Clinical Operations Partner Lead
The role operates across Australia and India, collaborating with teams and stakeholders in both regions to support clinical trial delivery and site management activities.
Responsibilities
Leadership & Team Development
* Lead and develop a team of Site Management professionals, fostering a high-performance, collaborative culture.
* Drive capability building, succession planning, and ongoing development through coaching and mentoring.
Operational Excellence
* Oversee all site management and monitoring activities across Phase I–IV, Oncology, and CGT trials.
* Ensure delivery of country study commitments including patient recruitment, timelines, and data quality.
* Proactively manage performance, identifying risks early and implementing effective solutions.
* Ensure full compliance with ICH‐GCP, regulatory, and local requirements.
Strategic & Business Leadership
* Execute global Site Management strategy at a country level.
* Lead resource planning and budget oversight to ensure optimal trial delivery.
* Provide oversight of CRO partnerships and outsourced studies.
* Drive continuous improvement, contributing to best practices and SOP enhancements.
Stakeholder & Ecosystem Engagement
* Partner cross‐functionally with Medical, Regulatory, PV, and Commercial teams.
* Build and maintain strong relationships with investigators, sites, CROs, and external partners.
* Represent the organisation within the broader clinical research ecosystem.
Quality & Compliance
* Ensure delivery of high‐quality clinical data to support regulatory submissions.
* Maintain audit and inspection readiness across all studies.
* Lead improvements based on audit and inspection outcomes.
Qualifications
* Bachelor's degree in healthcare or life sciences discipline (or equivalent).
* 10+ years' healthcare experience, including 5–7 years in clinical development/operations.
* Proven leadership experience managing clinical operations or site management teams.
* Strong knowledge of global and local clinical trial regulations and GCP standards.
* Demonstrated ability in resource planning, budget management, and stakeholder engagement.
* Experience working within FSP models and/or CRO partnerships is highly advantageous.
Commitment to Diversity and Inclusion
We are committed to creating a culture where people can be their best, in an environment that values inclusion, diversity and flexibility. At Bayer everyone belongs, regardless of race, colour, ancestry, religion, national origin, citizenship, sexual orientation, age, marital status, disability, gender identity, personality, thinking styles or background. We strongly encourage First Nations people to apply.
If you have a disability or special need that requires accommodation, please let us know.
Location
Australia: New South Wales: Pymble
Reference Code
871194
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