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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

Clinical Associate, Remote in Mexico

Support clinical trial planning, coordination, monitoring, and close-out at ICON, a global clinical research organization. Contribute to the development of treatments through clinical research activities.

MXMexicRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăAsociatGeneral

Descriere

  • Support clinical trial planning, execution, and monitoring in line with protocols, regulations, and industry standards.
  • Coordinate site initiation, patient recruitment, data collection, and monitoring visits, maintaining timely and accurate records.
  • Work with Clinical Operations, Data Management, and Biometrics teams to help deliver clinical trials successfully.
  • Keep study documentation and records complete and compliant with regulations and standard operating procedures.
  • Assist with study close-out, including data cleaning, analysis, and clinical study report preparation.
  • Own clinical coordination deliverables and collaborate with colleagues.

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare field.
  • Experience in clinical research or healthcare, preferably in pharmaceuticals, biotechnology, or a CRO.
  • Strong organizational and time-management skills, including the ability to prioritize and manage competing tasks.
  • Careful attention to detail and sound problem-solving skills, with a focus on data accuracy, integrity, and compliance.
  • Strong communication and interpersonal skills, with the ability to work across teams and build relationships with study teams and clinical sites.
  • Willingness to travel as needed, approximately 60%.
  • Legal authorization to work in the country where the role is based.

Beneficii

  • Base salary and 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.
  • Learning and development through structured training and career pathways.

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