Experienced Biostatistician

Contribute to clinical development plan preparation; Review of study protocol and preparation of statistical methodologies; Development of detailed Medpace Data Analysis Plan for assigned projects; Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports; Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and Communicate statistical results to medical writing personnel to ensure accurate interpretation. Our global activities are growing rapidly, and we are currently seeking a full-time, Hyderabad-based Biostatistician to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Contribute to clinical development plan preparation; Review of study protocol and preparation of statistical methodologies; Development of detailed Medpace Data Analysis Plan for assigned projects; Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports; Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and Communicate statistical results to medical writing personnel to ensure accurate interpretation. Qualifications Ph.D. degree in Biostatistics/Statistics with pharmaceutical clinical trial experience; Strong experience in SAS programming or equivalent; Knowledge of other statistical software; of advanced statistical methods and knowledge of the pharmaceutical industry; Knowledge of regulatory requirements/guidelines for drug development; Familiarity with complex statistical methods that apply to Phase I-IV clinical trials; Experience in generation of analysis databases, and analyses for medium to high complexity clinical trial projects including ISS, ISE, and electronic submissions; Excellent verbal and written communication skills Medpace Overview Why MedpacePeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Hybrid work-from-home options (dependent upon position and level) Competitive PTO packages Company-sponsored employee appreciation events Employee health and wellness initiatives Flexible work schedule Competitive compensation and benefits package Structured career paths with opportunities for professional growth Awards Recognized by Forbes as one of Americas 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 What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets