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Dm Clinical Research Jobs (NOW HIRING)

DM Clinical Research

Pharmacist

Jersey City, NJ

$123K - $147K/yr

Pharmacist DM Clinical Research is looking for a Pharmacist to fill our Unblinded Clinical Research Coordinator role and join our team. This individual will be responsible for dispensing ...

DM Clinical Research

Pharmacist

New York, NY

$63.75 - $76.50/hr

Pharmacist DM Clinical Research is looking for a Pharmacist to fill our Unblinded Clinical Research Coordinator role and join our team in New Jersey. This individual will be responsible for ...

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 ...

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$49K

$107.3K

$189K

How much do dm clinical research jobs pay per year?

As of Aug 9, 2026, the average yearly pay for dm clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

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 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 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.

More about Dm Clinical Research jobs
What cities are hiring for Dm Clinical Research jobs? Cities with the most Dm Clinical Research job openings:
What states have the most Dm Clinical Research jobs? States with the most job openings for Dm Clinical Research jobs include:
What job categories do people searching Dm Clinical Research jobs look for? The top searched job categories for Dm Clinical Research jobs are:
Dm Clinical Research jobs near you
Infographic showing various Dm Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Unblinded Clinical Research Coordinator II (3980)

DM CLINICAL RESEARCH GROUP

Sugar Land, TX

$21.75 - $29/hr

Full-time

Posted 16 days ago

Job description

DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Pharmacy Technicians, LPN's and CMA's are encouraged to apply!
Duties & Responsibilities:

  • Compound and dispense prescribed IP as needed by Sponsor approved protocol
  • Study IP management
  • Provide training and guidance for new team members
  • Assist in all aspects of company start up activities as required
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans
  • Perform regular audits on the clinical data to assess percent completeness and accuracy
  • Assist in onboarding training for new members
  • Ensure external sites’ regulatory documents and required site certifications are up to date
  • Provide consultative support regarding the preparation and dosing of drugs
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials
  • Understand and apply all applicable site procedures
  • Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
  • Develop operating procedures, guides and best practices for data entry portals and project workflows
  • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.
  • Any other duties or tasks assigned by the manager

KNOWLEDGE & EXPERIENCE


Education:

  • Associates Degree required or 2 years of formal educational coursework
  • Bachelor's degree, preferred
  • Secondary or Foreign Medical Graduate, preferred

Experience:

  • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
  • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
  • 1+ year utilizing CRIO, preferred


Credentials:

  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
  • Pharmacy Technician Certification, preferred
  • Completion of DMCR-required training, including GCP, OSHA and IATA


Knowledge and Skills:

  • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
  • Excellent communication and customer service skills, both written and verbal
  • Excellent time-management skills
  • Ability to remain composed under pressure and high-stress situations
  • Outgoing personality
  • Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred

Apply