Plymouth Meeting’s Inovio Pharmaceuticals is engaged in the development of a new generation of vaccines, called synthetic vaccines, focused on cancers and infectious diseases. Its clinical programs include cervical dysplasia (therapeutic), avian influenza (preventive), prostate cancer (therapeutic), leukemia (therapeutic), hepatitis C virus (HCV), and HIV vaccines.

Clinical Programmer

This position provides programming support for clinical development programs. He/she will collaborate with the biostatistics and data management divisions to provide programming for data summaries, statistical analyses, tables, listings, and figures. The person will maintain standards and best practices for all activities within the biostatistics division.

The ideal candidate will have a bachelor’s degree in computer science, mathematics, statistics, or biostatistics and two years experience in the pharmaceutical industry and with SAS. He/she must be proficient in SAS, have detailed knowledge of CDISC and SDTM standards, and familiarity with all phases of clinical trials and regulatory submissions.

Click here to read more about the Clinical Programmer position at Inovio Pharmaceuticals.

Clinical Trial Associate

This position will set-up and maintain the trial master file, including project documentation files, investigator files, study books, and project databases on more complex projects. He/she will work with the project manager to collect relevant study information on timelines, progress, and resources. The person will coordinate and support clinical team, consultant, and vendor meetings.

The ideal candidate will have a bachelor’s degree. A master’s degree, along with expertise in biology, immunology, bioengineering, cell or molecular biology is preferred. Experience with vaccines is highly preferred. He/she should have up to one year monitoring and/or clinical trial management experience.

Click here to read more about the Clinical Trial Associate position at Inovio Pharmaceuticals.

Medical Editor

This position collaborates with project teams on the development of clinical documents in accordance with all applicable regulations, good clinical practices, and standard operating procedures. He/she will facilitate and manage efficient review and finalization processes for documents produced internally and/or externally by consultants, contractors, and vendors. The person will also collaborate with many different divisions within the company.

The ideal candidate will have a bachelor’s degree in life science with relevant writing experience or in English/communications with relevant science expertise. He/she should have a minimum of four years experience as a medical/scientific writer in the sponsor or CRO setting. Experience with regulatory submissions and knowledge of eCTD formatting is a plus.

Click here to read more about the Medical Editor position at Inovio Pharmaceuticals.