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From Home Clinical Research Rater Jobs (NOW HIRING)

Alcanza Clinical Research

Clinical Rater/ Counselor

Katy, TX · On-site

$54K - $72K/yr

The Clinical Rater will be responsible for interviewing research participants and their informants/caregivers, who are being evaluated to participate in a research study for various health conditions ...

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From Home Clinical Research Rater information

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How much do from home clinical research rater jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for from home clinical research rater in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is the difference between From Home Clinical Research Rater vs From Home Clinical Trial Coordinator?

AspectFrom Home Clinical Research RaterFrom Home Clinical Trial Coordinator
CredentialsTypically requires a high school diploma or equivalent; some roles prefer healthcare or research experienceRequires a bachelor's degree in health sciences, nursing, or related fields; certification may be preferred
Work EnvironmentRemote, primarily computer-based, evaluating patient data and reportsPrimarily remote or hybrid; involves coordinating trial activities, communicating with sites and sponsors
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for data evaluationUsed by clinical research sites, pharmaceutical companies, and CROs for trial management

While both roles are involved in clinical research, From Home Clinical Research Raters focus on evaluating patient data remotely, whereas From Home Clinical Trial Coordinators manage trial logistics and communication. Understanding these differences helps job seekers identify the right position based on their skills and credentials.

Can I get paid to participate in trials?

As a From Home Clinical Research Rater, you typically do not get paid to participate in clinical trials; instead, you are usually hired to evaluate and rate trial data or patient responses remotely. Participating as a trial volunteer is generally unpaid, but some research studies may offer compensation for participation. The role of a remote rater involves reviewing trial materials and providing assessments rather than participating as a subject in the trial itself.

Who makes more, CRC or CRA?

In clinical research, a Clinical Research Associate (CRA) typically earns more than a Clinical Research Coordinator (CRC). CRAs often have higher salaries due to their responsibilities overseeing multiple sites, monitoring trials, and requiring specialized knowledge, while CRCs handle site-level tasks and patient interactions. Salary differences can vary based on experience, location, and certifications, but generally, CRAs have higher compensation in the industry.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, understanding of Good Clinical Practice (GCP), and sometimes certification. Entry-level roles in clinical research may include Clinical Trial Assistant or Research Coordinator, with CRAs often advancing from these positions after gaining relevant experience.

How can I make 2000 a week working from home?

A From Home Clinical Research Rater can potentially earn $2000 weekly by working full-time hours, often 40 or more hours, and gaining experience or certifications that increase pay rates. Earning this amount typically requires consistent effort, efficient time management, and possibly supplementing with additional tasks or higher-paying projects within the role.
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From Home Clinical Research Rater jobs near you
Unblinded Clinical Research Coordinator II

Unblinded Clinical Research Coordinator II

DM Clinical Research

Jersey City, NJ

$25.25 - $33.75/hr

Full-time

Posted 25 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