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Senior Statistician

VirtualVocations

Pasadena (CA)

Remote

USD 90,000 - 120,000

Full time

Today
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Job summary

A leading company is seeking a Study Lead Statistician to oversee statistical activities for clinical studies. The role involves guiding statistical methodologies, collaborating with teams, and ensuring compliance with regulatory standards. Ideal candidates should have a strong background in statistics and experience in the pharmaceutical industry.

Benefits

Medical & pharmacy coverage
Dental / vision insurance
401(k)
Health saving account (HSA)
Flexible spending account (FSA)
Life Insurance
Pet Insurance
Short term and Long term Disability
Employee Assistance Program (EAP)

Qualifications

  • At least 4 years of statistical experience in the pharmaceutical industry.
  • Strong skill in communicating statistical information clearly.

Responsibilities

  • Lead statistical activities of clinical studies.
  • Provide statistical guidance and review protocols.
  • Collaborate with cross-functional teams for study deliverables.

Skills

Statistical Analysis
Communication
Leadership
Statistical Methodologies
R Programming
SAS Programming

Education

Masters degree in Statistics
PhD in Statistics

Job description

Innova Solutions has a client that is immediately hiring for Study Lead Statistician - Product Facing

Position type : Full Time Contract

Duration : 12 months Contract

Location : Remote

As Study Lead Statistician - Product Facing, you will :

Key Responsibilities

The Study Lead Statistician (SLS) for product facing work is responsible for leading statistical activities of clinical studies. The SLS works closely with cross-functional team members to ensure their clinical studies are appropriately planned, have the required statistical power for success, comply with Regulatory requirements and standards, and maintain statistical, as well as operational, integrity throughout the life of the study. The SLS works closely with the Global Statistical Lead to ensure their study aligns with the overall product strategy. The SLS also works closely with the Study Statistician, who performs all the operational activities related to the statistics-related deliverables. The SLS is responsible for the integrity and quality of their study. The SLS also supports product level activities that could include Regulatory activities as well as publication work.Core Responsibilities : Provide statistical guidance, review, and contribution to protocols, SAPs; TFL shells; DMC Charters; SDF specifications (SDTM and ADaM); randomization specifications; other key-study related documentation, protocol deviations, data quality review, and other communications Attend and be a contributor at Clinical Study Team Meetings Attend meetings for and provide statistical input into cross-functional study start-up activities, including but not limited to CRF development, database specifications review, database development, IVRS specification review Initiate cross-functional team meetings as necessary (e.g., SAP review, TFL shell review, TFL review) Provide statistical guidance, review, and be responsible for statistical analysis of individual studies / projects Perform and document QC of primary and key secondary endpoints within ADaM datasets as well as the statistical analyses of these endpoints (programmatically) Perform data-driven modeling during clinical studies Coordinate the creation of required outputs for Dose Level Review Meetings (DLRMs) as well as coordinate and participate in the DLRM Review TFLs created by statistical programming for consistency and accuracy Author analysis reports such as Flash Memo, and results section of the CSRs Collaborate with the study programming team for study deliverables Manage timelines for all statistics-related deliverables by working with the cross-functional team members (e.g., programmers, study statisticians, clinical data managers, medical writers) Be familiar with all Companys policies, SOPs and other controlled documents related to study activities noted above Assist with study and systems audits conducted by Company GCA and external bodies

Minimum Education Required : Masters degree in Statistics / Biostatistics or other subject with high statistical content with at least 4 years of post-graduate statistical experience in the pharmaceutical industry or medical research (or PhD degree with at least 3 years experience) Strong skill in communicating statistical information clearly and concisely (written and oral) Strong understanding of statistical concepts related to the design and conduct of clinical studies Strong ability to apply statistical methodologies in the analysis of clinical trials Independent leadership of the design, analysis and reporting of at least 1 complex or multiple less complex studies / projects within the Pharmaceutical / Biotechnology / Public Health setting in Industry, Government or Academia Previous experience in the development, author, and execution of protocols and SAPs, as well as review of CSRs Excellent oral and written English communication skills Strong SAS and / or R programming skills in conducting simulations and applying statistical concepts and methods based on complex study designs

Preferred Qualifications : Masters degree in Statistics / Biostatistics or other subject with high statistical content and at least 6 years of post-graduate statistical experience in the pharmaceutical industry or medical research OR Doctoral degree in Statistics / Biostatistics or other subject with high statistical content and 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research Designing, analyzing and reporting of clinical trials within Pharmaceutical / Biotechnology / Public Health setting in Industry, Government or Academia Demonstrated ability in presenting results and defending statistical findings, study design and analysis to internal audiences (study / product team) AND at external meetings such as investigator meetings, steering committee meetings, ad board meetings or regulatory meetings Leadership of at least 3 clinical studies / projects end-to-end with minimal oversight Life Cycle Drug Development Experience (Pre-clinical Development, Clinical Development, and Post-marketing) Experience in adaptive clinical trials and innovative study designs Experience in the utilization of Bayesian statistics in clinical trials Proficient R programming skills conducting simulations and applying statistical concepts and methods based on complex study designs

  • Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc.

Benefits : Innova Solutions offers benefits( based on eligibility) that include the following : Medical & pharmacy coverage, Dental / vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP).

ABOUT INNOVA SOLUTIONS : Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields.

Recent Recognitions :

  • Named One of America’s Best Employers for New Grads by Forbes (2024
  • Named One of the Best Companies to Work For by U.S. News & World Report (Private Companies List, 2024-2025)
  • One of the Largest IT Staffing Firms in the US – Ranked #3 by Staffing Industry Analysts (SIA, 2024)
  • One of the Largest Staffing Firms in the US – Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics)
  • Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023)
  • One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024)
  • AWS Advanced Tier Services Partner with 100+ certifications

Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at [emailprotected] or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics / Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b.

The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws

Benefits : Innova Solutions offers benefits( based on eligibility) that include the following : Medical & pharmacy coverage, Dental / vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP).

ABOUT INNOVA SOLUTIONS : Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields.

Recent Recognitions :

  • One of Largest IT Consulting Staffing firms in the USA – Recognized as #4 by Staffing Industry Analysts (SIA 2022)
  • ClearlyRated Client Diamond Award Winner (2020)
  • One of the Largest Certified MBE Companies in the NMSDC Network (2022)
  • Advanced Tier Services partner with AWS and Gold with MS

Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please call (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics / Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b.

The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

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