Parexel
Parexel
Parexel yangi dori vositalarini ishlab chiqish jarayonida biofarmatsevtika kompaniyalariga xizmat ko‘rsatuvchi global klinik tadqiqot tashkilotidir. Uning faoliyati I–IV bosqich klinik sinovlari, portfel va tadqiqotlarni boshqarish, tartibga solish strategiyasi, bozorga chiqish hamda hayotiy siklni rejalashtirishni qamrab oladi. 21 000 dan ortiq mutaxassisga ega Parexel klinik, tartibga solish va terapevtik tajribani bemorlar haqidagi tushunchalar hamda innovatsion sinov dizaynlari bilan birlashtiradi. Kompaniya onkologiya, neyrofanlar va kam uchraydigan kasalliklar kabi yo‘nalishlarda tadqiqotlarni qo‘llab-quvvatlaydi hamda klinik ishlab chiqish jarayonini samaraliroq va bemorga yo‘naltirilgan qilishga e’tibor qaratadi.

Senior Clinical Data Manager – FSP (Remote, South Africa)

Lead clinical data management for Parexel’s global pharmaceutical and biotechnology trials. Manage EDC systems, vendors, reconciliations, and database locks across Phase 1–4 studies.

Tavsif

  • Lead major clinical studies or related study programs with limited supervision
  • Represent Data Management in cross-functional clinical trial working groups
  • Oversee clinical data management activities delivered by CROs and external vendors
  • Review protocols and guide data capture strategy, eCRF design, and collection requirements
  • Partner with CRAs, programmers, study managers, statisticians, and other stakeholders on annotated eCRFs and completion guidelines
  • Direct the creation of edit check specifications, data listings, and study-level data management plans
  • Coordinate EDC system design, testing, implementation, and issue resolution
  • Review and advise on monitoring plans, statistical analysis plans, vendor specifications, and related study documents
  • Perform SAE and external data source reconciliations
  • Lead database upgrades, migrations, user acceptance testing, freezes, and locks
  • Maintain study workbooks, data management files, and essential documentation
  • Mentor and train members of the data management team
  • Help develop SOPs, work instructions, and process improvements
  • Participate in team meetings and provide expertise aligned with study and organizational goals

Talablar

  • Bachelor’s degree, preferably in a scientific or healthcare discipline
  • Seven or more years of pharmaceutical or biotechnology data management experience, or equivalent FDA-regulated experience, including study leadership
  • Working knowledge of ICH-GCP, FDA guidance, CDISC, GCDMP, 21 CFR Part 11, MedDRA, WHO Drug Dictionaries, and clinical trial operations
  • Experience using EDC platforms and clinical data management technologies
  • Strong project management, organizational, communication, problem-solving, and multitasking abilities
  • Demonstrated ability to support Phase 1–4 studies and collaborate effectively with vendors and cross-functional teams
  • Familiarity with database upgrades, migrations, user acceptance testing, and advanced data management workflows
  • Strong written and spoken English communication skills
  • Background in pharmaceutical, biotechnology, clinical research, or another FDA-regulated setting
  • Ability to balance competing priorities while protecting data quality and attention to detail
  • Comfort working with EDC platforms, data management tools, clinical databases, and study documentation
  • Oncology or CNS therapeutic experience preferred
  • Experience supporting pivotal Phase III studies preferred
  • Experience training internal and external study teams on EDC platforms and data management procedures preferred

Imtiyozlar

  • Medical aid contribution
  • Gap cover
  • Life assurance
  • Provident fund contribution of 8%
  • 13th cheque
  • Flexible working arrangements
  • Professional development opportunities
  • Exposure to global clinical studies
  • Collaboration with experienced clinical development professionals

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