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.
Senior Clinical Research Associate, Oncology (France, Remote)
Monitor oncology trials for ICON Strategic Solutions, overseeing site performance, protocol compliance, data quality, and regulatory standards. Support reliable trial conduct through site visits, team collaboration, and guidance for site staff and CRAs.
Apraksts
- Manage clinical trial activities in line with study protocols, regulations, and industry standards.
- Lead technically complex monitoring work, promoting quality and ongoing improvement.
- Check that trial sites follow study protocols, regulatory requirements, and Good Clinical Practice standards.
- Visit sites to review performance, resolve issues, and support trial delivery.
- Work with cross-functional teams to coordinate timely, accurate data collection and reporting.
- Train and advise site staff and fellow CRAs.
- Develop and sustain productive relationships with site teams and stakeholders.
Prasības
- Bachelor’s degree in a relevant science or healthcare field.
- Substantial Clinical Research Associate experience and a strong grasp of trial processes and regulatory requirements.
- Ability to oversee several sites and projects at once, supported by strong organization and problem-solving skills.
- Strong knowledge of monitoring, data integrity, and site management, including relevant clinical trial software and tools.
- Excellent communication, relationship-building, and stakeholder management skills, with the ability to influence compliance in a complex setting.
- Able to travel as needed, approximately 60% of the time.
- Legal authorization to work in the country where the role is based.
Priekšrocības
- Base salary and performance-related incentives.
- Health and wellbeing programmes, including medical, dental, and vision coverage where available.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Structured training and career development opportunities.