Cochlear

Clinical Operations

• Lead a multi-disciplinary team in the conduct of a cost-effective, ethical and results focused, publishable study that supports the defined business objectives.
• Oversee Site Qualification, Site Initiation, Interim and Close-out Monitoring Visits to ensure Investigator Compliance.
• Liaise with Clinical Research Associate (CRA) to create and implement required study documentation and plans including the study protocol in line with local Institutional Review Board (IRB) or Ethics Committee (EC) requirements, local regulatory guidelines and SOPs to ensure that all studies are conducted in a compliant manner.
• Manage site and subject enrollment, receipt of clinical data and reporting of adverse events to established timelines.
• Act as primary contact between clinic trial sites and sponsor for all study specific needs including routine investigator updates.
• Create and distribute study related metrics to internal and external stakeholders including weekly and monthly updates within team, cross functional teams or senior management, and externally for clinical study sites.
• Anticipate potential obstacles to clinical study success, prepare and communicate contingency plans and implement process improvements.

Clinical Project Manager I

Account Manager

• Develop and demonstrate in-depth knowledge of Cochlear’s product portfolio
• Effectively sell and position Cochlear product features and brand benefits
• Develop and demonstrate business acumen aligned with territory business plan and strategy
• Successfully execute territory business plan assignments with professional and customer partners

Clinical Project Manager I

Associate Clinical Territory Manager