CSL
CSL
CSL este o companie globală de biotehnologie și servicii medicale care dezvoltă produse bioterapeutice și vaccinuri pentru persoanele care trăiesc cu boli grave și rare. Operațiunile sale includ CSL Behring, care oferă tratamente pentru imunodeficiență, tulburări ereditare de coagulare și deficit de alfa-1 antitripsină; CSL Seqirus, un furnizor important de vaccinuri antigripale; și CSL Vifor, axată pe deficitul de fier și nefrologie. Susținută de o rețea extinsă de cercetare și dezvoltare, CSL activează în domeniul fracționării plasmei, al tehnologiei proteinelor recombinante, al terapiilor celulare și genice și al vaccinurilor. Cu sediul în Melbourne, Australia, compania deservește pacienți din peste 100 de țări și oferă oportunități de carieră în cercetare, producție, servicii medicale și biotehnologie.

Associate Director, Clinical Operations – Site Engagement Lead

Lead strategic clinical site engagement for CSL Behring, a global biotherapeutics company. Shape feasibility, recruitment, retention, trial delivery, and the site experience across clinical programs.

Descriere

  • Set and evolve site-engagement strategies for designated clinical programs and studies
  • Form and direct cross-functional Engagement Teams tailored to specific programs and studies
  • Own engagement planning from protocol development and feasibility through study delivery and close-out
  • Represent the strategic perspective of clinical sites across CSL
  • Convert site input, operational metrics, and external intelligence into guidance on feasibility, site selection, recruitment, retention, study delivery, and site experience
  • Surface risks, obstacles, and improvement opportunities early while constructively testing existing assumptions and processes
  • Bring stakeholders across functions and regions into alignment and incorporate site priorities into study decisions
  • Coordinate a consistent approach to site engagement across CSL teams
  • Drive process simplification, lower site burden, stronger communication, improved quality and efficiency, faster timelines, and cost reduction
  • Document and distribute lessons learned and insights from clinical sites
  • Develop sustained partnerships with institutions, investigators, and collaborating sites
  • Assess investigator and site capabilities, requirements, constraints, and expectations
  • Maintain proactive dialogue with sites about operational patterns, challenges, opportunities, and developments outside the organization
  • Create dependable channels for site feedback and two-way communication with CSL
  • Advocate for site needs while balancing the priorities of investigators, study teams, patients, and the business

Cerințe

  • Advanced degree in life sciences, pharmacy, medicine, or a related health or scientific field
  • At least 10 years of relevant experience in clinical research, clinical operations, medical affairs, site engagement, or a comparable discipline
  • Substantial background in global clinical development
  • Experience spanning the clinical trial lifecycle
  • Extensive experience within a pharmaceutical sponsor or CRO setting
  • Background working internationally across varied regions and cultures
  • Proven ability to lead cross-functional teams and deliver results through influence without direct reporting authority
  • Skill in interpreting complex qualitative and quantitative data and turning findings into actionable recommendations
  • Strong communication, presentation, relationship management, and stakeholder engagement abilities
  • Advanced working knowledge of PowerPoint and Excel
  • Availability and ability to travel regionally and internationally up to approximately 30%
  • International Clinical Trial Management experience, ideally including four or more years
  • Experience operating in fully outsourced or hybrid clinical trial models
  • Prior experience as a Clinical Research Associate
  • Experience in Clinical Development, Clinical Operations, Medical Affairs, MSL, Feasibility, Site Management, or a related function
  • Familiarity with Power BI, Smartsheet, or comparable tools
  • Strategic experience working with investigators, academic institutions, research networks, or other clinical research stakeholders

Beneficii

  • Eligibility for incentive compensation
  • Equity participation
  • Relocation and mobility assistance are not provided
  • Hybrid work arrangement

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