Sr Biostatistician (Immunology)

Syneos Health Commercial Solutions

15d ago

Job
Full-time
Junior, Mid & Senior Level
Science
Research & Development
Madrid

AI generated summary

You need a graduate degree in biostatistics, extensive clinical trial experience, programming skills, and strong communication abilities, plus regulatory submission experience is preferred.
You will mentor biostatisticians, direct project activities, prepare SAPs and analysis datasets, ensure quality control, support clients, and manage timelines for various projects.

Requirements

Graduate degree in biostatistics or related discipline.
Extensive experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies.
Proficiency in programming.
Ability to apply extensive knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research and to effectively communicate statistical concepts.
Experience across all statistical tasks required to support clinical trials during the lifecycle of the project, from protocol to CSR.
Experience with regulatory submissions preferred.
Excellent written and verbal communication skills.
Ability to read, write, speak, and understand English.

Responsibilities

Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Conducts training sessions, or otherwise trains new hires and enhance the skills of existing personnel.
Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department.
Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR.
Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborates with sponsor, if required.
May be responsible as Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report.
Creates or reviews programming specifications for analysis datasets, tables, listings, and figures.
Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis.
Implements company objectives, and creates alternative solutions to address business and operational challenges.
As biostatistics representative on project teams, interfaces with other departmental project team representatives.
Preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others.
Conducts and participates in verification and quality control of project deliverables, ensuring that output meets the expected results and is consistent with analysis described in the SAP and specifications.
May lead complex or multiple projects (e.g. submissions, integrated analyses), and attend regulatory agency meetings or responds to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor.
Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, discusses time estimates for completion of study related activities with biostatistics management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines.
Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalates to management.
Provides statistical programming support as needed.
May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities, including charter development and serving as an independent non-voting biostatistician. May serve as a voting statistician on DSMBs and/or DMCs.
Provides input and reviews, and subsequently follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs; ensuring inspection readiness.
Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business.
Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings.
Performs other work-related duties as assigned.
Minimal travel may be required.

FAQs

What is the job title for this position?

The job title is Sr Biostatistician (Immunology).

What qualifications are required for this role?

A graduate degree in biostatistics or a related discipline is required, along with extensive experience in clinical trials.

Is immunology experience essential for this position?

No, immunology experience is not essential.

What programming skills are needed for this position?

Excellent R skills are essential, and SAS is nice to have.

What are the expected years of experience for candidates?

Candidates should have 2-6 years of experience from graduation.

Is knowledge of the Estimands framework required?

Yes, knowledge of the Estimands framework is required.

Where is this position based?

The position is targeting candidates in the East or Central Time Zones in the US, with a preference for candidates in Europe who have less than 3 months notice.

Does this job involve mentoring other biostatisticians?

Yes, the Sr Biostatistician will mentor biostatisticians on job skills and oversee or develop training plans.

Will there be opportunities for professional development?

Yes, Syneos Health is passionate about developing its people through career development and progression.

Are there travel requirements for this position?

Minimal travel may be required.

What is the salary range for this position?

The annual base salary for this position ranges from $95,000 to $175,700.

What benefits are offered for this position?

Benefits may include a company car or car allowance, health benefits, 401k match, participation in the Employee Stock Purchase Plan, commissions/bonus potential, and flexible paid time off (PTO) and sick time.

Does this position support remote work?

Yes, remote work is supported but in a hybrid format.

Is prior experience with regulatory submissions preferred for this role?

Yes, experience with regulatory submissions is preferred.

Syneos Health Commercial Solutions

Science & Healthcare

Industry

10,001+

Employees

Mission & Purpose

Syneos Health® (Nasdaq:SYNH) is the only fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. We bring together a talented team of professionals, who work across more than 110 countries, with a deep understanding of patient and physician behaviors and market dynamics. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.