Biosafety Analyst

🔥 47 minutes ago

🇺🇸 United States – Remote

💵 $58.9k - $91.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧐 Analyst

👻 Ghost score 0%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

WCG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💊 Pharmaceuticals

☁️ SaaS

💰 Private Equity Round - WCG on 2019-11

Healthcare • Pharmaceuticals • SaaS

WCG is a global clinical research services and technology company that supports sponsors, CROs, research sites, and institutions across the lifecycle of clinical trials. Founded as a leader in independent ethical review, WCG provides IRB and IBC review, data monitoring committees, site enablement and study start-up services, participant recruitment and retention, and data & insights (including benchmarking, statistical consulting, and AI-powered trial foresight). The company also offers a suite of technology platforms (e. g. , ClinSphere®, eReview Manager, Total Enrollment, Total Feasibility) and large protocol and performance datasets to help design, plan, and run trials more efficiently and compliantly. WCG positions itself as a partner to biopharma and medical research organizations to accelerate trial activation, improve enrollment, and ensure regulatory and ethical compliance.

📋 Description

• 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

• 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

• 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

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume