Job Summary:
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.
This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you.
Responsibilities: Contribute to clinical development of plan preparation; Review of study protocol and preparation of statistical methodologies; Development of detailed 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 clean-up to ensure the key study variables are suitable for analysis; Communicate statistical results to medical writing personnel to ensure accurate interpretation. Qualifications: Ph.D. degree in Biostatistics / Statistics / Medical Statistics; Experience in SAS Programming; Knowledge of advanced statistical methods and knowledge of the pharmaceutical industry; Knowledge of regulatory requirements/guidelines for drug development; Previous experience in a pharmaceutical or CRO preferred. Medpace Overview: Medpace is a full-service clinical contract research organisation (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace? People. 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: 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 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 #J-18808-Ljbffr
Responsibilities: Contribute to clinical development of plan preparation; Review of study protocol and preparation of statistical methodologies; Development of detailed 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 clean-up to ensure the key study variables are suitable for analysis; Communicate statistical results to medical writing personnel to ensure accurate interpretation. Qualifications: Ph.D. degree in Biostatistics / Statistics / Medical Statistics; Experience in SAS Programming; Knowledge of advanced statistical methods and knowledge of the pharmaceutical industry; Knowledge of regulatory requirements/guidelines for drug development; Previous experience in a pharmaceutical or CRO preferred. Medpace Overview: Medpace is a full-service clinical contract research organisation (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace? People. 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: 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 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 #J-18808-Ljbffr
