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ICON plc
ICON plc
ConsultingHealthcareLogistics
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
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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.

MXMexicoRemoteFull-timeJuniorMiddleEnglish RequiredAssociateGeneral

Description

  • 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.

Requirements

  • 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.

Benefits

  • 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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