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Dm Clinical Jobs in Spring, TX (NOW HIRING)

DM Clinical

Site Manager (4138)

Houston, TX · On-site

Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...

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DM Clinical Research

Research Assistant

Houston, TX

$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 ...

DM Clinical Research

Regulatory Specialist

Houston, TX · Hybrid

Regulatory Specialist (Hybrid) A Clinical Research Regulatory Specialist works closely with our Clinical Research staff to provide excellent regulatory oversight for our clinical trials. To ensure ...

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Showing results 21-40

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 21, 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 is a dm clinical?

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?

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 the key skills and qualifications needed to thrive as a clinical research coordinator at dm clinical?

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 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 August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,346 per year, or $39.1 per hour.

Clinical Research Site Manager

DM Clinical Research

Tomball, TX

Full-time

Re-posted 8 days ago

Job description

Clinical Research Site Manager
The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Also To ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely basis.

DUTIES amp; RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
  • Responsible for immediate supervision and performance of the assigned site staff under the supervision of the Site Director or Director of Site Operations.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • It is the responsibility of the Site Manager to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow-up on the action items, at their respective sites.
  • Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs, and guidance documents.
  • Ensuring data quality, subject retention, and compliance, timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling, and disciplining the employees as applicable.
  • To develop, coordinate, and enforce site-specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management to the site team.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Any other matters as assigned by management.
KNOWLEDGE amp; EXPERIENCE
Education:
  • Bachelor’s degree preferred
  • Advanced degree preferred
Experience:
  • At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization.
Credentials:
  • Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
Knowledge and Skills:
  • Solid teamwork, organizational, interpersonal, and problem-solving skills and attention to detail.
  • Critical Thinking
  • Active Listening
  • Reading Comprehension — Understanding written sentences and paragraphs in work-related documents.
  • Speaking and Writing to communicate effectively as appropriate for the needs of the audience.
  • Ability to multitask, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
  • Strong computer skills in relevant software and related clinical systems are required.
  • Comprehensive knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs.

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