Clinical Scientist – Consultant

Job not on LinkedIn

🔥 18 hours ago

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 12%

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

TScan Therapeutics

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2018

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

TScan Therapeutics is a clinical-stage biopharmaceutical company dedicated to changing lives by discovering new cancer targets and developing safe and effective T cell therapies for patients. Their innovative approach involves leveraging insights from patients who have successfully fought cancer to inform the development of new treatments. TScan is focused on unleashing the untapped potential of the human immune system to create impactful T cell therapies for various malignancies.

📋 Description

• Interpret clinical data to generate high-quality summaries and insights supporting regulatory filings, publications, and scientific communications • Collaborate cross-functionally with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Business Operations across clinical phases • Lead or support authoring selected sections of clinical study reports in partnership with Medical Directors • Support real-time data review, identify safety and efficacy trends, assess protocol compliance, and review protocol deviations • Escalate appropriate issues to Medical Monitors • Identify scientific and clinical quality issues for discussion with principal investigators and study sites • Partner with study teams and GCP quality team members on escalations • Consult on study-specific case report form design and author CRF completion guideline sections • Ensure CRFs align with study requirements during user acceptance testing • Perform safety and efficacy reviews for Data Monitoring Committee preparation • Analyze trends within and across clinical programs • Collaborate with Business Operations and Data Management on clinical data technology access, retention, and visualization strategy • Support integration of new tools and technologies into phase 1-3 clinical studies

🎯 Requirements

• Ph.D., PharmD, MD, Nursing, or Clinical Master’s degree in a scientifically relevant field • 6+ years of clinical development experience within the biotechnology or pharmaceutical industry • Proven understanding of clinical development processes for phase 1-3 clinical studies • Previous experience identifying trends and setting risk mitigation strategies with Medical teams within clinical studies • Demonstrated experience designing and executing clinical trials • Strong understanding of GCP/ICH guidelines and regulatory expectations • Experience in rare disease and/or neuromuscular disease is strongly preferred • Skilled in Microsoft suite and innovative data review tools, including patient profiles and report generating tools • Self-motivated, with demonstrated success delivering assigned tasks according to timelines • Demonstrated creative problem-solving and learning ability • Ability to interpret complex data and communicate clearly with scientific and non-scientific stakeholders • Strong data analysis, data visualization, and communication skills • Ability to write clear, accurate, and concise documents, construct informative figures, and present to diverse audiences • Desire to work in an innovative, collaborative, fast-paced, mission-driven environment • US-based work eligibility/location requirement

🏖️ Benefits

• Flexible working environment • Remote work arrangement • Contract position with 40 hours per week expected • Minimum quarterly travel to Entrada Therapeutics Headquarters in Boston, MA

📊 Check your resume score for this job

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

Upload Resume