Work Management * SharePoint Pages & Training Workflows * Power Query/BI Dashboards * in the CTMS system for both ...
eSource Manager
Cambridge, MA · On-site
$100K - $130K/yr
The role serves as the primary owner for quality, readiness, and usability of all CTMS templates, as well as continuous improvement, while collaborating cross-functionally to support efficient study ...
eSource Manager
Cambridge, MA · On-site
$100K - $130K/yr
The role serves as the primary owner for quality, readiness, and usability of all CTMS templates, as well as continuous improvement, while collaborating cross-functionally to support efficient study ...
Clinical Data Analyst is responsible for CTMS and Grants Manager study build, maintenance, and support activities. Work with Study Teams and partners during study build process to create/maintain the ...
Clinical Data Analyst is responsible for CTMS and Grants Manager study build, maintenance, and support activities. Work with Study Teams and partners during study build process to create/maintain the ...
Lexington, MA Provide support within Clinical and other groups as required relating to company's Clinical Trials Management System (CTMS) to support Clinical business process, including design of ...
Lexington, MA Provide support within Clinical and other groups as required relating to company's Clinical Trials Management System (CTMS) to support Clinical business process, including design of ...
IT Clinical Project Manager II - Veeva Vault Clinical: CTMS & eTMF (Sponsor Dedicated - Remote; P...
Foster City, CA · On-site +1
CTMS & eTMF (Sponsor Dedicated - Remote; Preference for Hybrid Foster City, CA ) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer ...
IT Clinical Project Manager II - Veeva Vault Clinical: CTMS & eTMF (Sponsor Dedicated - Remote; P...
Foster City, CA · On-site +1
CTMS & eTMF (Sponsor Dedicated - Remote; Preference for Hybrid Foster City, CA ) Syneos Health ® is a leading fully-integrated life sciences services organization built to accelerate customer ...
Oncology CTMS / OnCore Optimization * Oversee oncology-specific CTMS workflows including study builds, calendars, subject tracking, milestone management, reporting, and financial interfaces.
Oncology CTMS / OnCore Optimization * Oversee oncology-specific CTMS workflows including study builds, calendars, subject tracking, milestone management, reporting, and financial interfaces.
Oncology CTMS / OnCore Optimization * Oversee oncology-specific CTMS workflows including study builds, calendars, subject tracking, milestone management, reporting, and financial interfaces.
Oncology CTMS / OnCore Optimization * Oversee oncology-specific CTMS workflows including study builds, calendars, subject tracking, milestone management, reporting, and financial interfaces.
Ctms information
See salary details
$5.29 - $6.36
0% of jobs
$6.36 - $7.43
0% of jobs
$7.43 - $8.50
0% of jobs
$8.50 - $9.57
0% of jobs
$9.57 - $10.64
0% of jobs
$10.64 - $11.71
7% of jobs
$11.71 - $12.78
6% of jobs
$12.78 - $13.85
8% of jobs
$13.93 is the 25th percentile. Wages below this are outliers.
$13.85 - $14.93
46% of jobs
$15.24 is the 75th percentile. Wages above this are outliers.
$14.93 - $16
25% of jobs
$16 - $17.07
7% of jobs
$5
$14
$17
How much do ctms jobs pay per hour?
What are the typical responsibilities of someone working in a CTMS-related role?
Professionals working with Clinical Trial Management Systems are responsible for maintaining and updating study data, overseeing trial documentation, and ensuring alignment with regulatory requirements. They often coordinate with clinical research teams, data managers, and regulatory authorities to secure timely and accurate trial progress. Common challenges include balancing multiple studies simultaneously and ensuring data integrity across all phases. The role offers opportunities to develop expertise in clinical operations and can be a strong stepping stone toward advanced positions in clinical project management. Daily responsibilities often involve system troubleshooting, user support, and facilitating communication between different departments.
What are the key skills and qualifications needed to thrive in the Ctms position, and why are they important?
To thrive in a CTMS (Clinical Trial Management System) role, you need a solid understanding of clinical research processes, data management, and regulatory compliance, generally supported by a degree in life sciences or related fields. Proficiency with CTMS software such as Medidata, Oracle Siebel, or Veeva Vault, along with familiarity with GCP (Good Clinical Practice) guidelines, is essential. Excellent organizational skills, attention to detail, and strong communication abilities distinguish outstanding candidates in this position. These skills ensure accurate trial documentation, streamlined workflows, and regulatory compliance in the complex field of clinical research.
What is a CTMS job?
A CTMS (Clinical Trial Management System) job typically involves managing and maintaining software used to track clinical trials. Professionals in this role ensure that study data, timelines, budgets, and regulatory compliance are properly documented and maintained. They may work in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions, collaborating with clinical teams to streamline trial operations. The role often requires knowledge of clinical trial processes, data management, and regulatory requirements.
Job description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
This is a Direct Hire role with the client
Manage IVRS upload jobs
Upload study specific IVRS data files from different vendors into Siebel eClinical CTMS on a daily basis
Data validation, data formatting, set attributes, and create profiles
Perform data quality checks
Query Siebel eClinical database tables for data discrepancies
Provide business support for Medidata CTMS
Study build
Create templates (Subject Visit, Visit Reports, etc.)
Contact & Organization creation
User account creation and maintenance
Skills needed:
Must have experience with Siebel eClinical, Oracle databases, SQL queries, IVRS
Medidata CTMS Super Amin experience preferred
Must be familiar with the Clinical Trials Management process
Education: Must have a four year college degree and at least 8 years of professional experience
Medidata CTMS Super Amin experience preferred
Please Feel Free to Forward your resume on [email protected] and You can directly contact me @ 7324291635
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996