ICON plc
ICON plc
ICON plc je globalna pogodbena raziskovalna organizacija, ki zagotavlja storitve za zdravstveno in farmacevtsko industrijo. Njeno delo vključuje klinične, svetovalne in komercialne storitve, ki podpirajo razvoj zdravil od zgodnjih raziskav do dejavnosti po prihodu na trg. Podjetje ponuja rešitve, kot so decentralizirane klinične raziskave, ocenjevanje srčne varnosti, laboratorijske storitve za zgodnje klinične raziskave, medicinsko slikanje, regulatorne informacije in dokazi iz resničnega sveta. ICON plc ima tudi terapevtsko strokovno znanje na področjih, kot so bolezni srca in ožilja, onkologija, interna medicina, celične in genske terapije ter podobna biološka zdravila, pri čemer združuje analizo podatkov s pristopi, osredotočenimi na paciente, da pomaga napredovati klinične programe.

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.

Opis

  • 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.

Zahteve

  • 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.

Ugodnosti

  • 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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