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$107.3K

$189K

How much do dm clinical research jobs pay per year?

As of Jul 29, 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.

Is DM clinical research legit?

DM Clinical Research is a clinical research organization that conducts trials and studies in the healthcare industry. Its legitimacy can be verified through industry accreditation, client reviews, and regulatory compliance with agencies like the FDA. Job seekers should research the company's reputation and ensure it adheres to ethical standards in clinical research.

How much does DM clinical research pay?

The salary for a DM Clinical Research role typically ranges from $60,000 to $120,000 annually, depending on experience, location, and specific responsibilities. Entry-level positions may start lower, while experienced professionals or those with specialized skills can earn higher salaries, often supplemented with benefits and bonuses.

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 a DM in clinical research?

A DM in clinical research stands for Data Manager, responsible for designing data collection tools, ensuring data quality, and managing databases for clinical trials. They work closely with study teams and often use electronic data capture systems to maintain accurate trial data.

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 highest paying job in clinical research?

In clinical research, senior roles such as Clinical Research Director or Vice President of Clinical Operations typically have the highest salaries, often exceeding six figures annually. These positions require extensive experience, leadership skills, and often advanced certifications or degrees in related fields.

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 July 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Unblinded Clinical Research Coordinator II

Unblinded Clinical Research Coordinator II

DM Clinical Research

Jersey City, NJ • On-site

$25.25 - $33.75/hr

Full-time

Posted 17 days ago

Job description

Unblinded Clinical Research Coordinator
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
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