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Unblinded Study Jobs (NOW HIRING)

[[AMCR]] Pharmacy Technician

Escondido, CA ยท 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.

Pharmacy Technician

San Diego, CA ยท 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.

Pharmacy Technician

San Diego, CA ยท 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.

Oncology Infusion Nurse (RN)

Los Angeles, CA ยท On-site

$43.27 - $57.69/hr

Perform IV infusions of both blinded and unblinded investigational products in accordance with study protocols. * Obtain blood specimens and other biological samples from study participants using ...

Showing results 41-60

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
Infographic showing various Unblinded Study job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 71% In-person, and 29% Remote job distribution.

[[AMCR]] Pharmacy Technician

Headlands Research

Escondido, CA โ€ข On-site

$18.25 - $22.25/hr

Other

Posted 13 days ago


Job description

AMCR Pharmacy Technician

Escondido, California

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

For experienced Pharmacy Technicians looking for meaningful work in clinical research.

If you're a Pharmacy Technician who values precision, compliance, patient safety, and collaborative clinical environments, AMCR Institute may be the right next step in your career.

Our Escondido site is known for its strong operational infrastructure, experienced research teams, and commitment to advancing metabolic and immunologic research through high-quality clinical trials. This role offers the opportunity to work directly with investigational products and contribute to studies that support the development of innovative therapies.

Why Experienced Pharmacy Technicians Choose AMCR Institute
  • Exposure to complex investigational product management within clinical research
  • Collaborative environment with experienced investigators, coordinators, and clinical staff
  • Strong operational support, SOPs, and compliance-focused processes
  • Opportunity to contribute to meaningful metabolic and immunologic studies
  • Backing of a growing research network with resources and long-term stability

This role is ideal for Pharmacy Technicians who enjoy working in highly regulated environments, take pride in accuracy and documentation, and want to be part of a team advancing innovative medical research.

The Role:

The Pharmacy Technician plays a key role in the successful execution of clinical trials by ensuring the safe, accurate, and compliant handling of investigational products (IP). Working under the supervision of a licensed pharmacist or certified technician (as applicable), this individual will be responsible for receiving, storing, preparing, dispensing, documenting, and managing investigational drugs in accordance with study protocols, GCP/ICH regulations, and institutional SOPs. This role may also support administrative and data entry activities related to the conduct of clinical research.

Responsibilities:
  • Investigational Product (IP) Management
    • Receive, store, prepare, and dispense investigational products according to protocol, pharmacy manual, and regulatory requirements.
    • Use IWRS/IRT systems to log shipments, assign IP, and perform returns or destructions per study-specific guidance.
    • Maintain accurate inventory logs, temperature records, and expiration tracking for all IP and supplies.
    • Monitor and respond to temperature excursions, discrepancies, or deviations per SOP.
    • Perform aseptic preparations where required, following sterile technique protocols.
    • Manage IP accountability documentation, including blinded and unblinded logs and reconciliation.
    • Ensure all investigational product storage complies with GCP and institutional policies (double-locked, secure, labeled, etc.).
  • Documentation & Compliance
    • Maintain audit-ready records of all pharmacy activities, including temperature logs, equipment calibrations, and IP logs.
    • Create and manage pharmacy study binders with updated regulatory and protocol-specific content.
    • Adhere to ALCOA-C principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, and Consistent) in documentation practices.
    • Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.
  • Administrative & Operational Support
    • Assist with scheduling and performing protocol-specific assessments (e.g., memory assessments, vital signs, specimen collection support).
    • Perform data entry in eCRFs according to protocol and system-specific guidelines.
    • Support query resolution, documentation scanning, and other clerical duties (e.g., faxing, reminder calls).
    • Order pharmacy-related supplies and assist with equipment upkeep and calibrations.
    • Provide pharmacy support to other team members and backfill duties during absences.
  • Communication & Collaboration
    • Maintain clear, professional communication with study coordinators, monitors, sponsors, and clinical staff.
    • Participate in team meetings and training sessions to stay updated on protocols, SOPs, and compliance standards.
    • Demonstrate flexibility and professionalism in a fast-paced, regulated environment.
Requirements:
  • Completion of a recognized Pharmacy Technician program preferred.
  • Registration with relevant state or provincial licensing body (e.g., College of Pharmacists of BC) required where applicable.
  • Current certification in Good Clinical Practice (GCP) and/or willingness to complete GCP training.
  • Minimum of 1โ€“2 years of experience as a Pharmacy Technician, preferably in a clinical research or hospital setting.
  • Experience with IWRS/IRT systems, inventory control, and investigational product handling preferred.
  • Familiarity with Phase Iโ€“IV clinical trials and regulatory requirements an asset.
  • Strong organizational and documentation skills with high attention to detail.
  • Proficient in Microsoft Office and electronic data capture systems.
  • Ability to follow protocols, SOPs, and maintain regulatory compliance.
  • Strong communication and interpersonal skills.
  • Demonstrated ability to manage multiple tasks efficiently and work independently or as part of a team.
  • Professionalism, reliability, and commitment to patient safety and data integrity.
About AMCR

Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials. The site conducts studies focused on pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines. With a passionate and experienced team, AMCR Institute partners with sponsors and CROs to deliver meticulous research while prioritizing the care, safety, and confidentiality of every participant. By accelerating access to innovative therapies, the site makes a meaningful difference in the lives of the many affected by metabolic and immunologic conditions.

Who Thrives in This Role
  • Pharmacy Technicians who value structure, precision, and accountability
  • Professionals interested in transitioning into or growing within clinical research
  • Individuals who enjoy detailed documentation and investigational product management
  • Team-oriented professionals who value collaboration and operational excellence
  • Those motivated by contributing to innovative therapies and meaningful patient outcomes

Apply today if you're looking for a Pharmacy Technician role where your attention to detail, compliance expertise, and operational support directly contribute to advancing meaningful clinical research.

California Pay Range

$23 - $26 USD

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Need Assistance?

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.