Responsibilities May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. Provides expert consultation to projects across the company on statistical methodology. Solves problems of complex statistical scope. Provides technical review of proposed statistical design for research studies across company. Serves as the lead Biostatistician on one or more study projects. Participates in statistical process development and improvement across company. May present at statistical conferences. Provides sound strategic, scientific and statistical input to support client’s research projects. Leads the project team’s development of study analysis plans and statistical programs to perform analyses and display study data. Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted. Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices. Ensures the scientific integrity of the research project and the accuracy of the reported results. Performs sample size calculation and provides leadership in the statistical design of research projects. Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained. Develops study assignment allocation schemas along with appropriate documentation. Leads the development of the methods and results sections of clinical study reports and scientific publications. Represents Client on behalf of clients at regulatory meetings. Provides expertise in methodological advances both internally and externally to improve statistical methodologies. Participate in the development and updating of Standard Operating Procedures. Other duties as assigned Qualifications MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required. Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development. Demonstrated proficiency with statistical methods and applications in clinical research. Strong programming skills in SAS and/or R. Expertise in state-of-the-art data manipulation and statistical methodology. Excellent communication, interpersonal and organization skills. Ability to manage multiple tasks. Ability to work independently, as well as in a team environment. Ability to effectively communicate complex statistical concepts, both written and oral.
Responsibilities May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. Provides expert consultation to projects across the company on statistical methodology. Solves problems of complex statistical scope. Provides technical review of proposed statistical design for research studies across company. Serves as the lead Biostatistician on one or more study projects. Participates in statistical process development and improvement across company. May present at statistical conferences. Provides sound strategic, scientific and statistical input to support client's research projects. Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data. Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted. Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices. Ensures the scientific integrity of the research project and the accuracy of the reported results. Performs sample size calculation and provides leadership in the statistical design of research projects. Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained. Develops study assignment allocation schemas along with appropriate documentation. Leads the development of the methods and results sections of clinical study reports and scientific publications. Represents Client on behalf of clients at regulatory meetings. Provides expertise in methodological advances both internally and externally to improve statistical methodologies. Participate in the development and updating of Standard Operating Procedures. Other duties as assigned Qualifications MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required. Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development. Demonstrated proficiency with statistical methods and applications in clinical research. Strong programming skills in SAS and/or R. Expertise in state-of-the-art data manipulation and statistical methodology. Excellent communication, interpersonal and organization skills. Ability to manage multiple tasks. Ability to work independently, as well as in a team environment. Ability to effectively communicate complex statistical concepts, both written and oral.
Job Title: Entry-Level Life Sciences Recruiter Location: Hyderabad Type: Full-Time Job Description: We are seeking an enthusiastic Entry-Level Life Sciences Recruiter to join our team. In this role, you will source, screen, and engage candidates for positions in the pharmaceutical, biotech, and healthcare industries. You will learn full-cycle recruiting, build relationships with candidates, and support client hiring needs. Qualifications: Recent graduates. Strong communication and interpersonal skills. Eagerness to learn recruiting and staffing processes. What We Offer: Comprehensive training and mentorship. Career growth opportunities in life sciences staffing. Dynamic and supportive team environment.
Title: Senior Biostatistician Location: Remote/ Bangalore, India Contract: 3 Months Primary Purpose Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies. Responsibilities May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. Provides expert consultation to projects across the company on statistical methodology. Solves problems of complex statistical scope. Provides technical review of proposed statistical design for research studies across company. Serves as the lead Biostatistician on one or more study projects. Participates in statistical process development and improvement across company. May present at statistical conferences. Provides sound strategic, scientific and statistical input to support client’s research projects. Leads the project team’s development of study analysis plans and statistical programs to perform analyses and display study data. Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted. Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices. Ensures the scientific integrity of the research project and the accuracy of the reported results. Performs sample size calculation and provides leadership in the statistical design of research projects. Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained. Develops study assignment allocation schemas along with appropriate documentation. Leads the development of the methods and results sections of clinical study reports and scientific publications. Represents EMMES on behalf of clients at regulatory meetings. Provides expertise in methodological advances both internally and externally to improve statistical methodologies. Participate in the development and updating of Standard Operating Procedures. Qualifications MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required. Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development. Demonstrated proficiency with statistical methods and applications in clinical research. Strong programming skills in SAS and/or R. Expertise in state-of-the-art data manipulation and statistical methodology. Excellent communication, interpersonal and organization skills. Ability to manage multiple tasks. Ability to work independently, as well as in a team environment. Ability to effectively communicate complex statistical concepts, both written and oral
**This is a Contract job for 3 months with possible extensions** Primary Purpose The Senior Statistical Programmer provides lead statistical programming support for multiple clinical projects using SAS and provides expert consultation across the company. Key responsibilities include delivering key regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff. The role also includes providing project updates to management while performing assigned duties and presents internally on statistical programming topics. Responsibilities Provides lead statistical programming support for multiple clinical research study projects or study teams. Provides statistical programming development with SAS (Base and Macros) and provides expert consultation to projects across the company including statistical programming methodology. Ensures that sound methodologies are adopted by establishing proficiency of programming techniques required for clinical trials research which involve either CDISC standards and analysis data sets or production of standard and custom tables listings and figures. Provides key deliverables based on established profiency of regulatory requirements for clinical research E-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings. Develops programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and may contribute to standardization efforts. Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed. Keep abreast of current statistical programming techniques to ensure the adoption of sound methodologies. Presents statistical programming topics internally and may present at external conferences. Provides project updates to appropriate project management or department management staff. Qualifications A bachelor's degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred. Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, and ICH guidance and recommendations) in Clinical Research. Good analytical skills with the ability to process scientific and medical data. Strong skills in prioritization, problem-solving, organization, decision-making, and time management. Ability to articulate complex programming and technical concepts through written and oral communication. Strong statistical programming skills in SAS, familiarity with R, Python or other relevant statistical software considered beneficial.