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Dm Clinical Research Jobs in Spring, TX (NOW HIRING)

DM Clinical Research

Administrative Assistant

Houston, TX

$17.25 - $23.25/hr

... at DM Clinical Research. DUTIES amp; RESPONSIBILITIES * Completing DMCR-required training, including GCP. * Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines ...

DM Clinical Research

Lab Technician

Tomball, TX

$18 - $24/hr

Research Assistant (Lab Technician) DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an ...

DM Clinical Research

Lead Data Analyst

Houston, TX

Lead Data Analyst DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for a Lead Data Analyst to ...

DM Clinical Research

Research Assistant

Houston, TX · On-site

$18.25 - $25.25/hr

Research Assistant The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES amp; RESPONSIBILITIES: * Completing DMCR ...

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All JobsDm Clinical Research JobsDm Clinical Research Jobs in Spring, TX

Dm Clinical Research information

See Spring, TX salary details

$43.6K

$95.5K

$168.2K

How much do dm clinical research jobs pay per year?

As of Aug 31, 2026, the average yearly pay for dm clinical research in Spring, TX is $95,517.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $109,000.00 per year, depending on experience, location, and employer.

What is DM Clinical Research?

DM Clinical Research is a clinical trials management organization that partners with pharmaceutical and biotechnology companies to conduct clinical trials for new medications and treatments. They manage multiple research sites and help recruit patients, collect data, and ensure that trials meet regulatory standards. Their work is essential for bringing safe and effective new therapies to market by testing them through well-designed clinical studies.

What are the key skills and qualifications needed to thrive as a DM Clinical Research professional, and why are they important?

To thrive as a DM Clinical Research professional, you need a solid understanding of clinical trial processes, data management principles, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as CDM (Certified Data Manager) are commonly required. Attention to detail, analytical thinking, and effective communication are vital soft skills for ensuring data accuracy and collaborating with cross-functional teams. These skills and qualifications are essential for maintaining high data quality and regulatory compliance in clinical research projects.

What are some common challenges faced by professionals working at DM Clinical Research, and how can they be addressed?

Professionals at DM Clinical Research often encounter challenges such as adhering to strict regulatory guidelines, managing complex clinical trial protocols, and ensuring accurate data collection. These challenges can be addressed by maintaining strong communication with cross-functional teams, utilizing robust project management tools, and participating in ongoing training on compliance and best practices. Building collaborative relationships with investigators and sponsors also helps streamline workflows and resolve issues efficiently.

What is the difference between Dm Clinical Research vs Clinical Research Coordinator?

AspectDm Clinical ResearchClinical Research Coordinator
Required CredentialsTypically requires a degree in health sciences or related field, with certifications like CCRP or CCRAOften requires a bachelor's degree in health sciences, nursing, or related fields, with certifications like CCRP
Work EnvironmentWorks in clinical trial sites, hospitals, or research organizations, often under the supervision of principal investigatorsWorks at clinical trial sites, managing daily study activities and patient interactions
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutionsEmployed by hospitals, research centers, and clinical trial sites

While both roles involve managing clinical trials, Dm Clinical Research professionals often focus on overseeing multiple studies and ensuring compliance, whereas Clinical Research Coordinators handle day-to-day trial operations and patient coordination. Both roles require similar certifications and work in clinical settings, but their responsibilities differ in scope and focus.

What are popular job titles related to Dm Clinical Research jobs in Spring, TX?

For Dm Clinical Research jobs in Spring, TX, the most frequently searched job titles are:

What job categories do people searching Dm Clinical Research jobs in Spring, TX look for?

The top searched job categories for Dm Clinical Research jobs in Spring, TX are:

What cities near Spring, TX are hiring for Dm Clinical Research jobs?

Cities near Spring, TX with the most Dm Clinical Research job openings:

Dm Clinical Research jobs near you
Infographic showing various Dm Clinical Research job openings in Spring, TX as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $95,517 per year, or $45.9 per hour.

Site System Associate II

DM Clinical Research

Houston, TX • On-site

Full-time

Re-posted 26 days ago

Job description

Site System Associate II
The purpose of this position is to provide technical expertise and organize the support of the Site Systems such as eSource, eConsent, eRegulatory, Looker, etc..to all DM Clinical Research Sites. The incumbent will serve as the first point of contact for matters related to site systems. The incumbent will have to work closely with all branches of Central Services as well as other functional teams across DM Clinical Research. The incumbent may be involved in identifying and researching new tools/systems that may be useful for DM Clinical Research. The incumbent may also provide support during deployment based on Site System Manager guidance.
DUTIES amp; RESPONSIBILITIES
  • Perform the development of each study into the electronic source, setting up new users and giving them access to the system based on set internal policies.
  • Perform finance configuration-related tasks based on departmental needs.
  • Act as the primary point of contact for any site system-related queries and questions
  • Contribute to the configuration, migration, User Acceptance Testing (UAT), validation, implementation, and maintenance of the eSource, eConsent, eRegulatory, Payment system, transportation system, looker, and any systems that come under Site Systems.
  • Collaborate with Clinical Operations Leadership on Super-User strategy to broaden end-user support and training.
  • Responsible for any special projects and tasks assigned by the manager or senior leadership.
  • Provide relevant audit support during inspections.
  • Identify opportunities for continuous process improvement; recommend solutions and implement them as needed
  • Any other matters as assigned by management

KNOWLEDGE amp; EXPERIENCE
Education:
  • BA/BS degree required
Experience:
  • 6 month working experience required in site system OR candidate must have 2 year of Clinical Research work experience
Credentials:
  • N/A
Knowledge and Skills:
  • Knowledge of any following vendor system: eSource Design, transportation portal, eConsent portal
  • Ability to manage User management of vendor system on own
  • Ability to multitask, communicate with internal stakeholders and gather system requirements
  • Knowledge of general system workflows, GCP guidelines, ALCOA-C related to electronic systems in clinical research.

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