Search by job, company or skills

ICON Strategic Solutions

Clinical Research Associate

Fresher
new job description bg glownew job description bg glownew job description bg svg
  • Posted 18 hours ago
  • Be among the first 10 applicants
Early Applicant

Job Description

Clinical Research Associate


ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmen

t
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycl

e.
What You Will Be Doin

  • g: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standar
  • ds.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial executi
  • on.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporti
  • ng.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial condu
  • ct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operatio

ns.Your Profi

  • le:Advanced degree in a relevant field such as life sciences, nursing, or medici
  • ne.Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requiremen
  • ts.Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skil
  • ls.Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and too
  • ls.Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environme
  • nt.Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's lice

nse

More Info

Job Type:
Industry:
Function:
Employment Type:

Job ID: 135917199