ICON plc
ICON plc
ICON plc ir globāla līgumizpētes organizācija, kas apkalpo veselības aprūpes un farmācijas nozares. Tās darbība ietver klīniskos, konsultāciju un komerciālos pakalpojumus, kas atbalsta zāļu izstrādi no agrīnas izpētes līdz darbībām pēc zāļu nonākšanas tirgū. Uzņēmums piedāvā decentralizētus klīniskos pētījumus, sirds drošuma novērtēšanu, agrīnās klīniskās laboratorijas pakalpojumus, medicīnisko attēlveidošanu, regulatīvo informāciju un reālās pasaules pierādījumu risinājumus. ICON plc ir arī terapeitiskā kompetence tādās jomās kā sirds un asinsvadu slimības, onkoloģija, iekšķīgās slimības, šūnu un gēnu terapijas, kā arī bioloģiski līdzīgas zāles. Apvienojot datu analīzi ar uz pacientu vērstām pieejām, uzņēmums palīdz attīstīt klīniskās programmas.

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.

Apraksts

  • 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.

Prasības

  • 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.

Priekšrocības

  • 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.

Saistītās vakances

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