Biosafety Analyst

WCG

. Provide scientific review and analysis for hospitals, clinics, laboratories, and other institutions .

Posted 11/3/2026full-timeRemote • United StatesJuniorMid-Level💰 $58,860 - $91,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in scientific review and analysis within clinical and biomedical research settings, with a strong understanding of NIH Guidelines and biosafety compliance. Capable of providing guidance on human gene transfer studies and facilitating institutional training and improvement initiatives.

Highest-signal resume keywords

Scientific ReviewNIH Guidelines ComplianceClinical Safety MeasuresBiomedical TerminologyInstitutional Training Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchBiomedical ResearchHuman Gene Transfer StudiesBiosafety Program ImprovementInstitutional Review Board (IBC) Analysis

Soft Skills

CommunicationTraining FacilitationMeeting CoordinationAttention to Detail

Industry Keywords

Life SciencesPharmaceutical ResearchMicrobiologyBloodborne PathogensClinical Studies

About the role

Key responsibilities & impact

Provide scientific review and analysis for hospitals, clinics, laboratories, and other institutions
Analyze institutional training, facilities, and operations for IBC review preparation
Provide guidance to institutional personnel on human gene transfer clinical studies and laboratory research projects
Educate institutions on compliance with NIH Guidelines and affiliated regulations
Help institutions identify biosafety program improvements
Ensure assigned studies are reviewed by the IBC before approval expiration
Identify training opportunities and participate in teleconference-based client orientations and training
Contribute to continuous improvement initiatives within the IBC group
Host teleconference-based convened IBC meetings
Record meeting minutes
Assist institutions with IBC recommendations and conditions of approval
Perform other duties assigned by the supervisor

Requirements

What you’ll need

Bachelor's degree in life sciences or a related field
At least 2 years’ experience in a clinical, pharmaceutical, or biomedical research setting
Basic understanding of biomedical terminology, human disease, microbiology and bloodborne pathogens, and clinical safety measures
Ability to analyze institutional training, facilities, and operations
Ability to provide guidance on IBC review of human gene transfer clinical studies and/or laboratory research projects
Knowledge of the NIH Guidelines for Research with Recombinant and Synthetic Nucleic Acid Molecules and affiliated regulations
Attendance and punctuality are essential
Willingness to travel 0–5%

Benefits

Comp & perks

Medical, dental, vision, life and disability insurance
401(k) with company match
Flexible spending accounts
Employee assistance programs
Work/life balance tools
Referral bonuses
Tuition reimbursement
On-the-job training
Certification assistance
Continuing education support
Paid holidays
Vacation
Sick time
Career development opportunities across One WCG