Associate Clinical Data Management Director (Biotechnology / Oncology)

Provide oversight for the execution of oncology data management activities at the program level, lead cross-functional teams, and support CDM process improvement initiatives.

Requirements

• Collaborate with cross-functional teams and external partners
• Lead planning and execution of data management activities
• Develop and maintain Data Management timelines
• Track and manage progress towards data deliverables
• Identify and mitigate risks to Data Management deliverables
• Provide expertise in data management and support clinical studies
• Develop and execute procedures for data quality review and data acceptance
• Manage data transfers with CROs and third-party data sources
• Support the transfer, locking, and archiving of study databases
• Lead electronic submission activities for Data Management
• Participate in selecting outsourcing partners for assigned studies
• Provide oversight of vendors providing Data Management services
• Develop and execute study specific training of staff within a project
• Lead or participate in CDM process improvement initiatives
• Promote and be an advocate for CDM internally and externally
• Direct the activities and hold accountable junior data managers and/or data review teams

Benefits

• 401k plan with generous company contributions
• Group medical, dental and vision coverage
• Life and disability insurance
• Flexible spending accounts
• Discretionary annual bonus program
• Sales-based incentive plan
• Opportunity to purchase company stock
• Long-term incentives
• 15 accrued vacation days in the first year
• 17 paid holidays including a company-wide winter shutdown in December
• Up to 10 sick days throughout the calendar year