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Ctms Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

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 ...

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Ctms information

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$14

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How much do ctms jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for ctms in the United States is $14.60, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $15.14 per hour, depending on experience, location, and employer.

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.

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What states have the most Ctms jobs? States with the most job openings for Ctms jobs include:
Clinical Data Analyst

Contractor

Posted yesterday


Job description

Company 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

Job Description

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


Qualifications

Education: Must have a four year college degree and at least 8 years of professional experience

Medidata CTMS Super Amin experience preferred

Additional Information

Please Feel Free to Forward your resume on [email protected] and You can directly contact me @ 7324291635


Integrated Resources logo

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