Cochlear24 jobs

Clinical Evaluation Manager

Mid levelSeniorFull-timeOfficeSydney NSW, AustraliaBelconnen ACT 2617, AustraliaPosted 1 month agoVerified 1 month ago
Pending fitX of Y criteria met

About the job

The Clinical Evaluation Manager at Cochlear plays a pivotal role in transforming lives by overseeing a global team dedicated to developing clinical evaluation documentation for implantable hearing solutions. This job is all about making a difference, ensuring high-quality and scientifically robust documentation while fostering a culture of growth and collaboration. Join a team that values diverse perspectives and is committed to continuous improvement, all while helping people hear and be heard.

Meet the team

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You'll be responsible for

📊

Leading clinical evidence planning

Lead the planning, assignment and delivery of clinical evidence and scientific dissemination assets across the Clinical Evaluation team.
✅

Ensuring compliance and quality

Ensure delivery of Clinical Evaluation Plans, Clinical Evaluation Reports, Summaries of Safety and Clinical Performance (SSCPs), systematic literature reviews and manuscripts to agreed timelines and quality standards.
🔧

Driving continuous improvement

Drive continuous improvement in templates, workflows and documentation practices.

Key criteria

🎓

Degree in relevant field

Bachelor's degree in life sciences, medicine, or related discipline.

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📄

Experience in scientific writing

Proven experience in scientific documentation and regulatory standards.

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👥

Demonstrated people leadership

Experience coaching and developing geographically dispersed teams.

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A meaningful career starts with a match

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5 criteria for this job
Degree in relevant field
Bachelor's degree in life sciences, medicine, or related discipline.

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Experience in scientific writing
Proven experience in scientific documentation and regulatory standards.

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Demonstrated people leadership
Experience coaching and developing geographically dispersed teams.

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Strong organisational skills
Ability to manage multiple workflows in a regulated environment.

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Familiarity with medical devices
Understanding of implantable medical devices or hearing health.

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