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 Operations Manager – Brazil (Remote)

Manage compliant clinical trial delivery for ICON’s sponsor-dedicated programs. Lead trial execution, performance improvement, and development of clinical operations staff.

Opis

  • Plan and lead clinical trial operations, keeping delivery aligned with protocols and timelines.
  • Work with cross-functional teams to refine trial design and improve efficiency across clinical development.
  • Track trial progress and performance measures, sharing insights to guide decisions and ongoing improvements.
  • Coach and develop junior colleagues while building a collaborative, high-performing team.
  • Develop effective relationships with internal and external stakeholders to support clear communication across clinical operations.
  • Direct trial delivery to meet efficiency, schedule, and regulatory compliance goals.

Zahteve

  • Bachelor’s degree in a relevant scientific or healthcare field.
  • Substantial clinical operations management experience and a strong grasp of regulatory requirements and industry standards.
  • Leadership ability to motivate and manage teams in a changing environment.
  • Experience with project management methods and tools, with a focus on process improvement.
  • Strong communication and interpersonal skills, including the ability to influence stakeholders and achieve outcomes.
  • Able to travel as needed, approximately 30%.
  • Legal authorization to work in the country where the role is based.

Ugodnosti

  • Competitive base pay with performance-related incentives.
  • Health and wellbeing programs, including medical, dental, and vision coverage where available.
  • Retirement and pension plans.
  • Life insurance and disability coverage.
  • Employee assistance programs and wellbeing resources.
  • Structured training and career development opportunities.

Sorodna delovna mesta

IQVIA

Clinical Research Associate, Sponsor Dedicated

IQVIA

Monitor clinical trial sites and support protocol compliance, patient recruitment, and study documentation for IQVIA. Coordinate with site staff and project teams to help trials meet quality standards and milestones.

Odpri
Regeneron

Clinical Study Specialist at Regeneron

Regeneron

Support Regeneron clinical trial teams by coordinating study data, sites, reporting, and close-out activities. Help keep studies on track from site activation through completion.

Odpri