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Dm Clinical Jobs (NOW HIRING)

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

$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

Phlebotomist

Jersey City, NJ

$17.75 - $22.25/hr

Phlebotomist DM Clinical Research is looking for a Phlebotomist for our Lab Technician role to join our team. The Phlebotomist will be responsible for assisting the clinical research staff in ...

DM Clinical Research

Phlebotomist

New York, NY

$18.50 - $23.25/hr

Phlebotomist DM Clinical Research is looking for a Phlebotomist for our Lab Technician role to join our team. The Phlebotomist will be responsible for assisting the clinical research staff in ...

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 ...

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Dm Clinical information

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$60.5K

$91.4K

$116.5K

How much do dm clinical jobs pay per year?

As of Jun 30, 2026, the average yearly pay for dm clinical in the United States is $91,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,000.00 and $101,000.00 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.
More about Dm Clinical jobs
What cities are hiring for Dm Clinical jobs? Cities with the most Dm Clinical job openings:
What job categories do people searching Dm Clinical jobs look for? The top searched job categories for Dm Clinical jobs are:
Dm Clinical jobs near you
Infographic showing various Dm Clinical job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $91,412 per year, or $43.9 per hour.
Pharmacist

Pharmacist

DM Clinical Research

New York, NY

$63.75 - $76.50/hr

Full-time

Posted 18 days ago

Job description

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 dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • 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.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required
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 Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • 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.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required

Apply