PRA Health Sciences, with a location in Blue Bell, provides clinical development services including drug development and regulatory strategy plans, phase I clinical trials, phase II through IV multi-center clinical trials, development and analysis of integrated global clinical databases, and more.
Clinical Supplies Planner
This position manages clinical supply planning and forecasting for study protocols; interprets relevant protocol information to develop packaging/labeling design and/or global distribution strategy; and coordinates the origination, proofing, and translation of clinical study labels.
The ideal candidate will possess a bachelor’s degree and one year of experience in a pharmaceutical, biotech, and clinical supply logistics environment; working knowledge of the clinical trial supply process; and knowledge of project management and clinical customer relationship building.
Click here to read more about the Clinical Supplies Planner position at PRA Health Sciences.
This position serves as the lead biostatistician on project teams for simple to moderate clinical studies; develops statistical analysis plans and interprets results; contributes to clinical study protocols and clinical study reports; and participates in bid defense meetings.
The ideal candidate will possess a master’s degree in statistics, biostatistics, or a related discipline; a minimum of three years of relevant biostatistical experience; excellent communication and leadership skills; and the ability to plan, supervise, implement, and monitor statistical processes.
Click here to read more about the Biostatistician II position at PRA Health Sciences.
Site Management Associate – Real World Solutions
This position performs investigative site recruitment and feasibility analysis; and conducts document collection and review, clinical status tracking, in-house site management, and data review activities in accordance with study protocol, client and company SOPs, and all applicable regulatory requirements.
The ideal candidate will possess a bachelor’s degree in a clinical, science, or health-related discipline; a minimum of one year of clinical trials support, data coordination, or pharmaceutical industry experience; and experience communicating with sponsors, vendors, CROs, IRBs, and sites.
Click here to read more about the Site Management Associate position at PRA Health Sciences.