Updated:
January 29, 2025 Location:
Europe-United Kingdom Job ID:
25001523 *US: Targeting someone in East or Central Time Zone (No West Coast) *Europe: Preferred: Targeting someone with less than 3 months notice Syneos Health is a leading 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. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job responsibilities Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality work. 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. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Implements company objectives, and creates alternative solutions to address business and operational challenges. Conducts and participates in verification and quality control of project deliverables. May lead complex or multiple projects and attend regulatory agency meetings or respond to questions as needed. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities. Qualifications Senior Level (2-6 years’ experience from graduation) PhD, Strong MSc Excellent R skills essential, SAS nice to have Experience working on submissions Clinical Trial knowledge SDTM, ADaM experience Knowledge of Estimands framework Immunology experience not essential What we’re looking for Graduate degree in biostatistics or related discipline. Extensive experience in clinical trials or an equivalent combination of education and experience. Proficiency in programming. Ability to apply extensive knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against.
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January 29, 2025 Location:
Europe-United Kingdom Job ID:
25001523 *US: Targeting someone in East or Central Time Zone (No West Coast) *Europe: Preferred: Targeting someone with less than 3 months notice Syneos Health is a leading 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. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job responsibilities Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality work. 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. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Implements company objectives, and creates alternative solutions to address business and operational challenges. Conducts and participates in verification and quality control of project deliverables. May lead complex or multiple projects and attend regulatory agency meetings or respond to questions as needed. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities. Qualifications Senior Level (2-6 years’ experience from graduation) PhD, Strong MSc Excellent R skills essential, SAS nice to have Experience working on submissions Clinical Trial knowledge SDTM, ADaM experience Knowledge of Estimands framework Immunology experience not essential What we’re looking for Graduate degree in biostatistics or related discipline. Extensive experience in clinical trials or an equivalent combination of education and experience. Proficiency in programming. Ability to apply extensive knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against.
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