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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

Remote Clinical Operations Specialist, Pennsylvania — ICON plc

Lead regulatory submissions and site activation for ICON Strategic Solutions. Support clinical trial start-up and coordinate stakeholder approvals.

USStatele Unite ale AmericiiPAPennsylvaniaRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăOperațiuni clinice
Google Cloud Platform

Descriere

  • Oversee clinical trial start-up while ensuring regulatory compliance.
  • Support site start-up and activation.
  • Prepare and submit clinical trial applications, ethics committee submissions, and communications with regulatory agencies.
  • Work with internal and external stakeholders to secure approvals and authorizations for study launch.
  • Maintain records of regulatory submissions, approvals, and related correspondence.
  • Advise study teams on regulatory obligations and effective start-up practices.
  • Help improve processes to make study start-up more efficient.

Cerințe

  • Bachelor’s degree in life sciences or a related discipline.
  • At least two years of clinical research or regulatory affairs experience, including study start-up work.
  • Knowledge of clinical trial regulations and guidance, including ICH-GCP and local requirements.
  • Strong organization and project management skills, with the ability to prioritize competing tasks.
  • Clear communication and interpersonal skills for effective cross-functional collaboration.
  • Able to travel when needed, approximately 5%.
  • Legally authorized to work in the country where the position is based.

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 pathways for learning and development.

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