Essential Skills: Strong experience with effective oversight of DM vendors in complex drug development programs, preferably oncology experience. Regulatory submissions and audit experience very beneficial. Effective project management DM skills to ensure compliance to both quality and timeline expectations. Ability to Lead and support multiple studies concurrently with minimal oversight by functional manager Proven ability to closely collaborate with cross-functional team members Strong cross-functional understanding on the impact of data management processes to other stakeholders. Has a good understanding of regulatory guidelines and issues (i.e., ICH GCP), and understands the connection to DM deliverables.
https://www1.jobdiva.com/candidates/myjobs/openjob_outside.jsp?a=irjdnw4aqkb0a5bhkjucv8p00hyqhk05031z6ahtakm0pgjg8f34dc29wtyqerjr&from=COMP&id=10785506&SearchString=&StatesString=&jobseq=0&rowsperpage=30&divisions=&divisions2=
No comments:
Post a Comment