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Dm Clinical Jobs in Spring, TX (NOW HIRING)

DM Clinical Research

Administrative Assistant

Houston, TX · On-site

$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 · On-site

$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

Study Manager I (4012)

Houston, TX · On-site

Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s) * Creating and or Reviewing ...

New

DM Clinical

CRC II (3996)

Houston, TX · On-site

$21.75 - $29/hr

The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP ...

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All JobsDm Clinical JobsDm Clinical Jobs in Spring, TX

Dm Clinical information

See Spring, TX salary details

$53.8K

$81.3K

$103.7K

How much do dm clinical jobs pay per year?

As of Aug 3, 2026, the average yearly pay for dm clinical in Spring, TX is $81,346.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $89,900.00 per year, depending on experience, location, and employer.

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

To thrive as a Clinical Research Coordinator at DM Clinical, you need a background in life sciences or healthcare, experience in clinical research, and often a bachelor's degree or higher. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are typically required. Attention to detail, organizational skills, effective communication, and the ability to multitask are standout soft skills for this role. These skills ensure clinical trials are conducted efficiently, safely, and in compliance with regulatory standards, supporting successful research outcomes.

What is the difference between Dm Clinical vs Dm Radiology?

AspectDm ClinicalDm Radiology
Required CredentialsDiploma in Medical Clinical Practice, relevant certificationsDiploma in Medical Radiology, relevant certifications
Work EnvironmentHospitals, clinics, outpatient centersHospitals, imaging centers, diagnostic labs
Industry UsagePatient care, clinical proceduresImaging, diagnostic procedures

Dm Clinical professionals focus on patient care and clinical procedures, working mainly in hospitals and clinics. Dm Radiology specialists concentrate on diagnostic imaging, such as X-rays and MRIs, often working in imaging centers. Both roles require relevant certifications and are essential in healthcare, but they differ in their focus and work environment.

What is a DM Clinical and what do they do?

A DM Clinical typically refers to a professional involved in clinical data management (CDM) within the healthcare or pharmaceutical industries. Their main responsibility is to ensure that clinical trial data is collected, managed, and reported accurately and securely. They work closely with clinical research teams to design data collection systems, oversee data entry and validation, and ensure compliance with regulatory standards. This role is critical for the integrity of clinical trials and the success of drug development processes.

What are the main responsibilities of a clinical research coordinator at DM Clinical, and how does the role contribute to successful clinical trials?

As a clinical research coordinator at DM Clinical, you will be responsible for managing daily operations of clinical trials, including patient recruitment, data collection, and ensuring compliance with study protocols and regulatory guidelines. The role requires close collaboration with principal investigators, sponsors, and other site staff to maintain study integrity and participant safety. By efficiently handling logistical and administrative tasks, you help facilitate smooth trial execution, which is essential for generating reliable data and supporting advancements in medical research.
What are popular job titles related to Dm Clinical jobs in Spring, TX? For Dm Clinical jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Dm Clinical jobs in Spring, TX look for? The top searched job categories for Dm Clinical jobs in Spring, TX are:
Dm Clinical jobs near you
Infographic showing various Dm Clinical job openings in Spring, TX as of July 2026, with employment types broken down into 81% Full Time, 12% Part Time, and 7% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,346 per year, or $39.1 per hour.

Site System Associate II

DM Clinical Research

Houston, TX • On-site

Full-time

Re-posted 27 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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