Senior Biostatistician – Global BIOS
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Senior Biostatistician providing statistical consulting and technical support for clinical trial studies. Collaborating with teams on global projects and managing complex study budgets and proposals.
Responsibilities:
- Provide statistical consulting and technical support related to the design, statistical analysis, and regulatory submissions of clinical trial studies
- Act as a statistical team lead for single, complex studies or groups of studies
- Manage the scope of work and budget, providing revenue and resource forecasts
- Prepare proposal text and attend bid defense meetings
- Collaborate with medical and programming staff to produce interim and final reports of clinical trial data
Requirements:
- BSc or MSc degree in Biostatistics or related field
- Between 4 - 6 years’ relevant experience
- Familiarity with moderately complex statistical methods that apply to applicable clinical trials
- Good working knowledge of SAS and CDISC SDTM and ADaM
- Ability to effectively manage multiple tasks and project
- Ability to communicate and explain statistics
Benefits:
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge and innovative, in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance, with a strong focus on a positive well-being
Similar Jobs
Director, Clinical Research
Director of Clinical Research at Sumitomo Pharma leading planning and execution of clinical development programs. Overseeing clinical study integrity and relationships with stakeholders in various indications.
Clinical Research Program Navigator
Clinical Research Program Navigator at City of Hope guiding cancer patients and families through clinical trials. Collaborating with clinical teams to enhance patient experience and care coordination.
Clinical Scientist
Clinical Scientist supporting design and execution of real-world evidence research studies at Heart Rhythm Clinical Research Solutions. Collaborating with multidisciplinary teams to translate findings into clinical advancements.
Clinical Trial Manager
Clinical Trial Manager overseeing project deliverables in Israel for Syneos Health. Engaging with local study teams and managing site operations and stakeholder communications.
Clinical Scientist
Clinical Scientist at Catalyst Clinical Research assessing clinical data integrity and collaborating with teams. Mainly responsible for reviewing trends and findings of clinical data.
Associate Clinical Trial Manager
Associate Clinical Trial Manager supporting clinical trial activities for a leading biotechnology company. Coordinating trial operations and ensuring compliance in clinical studies.
Clinical Trial Specialist
Senior Site Management Associate ensuring compliance and data quality in clinical trials for ICON. Overseeing site management activities and mentoring junior staff for effective collaboration.
Associate Director, Clinical Scientist – Late Development, Obesity Therapeutic Area
Clinical Scientist Associate Director supporting late-phase clinical development with a focus on data quality at Amgen. Collaborating on clinical trials and ensuring high-quality clinical data results.
Clinical Scientist Director – Cardiovascular Trials
Clinical Scientist Director managing cardiovascular trials for Amgen. Supporting execution and quality delivery of global late-stage clinical studies in cardiovascular research.
Clinical Scientist, Clinical Science
Clinical Scientist responsible for administering assessments in clinical trials for mental health. Evaluating rater performance and ensuring reliable data collection in Latin America.
Senior Scientist – Clinical Research
Senior Scientist Clinical Research for Abbott Nutrition translating complex scientific research into product claims and educational content. Collaborating with stakeholders to ensure scientific excellence across the product portfolio.
Director, Clinical Scientist – Respiratory Indications
Director, Clinical Scientist leading respiratory clinical development at Generate Biomedicines. Focused on asthma and COPD studies, driving protocol development, data analysis, and regulatory documentation.
Principal Biostatistician – Chemistry, Manufacture and Control (CMC)
Principal CMC Biostatistician providing statistical support across pharmaceutical manufacturing processes. Strong focus on analytics, regulatory compliance, and collaboration with interdisciplinary teams.
Clinical Trial Manager, Senior Clinical Trial Manager
Project Manager at ICON plc overseeing clinical trial projects, ensuring delivery on time and within budget. Leading cross-functional teams and engaging with stakeholders across project execution.
Associate Director – Biostatistician
Associate Director/Director Biostatistician providing strategic leadership for clinical trials at ClinChoice. Engaging in statistical activities across multiple studies in a global CRO environment.
Senior Clinical Scientist
Senior Clinical Scientist supporting clinical trials and data services at Cogstate. Focusing on computerized testing and cognitive assessments.
Clinical Scientist Associate Director – Autoimmune/Inflammation
Clinical Scientist Associate Director supporting late-phase clinical development at Amgen. Contributing to protocol development, data review, and cross-functional team collaboration.
Clinical Scientist Director – Late Development, Rare Disease
Clinical Scientist Director managing late-phase clinical development at Amgen. Supporting scientific and clinical strategy translation into actionable execution across clinical trials.
Regional Clinical Trial Manager
Regional Clinical Trial Manager managing clinical trial operations in neurodegeneration for biopharmaceutical company. Requires strong experience in clinical research and project management.
Clinical Trial Manager – FSP
Clinical Trial Manager managing external vendors and overseeing clinical trial execution for Parexel. Ensuring adherence to GCPs and leading study material design and documentation.