Senior Site Management and Monitoring Oversight Lead at CSL

Melbourne Airport, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

28 Jan, 26

Salary

0.0

Posted On

30 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Management, Monitoring Oversight, Clinical Trials, Regulatory Compliance, Risk Management, Performance Tracking, Vendor Collaboration, Audit Preparedness, Team Leadership, Drug Development Process, ICH Guidelines, GCP, Budget Management, Communication, Problem Solving, Therapeutic Area Knowledge

Industry

Pharmaceutical Manufacturing

Description

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Your Opportunity Reporting to the Senior Director Head of Site Management and Monitoring you will be accountable for the strategic and operational oversight of investigational site management and monitoring activities across assigned clinical studies or programs. This role ensures that clinical trials are executed with high quality, regulatory compliance, and operational efficiency, in alignment with global clinical development strategies. Operating within a matrix environment, partnering with internal stakeholders and external service providers to develop and implement study-specific oversight plans, monitor site performance, and proactively identify and mitigate risks. The role is pivotal in maintaining sponsor oversight, validating the effectiveness of site-level activities, and ensuring that monitoring plans and tools adequately address protocol-specific risks. Your Responsibilities will include Site Oversight Execution: Ensure effective sponsor oversight of investigational sites by reviewing monitoring visit reports, site communications, and issue resolution documentation Monitoring Plan Implementation: Support the development and execution of study-specific monitoring plans, ensuring alignment with protocol requirements and risk-based monitoring strategies. Performance Tracking: Monitor site-level performance metrics (e.g., enrollment, data quality, protocol adherence) and escalate concerns to study leadership as needed Vendor Collaboration: Partner with CROs and external service providers to ensure consistent and compliant site management practices across assigned studies Compliance & Inspection Readiness: Contribute to audit and inspection preparedness by validating site documentation, ensuring timely issue resolution, and maintaining oversight logs Act as the primary point of contact both internally and externally (e.g., vendors) as applicable for anything study related Maintain up to date knowledge of the therapeutic area/product candidate(s), clinical practice, competitors, and regulatory considerations Support audits/inspections and resolutions of findings Support in the development of new SOPs, guidelines etc and/ or participate in working groups about new processes Your Skills & Experience Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred As a guide, a minimum of 7 years’ relevant clinical research (or related) experience within the pharmaceutical industry Previous experience in leading and managing a team of professional staff A solid understanding of the drug development process, and specifically, each step within the clinical trial process Experience in site management and monitoring and overseeing large and/or complex global clinical trials Robust budget forecasting and management experience. Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Our Benefits We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL. About CSL CSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL. We want CSL to reflect the world around us At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL Do work that matters at CSL! CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click here. CSL Global Privacy Notice for Job Applicants and Candidates

Responsibilities

The role is accountable for the strategic and operational oversight of investigational site management and monitoring activities across assigned clinical studies or programs. It ensures that clinical trials are executed with high quality, regulatory compliance, and operational efficiency.