Authoring statistical sections of reports, and contributing to concept protocols, protocols, case report forms and integrated clinical/statistical reports. Primary authorship and responsibility for analysis plans and statistical reports. Primary responsibility and/or accountability for the statistical analyses, tabulations, graphics and listings of clinical trial data. Ability to coordinate and delegate the production of data displays in an efficient manner for inclusion in integrated clinical/statistical reports and other similar reports. Ensuring statistical and integrated clinical/statistical reports meet regulatory and company standards. Perform quality assurance procedures on work performed by others. Performs, presents and interprets data manipulations/processing and statistical analyses. Derives statistical conclusions and makes recommendations based on experimental results. Liaise with customers to understand and help define requirements. Represent Biometrics at Investigator Meetings, internal teams, contract organizations and external regulatory agencies.

Required Skills:  PhD in Biostatistics or related field. Broad understanding of statistical methods within context of clinical trials. Broad knowledge of SAS and Unix. Proven ability to organize workload and priorities and complete tasks on time. Demonstrated ability to work effectively in a team environment. Strong interpersonal skills and ability to communicate effectively.  Ability to complete tasks under limited supervision. 

Phase I-Clinical Pharmacology experience in the therapeutic area of Oncology

Experience Level:  Minimum of 2 years related experiences within the Contract Research Organization (CRO) or pharmaceutical/clinical trials environment

To apply: Please email hprice@clinforce.com or call 800.964.2877 ext 33826

ClinForce provides talented clinical research and data science professionals with exciting and rewarding career opportunities. Pharmaceutical, biotechnology, device, CRO and related clinical research organizations trust ClinForce with their outsourced project needs, contract staffing requirements and direct hire objectives. For more than two decades, we have focused our energies exclusively on the clinical trials industry, building a reputation of excellence among the world's leading R&D organizations. These organizations have come to depend on our strength. With an extensive network of talented, experienced clinical research and data science professionals and a seasoned recruiting team, ClinForce is capable of introducing the brightest and most experienced profesionals to companies seeking clinical research and data science expertise.