Associate Director Site Mgt & Oversight Lead Remote

CSL Plasma; Remote; GBP 70,000 - 90,000; Full time

Job summary

A global biotherapeutics leader is seeking an experienced professional for a site management and monitoring oversight role in the United Kingdom. The successful candidate will oversee operational activities across clinical studies, ensuring high-quality execution and regulatory compliance. Responsibilities include managing site performance, engaging with stakeholders, and mitigating risks. Candidates must possess a Bachelor's degree in life sciences and have over 12 years of relevant clinical research experience, particularly in managing large and complex global clinical trials.

Benefits

Comprehensive benefits

Career development opportunities

Supportive workplace culture

Qualifications

• 12+ years of relevant clinical research experience within the pharmaceutical industry.
• Extensive experience in overseeing large global clinical trials.
• Thorough knowledge of ICH guidelines/GCP for clinical development.

Responsibilities

• Provide operational oversight of site management and monitoring activities.
• Support QA audit and inspection planning.
• Build and maintain relationships with site staff and investigators.

Skills

Clinical trial management

Risk mitigation

Stakeholder engagement

Protocol development

Education

Bachelor's degree or equivalent in life sciences

Job description

Position Description and Summary

The Site Management and Monitoring Oversight is 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, this role partners 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 study and site‑level activities, and ensuring that monitoring plans and tools adequately address protocol‑specific risks.

Main Responsibilities

Clinical Oversight & Compliance

• Responsible for operational oversight of the site, site health and monitoring activities
• Support QA audit and inspection planning, and implementation of CAPAs as needed
• Identify and proactively mitigate site‑level risks impacting recruitment, retention, data quality, or compliance, in partnership with CROs

Study Delivery Support

• Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts
• Support sites in understanding study expectations, timelines, and required deliverables
• Be accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets in collaboration with CROs
• Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators/CROs

Site Relationship & Engagement

• Build and maintain strong, trusted relationships with investigators and site staff – Face of CSL
• Serve as the sponsor primary point of contacted for assigned studies
• Understand site capabilities, constraints, and strategic priorities to improve site engagement and long‑term collaboration

Continuous Improvement & Site Experience

• Collect feedback from sites and advocate for process simplification and burden reduction internally
• Identify opportunities to improve study materials, and operational processes
• Represent the “voice of the site” in cross‑functional discussions and initiatives
• Feasibility & Site Selection – provide local site intelligence to feasibility teams
• Support site development

Qualifications and Experience Requirements

• Bachelor’s degree or equivalent in life sciences, nursing, pharmacy, medical laboratory technology
• 12 years + relevant clinical research (or related) experience within the pharmaceutical industry
• Experience in leading and managing a professional team along with site management, monitoring and overseeing large and/or complex global clinical trials
• Extensive experience in drug development process and specifically, each step within the clinical trial process
• Thorough knowledge of ICH guidelines/GCP for all stages in clinical development process
• Experience in overseeing Vendors and CROs
• Robust budget forecasting and management experience
• Successfully demonstrated the ability to mentor and coach others through peer‑to‑peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities
• Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report
• Skilled at independently navigating new or novel indications, study/program approaches, and unique challenges

About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well‑being | CSL.

You Belong at CSL

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.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

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 visit https://www.csl.com/accessibility-statement.