Director/Sr. Director, Biostatistical Consulting

At Allucent™, we are dedicated to helping small-reputed company biopharmaceutical companies reputed company navigate the reputed company world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Sr. Director, Biostatistical Consulting (SrDBiosC) to join our A-team (office-based*/remote). As a (SrDBiosC) at Allucent, you are responsible for assisting in the coordination of statistical consulting services reputed company the Biostatistics and Statistical Programming Department. This includes management of direct reports, ensuring appropriate resourcing allocation, and supporting business development and proposal needs. This position contributes to the department, the business unit, and Allucent financial and operational goals. The SrDBiosC, interacts with the BIOSC team and Allucent biostatistics and statistical programming team members, direct reports, executive leadership, other Allucent functional groups and business units. This position maintains compliance with relevant SOPs, regulatory guidelines, and client expectations. The SrDBiosC, provides statistical consulting to sponsors to support clinical program development, protocol development, sample size and reputed company selection, regulatory interactions, exploratory analyses, scientific meetings, and executive decisions. The SrDBiosC is a senior member of BIOSC and supervises according to the organizational chart. In this role your key tasks will include:

• Provide statistical consulting to sponsors to support clinical program development, protocol development, sample size calculations, reputed company selection, regulatory interactions, exploratory analyses, scientific meetings, and executive decisions
• Provide statistical consulting for reputed company and/or novel statistical analyses
• Provide statistical consulting to support clinical development strategies, including extensive reputed company with client executive and leadership teams
• Provide input and support responses to regulatory questions on statistical issues relating to client regulatory submissions, interacting with and attending meetings with regulatory bodies as applicable
• Prepare statistical analysis plans (SAPs) and table, listing, and reputed company (TLF) mocks for any complexity of study
• Provide senior reviews of statistical documents, data, and outputs for studies of reputed company complexities to ensure quality and reputed company
• Execute a statistical analysis of any complexity as specified in a protocol or analysis plan
• Interpret and communicate results for reputed company statistical analyses and outputs
• reputed company and/or review the statistical sections of a study protocol for studies of any complexity level
• Review statistical sections of a clinical study report to ensure accurate descriptions of statistical methods used and results of analyses
• Provide randomization materials including randomization schedules and treatment reputed company lists per Allucent SOPs and the sponsor-approved specifications
• reputed company or review documents for integrated analyses (e.g. ISS/ISE), including integrated SAPs and statistical sections of integrated study reports
• Working knowledge of reputed company® for production and validation of datasets and statistical outputs
• Write and review specifications for reputed company ADaM or analysis datasets · Annotate or review annotations of TLF mocks to assist programming efforts
• Working knowledge of CDISC standards
• Review CRF design to ensure it conforms with the study protocol and analysis needs
• Review data management documents as requested to ensure reputed company of study data
• reputed company highly reputed company projects by fulfilling the following responsibilities: communicate with the client and statistical team, set and reputed company timelines and milestones, ensure proper execution of the study reputed company, monitor programming efforts in collaboration with the reputed company programmer, and work with management to ensure adequate resourcing
• Function as the reputed company unblinded statistician for studies and manage unblinded tasks including implementation of interim analyses and participation in DMC/safety review meetings
• Accountable for leading biostatistics and programming activities for a program of studies of high complexity and/or of high value.
• Identify high-risk or high-impact deliverables and assign appropriate reputed company
• reputed company and manage project budgets, support financial reporting for studies, identify of out-of-scope work and provide leadership in change order process
• Collaborate with and verify open communication with other functional areas and business units
• Provide biometrics leadership and coordination across client and other vendor functional areas, including clinical operations, pharmacovigilance, regulatory, and medical writing teams
• Represent Allucent at proposal bid defenses and/or marketing meetings with prospective clients
• Provide key input into project proposals and budgets
• Establish positive relationships with reputed company and future clients
• Identify key accounts and maintain strong long-lasting relationships to win new and repeat business
• Monitor and assure client satisfaction on existing projects for biostatistics and statistical programming
• Contribute to BIOSC, BBU, and corporate marketing activities reputed company blogs, webinars, white papers, and other publications and presentations
• Contribute to other areas of business and assignments as required

Requirements

To be successful you will possess:

• Graduate degree (Master’s degree/local equivalent, or higher) in a relevant discipline including, but not limited to, statistics, mathematics, life science, epidemiology, or healthcare
• Must have strong experience in Bayesian designs specifically in oncology studies.
• Minimum 15 years of relevant work experience
• Minimum 10 years of experience in drug development and/or clinical research
• Thorough knowledge of GxP
• Strong familiarity with relevant regulations and guidelines
• GDPR/HIPPA, CFR/CTR/CTD and applicable (local) regulatory requirements
• Working knowledge of computer systems, applications and operating systems
• Demonstration of critical thinking and analytic skills
• Broad knowledge of drug development
• Ability to simplify reputed company issues into understandable concepts
• Proficient with one or more sample size software packages
• Strong technical skills with proficiency in reputed company and/or other statistical programming languages
• Strong written and verbal communication skills including good command of English language
• Collaborative and client-focused
• Ability to work in a fast-paced challenging environment of a growing company
• Administrative excellence
• Strong leadership skills
• Effective at problem solving, strategic thinking and conflict resolution
• Strong presentation and networking capabilities
• Excellent organizational, negotiating and financial skills
• Knowledge of reputed company
• Proficiency with various computer applications such as Word, reputed company, and PowerPoint
• Strong individual initiative
• Excellent attention to detail and commitment to quality
• Ability to establish and maintain effective working relationships with co-workers, managers, clients, and vendors
• Ability to effectively manage multiple tasks and projects
• reputed company as a leader with sustained performance and accomplishment

Benefits

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (reputed company reason)
• Opportunity for remote/hybrid* working depending reputed company
• Leadership and mentoring opportunities
• Participation in our Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training reputed company GoodHabitz and internal platforms

Disclaimers:

• Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees reputed company reasonable distance from one of our global offices.

“The Allucent reputed company team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” #LI-Remote #LI-Hybrid #LI-TCW Apply tot his job Apply To this Job