Job Description:

SciPro has partnered with a Global Oncology Biopharmaceutical that has experienced tremendous growth over the last 5 years and working. From a scientific perspective they are using a utilizing a proprietary Drug Discovery Platform. This technology allows them to discovery, develop, and deliver new medicines and treatments to patients fighting cancer.With close to 500 heads across the company, they have 1 product already approved and several others in clinical trials. And due to the recent progression in their portfolio, they are looking to bring on a Sr. Manager. This individual will be responsible for leading CDM activities for their clinical trial programs while working cross functionally with other team members and leaders!Qualifications:B.S. M.S. degree in a related field w minimum of 8-10 years of experienceClinical data management experience (PIPIIPIII trials with study set-up, start, and close)Must have worked with Oncology trialsExcellent communication and ability to work cross functionally with team membersKnowledge of CDISC standards (needed for CDM)Familiarity with Clinical trial design analysis and regulatory guidelines (FDACFR, ICH GCP)