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Unblinded Study Jobs (NOW HIRING)

DM Clinical Research

Pharmacist

Jersey City, NJ

$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 · Hybrid

$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.

DM Clinical Research

Pharmacist

New York, NY

$63.75 - $76.50/hr

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

$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.

ProPharma Group

Biostatistician

Western Springs, IL · On-site

Independently reads and comprehends study design and statistical sections of a protocol and ... Participates in unblinding activities and incorporates unblinded treatment codes into algorithms ...

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All JobsUnblinded Study Jobs

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 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.

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 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.
More about Unblinded Study jobs
What cities are hiring for Unblinded Study jobs? Cities with the most Unblinded Study job openings:
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 June 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 1% Physical, and 99% Hybrid job distribution.

Unblinded Clinical Research Coordinator II (3605)

DM CLINICAL RESEARCH GROUP

Bradenton, FL • On-site

$22 - $29.25/hr

Other

Posted 25 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.
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

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