Job
Description
As a Biostatistician at our rapidly growing company, you will be an integral part of the Biometrics team based in Pune. Your role will involve contributing to the clinical development plan, reviewing study protocols, preparing statistical methodologies, and developing detailed Medpace Data Analysis Plans for assigned projects. You will also be responsible for programming study analysis, reviewing study results, and preparing the statistical methods section for clinical/statistical reports. In addition, you will communicate project requirements for CRF design, database design, and database cleanup to ensure key study variables are suitable for analysis. Furthermore, you will communicate statistical results to medical writing personnel to ensure accurate interpretation. Qualifications: - Ph.D. degree in Biostatistics/Statistics with pharmaceutical clinical trial experience - 10+ years' industry experience in Clinical Trial or equivalent - Strong experience in SAS programming or equivalent - Knowledge of other statistical software and advanced statistical methods - Knowledge of the pharmaceutical industry and regulatory requirements/guidelines for drug development - Familiarity with complex statistical methods applicable to Phase I-IV clinical trials - Experience in generating analysis databases and analyses for medium to high complexity clinical trial projects including ISS, ISE, and electronic submissions - Excellent verbal and written communication skills As a full-service clinical contract research organization (CRO), Medpace provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and over 5,000 employees across 40+ countries, we leverage local regulatory and therapeutic expertise in key areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. At Medpace, you can expect: - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards: - Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024 - Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility Next Steps: A Medpace team member will review your qualifications, and if interested, you will be contacted with details for the next steps. As a Biostatistician at our rapidly growing company, you will be an integral part of the Biometrics team based in Pune. Your role will involve contributing to the clinical development plan, reviewing study protocols, preparing statistical methodologies, and developing detailed Medpace Data Analysis Plans for assigned projects. You will also be responsible for programming study analysis, reviewing study results, and preparing the statistical methods section for clinical/statistical reports. In addition, you will communicate project requirements for CRF design, database design, and database cleanup to ensure key study variables are suitable for analysis. Furthermore, you will communicate statistical results to medical writing personnel to ensure accurate interpretation. Qualifications: - Ph.D. degree in Biostatistics/Statistics with pharmaceutical clinical trial experience - 10+ years' industry experience in Clinical Trial or equivalent - Strong experience in SAS programming or equivalent - Knowledge of other statistical software and advanced statistical methods - Knowledge of the pharmaceutical industry and regulatory requirements/guidelines for drug development - Familiarity with complex statistical methods applicable to Phase I-IV clinical trials - Experience in generating analysis databases and analyses for medium to high complexity clinical trial projects including ISS, ISE, and electronic submissions - Excellent verbal and written communication skills As a full-service clinical contract research organization (CRO), Medpace provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and over 5,000 employees across 40+ countries, we leverage local regulatory and therapeutic expertise in key areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. At Medpace, you can expect: - Flexible work environment - Competitive compensation and benefits package
