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Unblinded Study Jobs (NOW HIRING)

ProPharma Group

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

New

ProPharma Group

Biostatistician

Charleston, WV

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

New

Cartesian Therapeutics

Medical Director

Frederick, MD · On-site

Serve as sponsor medical monitor for the Phase 3 AURORA study in generalized myasthenia gravis ... Collaborate with Biostatistics and Data Management teams in ongoing blinded and unblinded data ...

New

Cartesian Therapeutics

Medical Director

Frederick, MD · Remote

Serve as sponsor medical monitor for the Phase 3 AURORA study in generalized myasthenia gravis ... Collaborate with Biostatistics and Data Management teams in ongoing blinded and unblinded data ...

New

Vor Bio

Director, Biostatistics

Boston, MA · On-site

Serve as the study and program-level statistical lead for one or more clinical programs, with end ... Oversee IDMC/DSMB activities including charter and SAP development, preparation of unblinded ...

EDETEK

Senior Biostatistician

Contribute statistical input to study design, sample size determination, endpoint definition ... Work effectively within blinded and unblinded team structures and maintain strict confidentiality.

Parexel

OR · On-site

During study conduct, serve as the primary point of contact for assigned investigator sites. Work ... May undertake the responsibilities of an unblinded monitor where appropriate Clinical/Scientific ...

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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 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.
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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.
Biostatistician

Biostatistician

ProPharma Group

On-site

Full-time

Posted 2 days ago

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Essential Functions:

  • Independently reads and comprehends study design and statistical sections of a protocol and appropriately adapts protocol language to a statistical analysis plan.

  • Independently able to perform or QC sample size calculations when provided with required operational design information.

  • Able to review data management documents to assess quality of the documents to support statistical analyses with supervision of more senior staff.

  • Develop Randomization specifications and programs based on study requirements with supervision of more senior staff.

  • Prepares draft statistical analysis plans and shells with support and oversight of senior staff.

  • With support and oversight of senor staff: Reviews PD for exclusion from analysis sets and implements into specifications and/or programs.

  • Participates in unblinding activities and incorporates unblinded treatment codes into algorithms/programming

  • Able to read and understand common SDTM & ADaM domains and mapping algorithms. Able to review common domains with oversight. Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC.

  • Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or more complex data sets with senior oversight.

  • Independently reads and comprehends study design and statistical sections of a protocol and appropriately adapts protocol language to a statistical analysis plan.

  • Independently able to perform or QC sample size calculations when provided with required operational design information.

  • Able to review data management documents to assess quality of the documents to support statistical analyses with supervision of more senior staff.

  • Develop Randomization specifications and programs based on study requirements with supervision of more senior staff.

  • Prepares draft statistical analysis plans and shells with support and oversight of senior staff.

  • With support and oversight of senor staff: Reviews PD for exclusion from analysis sets and implements into specifications and/or programs.

  • Participates in unblinding activities and incorporates unblinded treatment codes into algorithms/programming

  • Able to read and understand common SDTM & ADaM domains and mapping algorithms. Able to review common domains with oversight. Learns the role that SDTM & ADaM plays in the standardization of clinical trials data/CDISC.

  • Able to prepare specifications for simple analysis data sets (CDISC and CDISC-like) independently or more complex data sets with senior oversight.

  • Able to develop programs to produce and perform statistical review of datasets, listings, tables and graphs as outlined by a statistical analysis plan.

  • Able to effectively QC TLFs, SDTM and analysis data sets (ADaM/non-ADaM) with supervision of senior staff.

  • Able to review the statistical section of CSR for statistical accuracy.

  • Able to support the lead statistician in maintaining biostatistical section of TMF

  • Able to attend project team meetings as required.

  • Able to interact with both internal and external clients on project issues with supervision of senior staff.

  • Respects and maintain the confidentiality of the processed material and ensure that any regulations concerning security or confidentiality (such as the safeguarding of passwords) are complied with

  • Able to keep detailed records of time spent on each project to allow accurate billing

  • Develops and maintains overall awareness in the field of biostatistics by reading related literature, attending training classes, professional meetings, statistical conferences etc.

  • Develops knowledge of clinical research including awareness and understanding of how biostatistics interacts with other team members on a project.

  • Perform other work-related duties as assigned

Necessary Skills and Abilities:

  • In-depth knowledge of statistical methodologies.

  • Demonstrated working knowledge of basic clinical trial design and analysis principles.

  • Working knowledge of CDISC standards and application of these standards to projects.

  • Strong computer skills, with evidence of programming skills (SAS or R) especially statistical inferential procedures

  • Excellent English Communication skills (verbal, written & interpersonal).

  • Detail oriented, well organized.

  • Ability to multitask and work effectively in a fast-paced environment with changing priorities.

  • Excellent Communication and interpersonal skills, with the ability to work collaboratively in cross functional teams and with external partners.

  • Excellent team player, collaborative and able to work as part of an effective team. Maintains a positive, results orientated work environment

Educational Requirements:

  • Advanced degree (MS or PhD) from accredited college or university, in statistics or closely related field. Equivalent combination of education, training and experience will be considered.

Experience Requirements:

  • Minimum 2-4 years' experience in clinical trials design and analysis or related field

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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