CSL
CSL
CSL — ауыр және сирек кездесетін аурулармен өмір сүретін адамдарға арналған биотерапиялық препараттар мен вакциналар әзірлейтін жаһандық биотехнологиялық және денсаулық сақтау компаниясы. Оның қызметіне иммун тапшылығы, тұқым қуалайтын қан кету бұзылыстары және Альфа-1 антитрипсин тапшылығын емдеуге арналған препараттар ұсынатын CSL Behring; тұмауға қарсы вакциналардың ірі жеткізушілерінің бірі CSL Seqirus; темір тапшылығы мен нефрологияға бағытталған CSL Vifor кіреді. Кең ауқымды зерттеу және әзірлеу желісінің қолдауымен CSL плазманы фракциялау, рекомбинантты ақуыз технологиясы, жасушалық және гендік терапия, сондай-ақ вакциналар бағыттарында жұмыс істейді. Штаб-пәтері Австралияның Мельбурн қаласында орналасқан компания 100-ден астам елдегі пациенттерге қызмет көрсетеді және зерттеу, өндіріс, денсаулық сақтау мен биотехнология салаларында мансап мүмкіндіктерін ұсынады.

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.

Сипаттама

  • 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

Талаптар

  • 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

Артықшылықтар

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

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