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Monday, April 25, 2011
Product Development Scientist Position
The Product Development Scientist at Accentia Biopharmaceuticals is responsible for providing medical and scientific expertise to clinical product development projects, including the Company’s autologous vaccine for Non-Hodgkin’s Lymphoma and product(s) for treatment of autoimmune disorders.
Also responsible for data analysis and design within clinical workgroups, including development of clinical trial documentation, clinical databases, reviewing and guiding decisions regarding monitoring safety, eligibility, enrollment and data consistency, providing medical expertise and evaluation of questions regarding patient care, and establishing and fostering relationships in the clinical/scientific community and with external experts.
EDUCATION AND PREVIOUS EXPERIENCE
Education: M.D., D.O., PhD or PharmD
Experience: Two to five years of experience in clinical research, medical affairs or clinical development within a postdoctoral research program or in the pharmaceutical or CRO industry preferred. Working understanding of clinical trial design, analysis, and reporting. Working understanding of the drug development process. Ability to recognize safety and efficacy data trends.
Deadline: May 30, 2011
To apply: Please forward your CV to Ivan Sanabria, HR Manager at isanabria@accentia.net or 813-321-7271.
Also responsible for data analysis and design within clinical workgroups, including development of clinical trial documentation, clinical databases, reviewing and guiding decisions regarding monitoring safety, eligibility, enrollment and data consistency, providing medical expertise and evaluation of questions regarding patient care, and establishing and fostering relationships in the clinical/scientific community and with external experts.
EDUCATION AND PREVIOUS EXPERIENCE
Education: M.D., D.O., PhD or PharmD
Experience: Two to five years of experience in clinical research, medical affairs or clinical development within a postdoctoral research program or in the pharmaceutical or CRO industry preferred. Working understanding of clinical trial design, analysis, and reporting. Working understanding of the drug development process. Ability to recognize safety and efficacy data trends.
Deadline: May 30, 2011
To apply: Please forward your CV to Ivan Sanabria, HR Manager at isanabria@accentia.net or 813-321-7271.
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