AmbitionBox
Search
Jobs
- Reviews
- Salaries
- Interview Questions
- About Company
- Benefits
- Jobs
- Office Photos
- Community
Add office photos
All Filters
47 Syneos Health Jobs
Senior Biostatistician(Oncology experience is preferred)
4-8 years
Kolkata, Mumbai, New Delhi + 4 more
1 vacancy
Senior Biostatistician(Oncology experience is preferred)
Syneos Health
posted 1mon ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
Description
Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.
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
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
- Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR.
- Prepares Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborate with the sponsor, if required.
- May be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report.
- Coordinates the activities of other biostatistics and statistical programming 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.
- 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.
- Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications.
- Implements company objectives, and create alternative solutions to address business and operational challenges.
- Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others.
- Manages scheduling and time constraints across multiple projects, sets goals based on priorities from 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 escalate to management.
- Provides statistical programming support as needed.
- May participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development and serving as an independent non-voting biostatistician.
- May lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor.
- 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.
- Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings.
- Coaches and mentors other Biostatistics staff.
- Performs other work-related duties as assigned.
- Minimal travel may be required.
Qualifications
- Ph.D is required with Oncology experienced is required.
- Min 5 years of relevant experience as Statistician in clinical trials environment working on Late phase studies and preferably 1 year as study lead.
- Good proficiency in programming.
- Ability to apply 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.
- Excellent written and verbal communication skills.
- Ability to read, write, speak, and understand English.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health .
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. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Employment Type: Full Time, Permanent
Read full job descriptionPrepare for Biostatistician roles with real interview advice
What people at Syneos Health are saying
Biostatistician salary at Syneos Health
reported by
6
employees
with 4-7
years exp.
₹1.2
L/yr - ₹23.5
L/yr
109%
more
than the average Biostatistician Salary in India
View more details
What Syneos Health employees are saying about work life
based on 589 employees
Flexible timing
Monday to Friday
No travel
Day Shift
Syneos Health Benefits
Submitted by Company
Financial Health Learning, Development and Growth Physical Health Employee Resources
Submitted by Employees
View more benefits 
Compare Syneos Health with
IQVIA
Compare
Parexel International
Compare
ICON Plc
Compare
Fortrea Development India Private Limited
Compare
WuXi AppTec
Compare
Syngene International
Compare
Aragen Life Sciences
Compare
SAI Life Sciences
Compare
Lambda Therapeutic Research
Compare
Reliance Life Sciences
Compare
Aizant Drug Research Solutions
Compare
Veeda Clinical Research
Compare
Equinox Labs
Compare
Rubicon Research
Compare
Cliantha Research
Compare
Accutest Research Laboratories
Compare
Navitas Life Sciences
Compare
Raptim Research
Compare
Axis Clinicals
Compare
Spc Life Sciences
Compare
Senior Biostatistician(Oncology experience is preferred)
4-8 Yrs
Kolkata, Mumbai, New Delhi +4 more
Senior/Principal Statistical Programmer TEAL module devlop. R/R Shiny
4-9 Yrs
India
Prin Clin Trial Reg Affairs (APAC Market )
3-7 Yrs
Kolkata, Mumbai, New Delhi +4 more
Share an Interview