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Unblinded Study Jobs (NOW HIRING)

DM Clinical

Certified Medical Assistant (4063)

Irving, TX · On-site

$16.25 - $21/hr

Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure ... or Unblinded, required * 1+ year utilizing CRIO, preferred Credentials: * LPN (Licensed ...

DM Clinical

Registered Nurse (4122)

Brooklyn, NY · On-site

$65K - $85K/yr

... a Unblinded CRC to join our team. This individual will be responsible for dispensing ... Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure ...

DM Clinical Research

Pharmacist

Jersey City, NJ · On-site

$123K - $147K/yr

Ensure compliance with study-specific blinding plans. * Provide consultative support regarding the ... for an Unblinded Clinical Research Coordinator to join our team. This individual will be ...

Headlands Research

Pharmacy Technician

San Diego, CA · On-site +1

$18.50 - $22.50/hr

Opportunity to contribute to meaningful metabolic and immunologic studies * Backing of a growing ... Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.

Headlands Research

[[AMCR]] Pharmacy Technician

Escondido, CA · Hybrid

$18.25 - $22.25/hr

Opportunity to contribute to meaningful metabolic and immunologic studies * Backing of a growing ... Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.

Headlands Research

[[AMCR]] Pharmacy Technician

Escondido, CA · On-site

$18.25 - $22.25/hr

Opportunity to contribute to meaningful metabolic and immunologic studies * Backing of a growing ... Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.

Headlands Research

Pharmacy Technician

San Diego, CA · On-site

$18.50 - $22.50/hr

Opportunity to contribute to meaningful metabolic and immunologic studies * Backing of a growing ... Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.

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Unblinded Study information

What is an unblinded study?

An unblinded study is a type of clinical research in which both the researchers and participants know which treatment or intervention is being administered. This contrasts with blinded studies, where one or both parties are unaware of the treatment allocation to reduce bias. Unblinded studies are often used when blinding is not feasible, such as in surgical interventions or certain behavioral studies. While they are easier to conduct, unblinded studies can be more susceptible to bias, so results must be interpreted carefully.

What are the key skills and qualifications needed to thrive as an unblinded study coordinator, and why are they important?

To thrive as an Unblinded Study Coordinator, you need a background in life sciences, clinical research experience, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and relevant certifications like ACRP or SOCRA is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for success in this role. These skills ensure protocol adherence, data integrity, and seamless collaboration with study teams in regulated clinical trial environments.

What are some common challenges faced by professionals working on unblinded studies, and how can they be addressed?

Professionals involved in unblinded studies often face challenges related to maintaining objectivity and minimizing bias, since both participants and researchers are aware of the treatment being administered. This can influence data collection and interpretation. To address these challenges, teams typically implement rigorous protocols, frequent training, and independent data monitoring. Additionally, clear documentation and adherence to Good Clinical Practice (GCP) help ensure data integrity and regulatory compliance throughout the study.

What is the difference between Unblinded Study vs Data Analyst?

AspectUnblinded StudyData Analyst
CredentialsTypically requires clinical research training, certifications in Good Clinical Practice (GCP)Requires degrees in statistics, mathematics, or related fields; certifications like CAP or Microsoft Excel certifications are common
Work EnvironmentClinical research settings, hospitals, or research organizationsOffice environments, data centers, or remote work
Industry UsagePharmaceuticals, clinical research organizations, healthcareVarious industries including healthcare, finance, marketing

Unblinded Study professionals focus on clinical trial phases where treatment groups are revealed, requiring clinical knowledge. Data Analysts interpret data across industries, including healthcare, often working with large datasets. While both roles involve data handling, their environments, credentials, and industry applications differ significantly.

More about Unblinded Study jobs

What job categories do people searching Unblinded Study jobs look for?

The top searched job categories for Unblinded Study jobs are:

Unblinded Study jobs near you
Infographic showing various Unblinded Study job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Clinical Research Nurse- PRN

ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES

Murfreesboro, TN • On-site

Per diem

This job post has expired 3 days ago. Applications are no longer accepted.

Job description

Description:

We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.


Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care. We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Nurse to join our Research department.


The Clinical Research Nurse (CRN) reports to the Director of Research and is responsible for managing assigned unblinded protocols in compliance with Protocol, FDA CFR, GCP and company SOPs. The CRN will work independently as primary pharmacy designee for unblinded clinical trials in Arizona. The CRN will travel to all sites as needed to prepare investigational medication for subcutaneous injections or intravenous infusions. The CRN will also attend meetings, monitoring visits and has the opportunity to work from home when not needed on site.


Responsibilities:

  • Manages all assigned clinical trials unblinded pharmacy responsibilities
  • Travels to sites approximately 2-3 days per week to prepare investigational medication 
  • Responsible for preparation of unblinded clinical trial medications for IV Or SC administration.
  • Performs dispensation of investigational product (IP) using web-based drug dispensation transactions
  • Ensures correct dose and medication is prepared for each subject visit
  • Perform subcutaneous administration for unblinded trials
  • Responsible for the chain of custody and accurate accountability of investigational products and devices
  • Ensures uniform implementation of protocols by completing the required training documentation in a consistent, accurate and timely manner.  
  • Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards. 
  • Provides all employees and research subjects with excellent service experience by consistently demonstrating professional decorum.





Requirements:

Minimum Qualifications:

  • Licensed Registered Nurse (RN) or Licensed Practical Nurse (LPN)
  • Infusion experience preferred
  • Clinical research experience preferred
  • Possess strong organizational skills 
  • Maintains confidentiality of patient and study information
  • Excellent verbal and written communication skills 
  • Reliable method of transportation