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ICON plc
ICON plc
Asistență medicalăConsultanțăLogistică
ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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Locurile de muncă ale companiei

Senior Clinical Research Associate – South Africa (Remote)

Senior Clinical Research Associate overseeing site monitoring and trial execution for ICON’s sponsor-dedicated research programs. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.

ZAAfrica de SudRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Support sponsor-dedicated research programs using ICON’s global clinical expertise
  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with a focus on quality and ongoing improvement
  • Evaluate site adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
  • Conduct site visits to review performance, address issues, and help deliver trials successfully
  • Partner with cross-functional teams to support timely, accurate data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop relationships with site personnel and stakeholders to support efficient trial operations

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory requirements
  • Demonstrated ability to coordinate multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in a complex environment
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the role is located

Beneficii

  • Base salary with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career development opportunities

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