
501 - 1000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
ImmunityBio, Inc. is a biotechnology company focused on developing innovative immunotherapies to enhance the immune system's ability to fight cancer and infectious diseases. By harnessing the power of the body’s immune response, ImmunityBio aims to provide breakthrough treatments that can improve patient outcomes and longevity in challenging diseases.
🕒 March 25
Improve your chances of getting an interview by checking your resume score before you apply.

501 - 1000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
ImmunityBio, Inc. is a biotechnology company focused on developing innovative immunotherapies to enhance the immune system's ability to fight cancer and infectious diseases. By harnessing the power of the body’s immune response, ImmunityBio aims to provide breakthrough treatments that can improve patient outcomes and longevity in challenging diseases.
• Lead and contribute to the design of phase I-III clinical trials including sample size calculations, interim analyses, DMC activities, and randomization procedures. • Lead and contribute to the development of clinical trial protocols and clinical study reports; write statistical methodology section of these documents. • Develop and prepare statistical analysis plans, statistical output shells, and analysis dataset specifications. • Guide and contribute to the creation, validation, traceability, reproducibility, and maintenance of the analysis datasets and statistical outputs. • Contribute to the electronic submission of clinical trial data to regulatory authorities. • Proactively solve problems of statistical complexity. • Provide input or lead data standardization efforts (e.g., CRF and database design, edit checks, standard statistical programs, data presentations, data standards such as CDISC STDM/ADaM, and e-submissions). • Participate effectively as a key member on clinical study teams. • Provides analytical insight on statistical methodology and advice to internal teams of accordingly. • Keep current with new clinical trial designs and statistical methodology. • As necessary, provide work direction, guidance, mentoring, influence and support to junior staff. • Train junior staff in more complex statistical methodology. • Create, edit and adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates. • Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities.
• Bachelors’ Degree in Statistics or Biostatistics is required with at least 7+ years of relevant experience is required; OR Masters’s Degree in Statistics or Biostatistics is required with at least 5+ years of relevant experience is required. • 3+ years of experience Biostatistician in the Biotech or Pharmaceutical industry is required. • Working knowledge of clinical research, Good Clinical Practices (GcP), and regulatory requirements/guidelines. • Proficient in SAS; familiar with sample size software such as nQuery or PASS. • Experience as a Lead Biostatistician on several concurrent projects. • CDISC STDM/ADaM experience. • Excellent English verbal and written communication skills; good organizational and interpersonal skills.
• Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day
Apply Now🕒 March 25
Managing clinical study strategies and evidence generation for regulatory approvals at Intuitive Surgical. Collaborating closely with stakeholders and leading clinical protocols execution.
🇺🇸 United States – Remote
💵 $147.6k - $212.4k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 March 17
51 - 200
Clinical Trial Manager managing phase 1-3 clinical trials at a leading biotech company. Overseeing trial operations, ensuring adherence to protocols and regulations, and coordinating with cross-functional teams.
🇺🇸 United States – Remote
💵 $150k - $172k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 March 13
Regional Clinical Trial Manager managing clinical trial operations in neurodegeneration for biopharmaceutical company. Requires strong experience in clinical research and project management.
🕒 March 6
Experienced Clinical Trial Manager overseeing site interactions and compliance with protocols in a biopharmaceutical organization. Collaborating with teams to enhance clinical trial management and patient safety across various locations.
🇺🇸 United States – Remote
💵 $114k - $210.9k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 March 1
Senior Clinical Scientist working to monitor and analyze clinical data in phases 1-3 studies for Crinetics. Collaborating with a multidisciplinary team to enhance therapies for endocrine diseases.