Principal Biostatistician managing clinical trials and statistical analyses for ICON plc. Lead biostatistical efforts in drug development across multiple sponsors focusing on Vaccines, Oncology, and Rare Diseases.
Responsibilities
Serves as lead biostatistician for programs of studies, submissions, or on simple to complex individual studies.
Oversees statistical activities that support ICON’s interactions with clients and regulatory agencies.
Reviews and approves statistical methods sections of study protocols, statistical analysis plans and statistical input to reports.
Prepares and approves research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients.
Participates in bid defense meetings and makes presentations at marketing meetings with prospective clients.
Requirements
Master's degree or PhD in Biostatistics, Statistics, or a related field
9 or more years of biostatistical experience with Master’s degree; 7 or more years required with PhD
Advanced Knowledge of multiple statistical and therapeutic areas, the drug development process, and statistical programming practices and procedures.
Advanced ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical studies.
Effective written and oral communication skills with demonstrated leadership ability.
Benefits
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Clinical Research Coordinator IV managing complex clinical trials and supervising research administration staff. Handling compliance, budgets, and participant engagement strategies in a healthcare setting.
Senior Biostatistician providing statistical contributions and leading strategies for clinical trials and regulatory submissions. Ensuring quality deliverables and interacting with regulatory authorities.
Clinical Research Leader managing clinical trials for J&J MedTech Neurovascular in Irvine, CA. Oversee study execution, compliance, and team collaboration for innovative treatment solutions.
Clinical Research Leader managing clinical trials within the Neurovascular team at Johnson & Johnson. Leading projects ensuring compliance with regulations and fostering relationships across departments.
Senior Manager overseeing clinical research operations including study operations and trial management. Seeking experienced leader for a prominent position at Mission Hospital.
Clinical Research Coordinator responsible for clinical trial oversight at Thomas Jefferson University. Ensuring compliance with regulations and managing daily clinical research operations.
Clinical Research Coordinator responsible for coordinating clinical trials and ensuring regulatory compliance. Conducting patient care activities and maintaining data integrity in accordance with study protocols.
Clinical Research Coordinator managing significant aspects of clinical trials in the School of Medicine. Overseeing data management and training less experienced staff under Emory University.
Clinical Research Coordinator II managing research project databases and guiding staff at Emory University. Ensuring compliance with protocols and handling participant recruitment and data collection.