Clinical Research Associate II

1 week ago


Columbus, Ohio, United States ICON Strategic Solutions Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate II - Oncology to join our team at ICON Strategic Solutions. As a key member of our clinical trials team, you will be responsible for managing and coordinating clinical trials in the oncology space.

Key Responsibilities
  • Manage and coordinate clinical trials in oncology, ensuring timely and efficient execution
  • Collaborate with cross-functional teams, including investigators, site staff, and internal stakeholders to ensure trial success
  • Conduct site visits and monitor trial progress, identifying and resolving any issues that may impact trial timelines
  • Develop and maintain strong relationships with investigators and site staff to ensure high-quality trial data
  • Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines
  • Participate in trial initiation, maintenance, and close-out activities, including site start-up and study close-out
  • Provide training and support to site staff on trial procedures and protocols
  • Collaborate with internal teams to develop and implement trial strategies and plans
  • Contribute to the development and maintenance of trial-related documents, including study protocols, informed consent forms, and case report forms
Requirements
  • Bachelor's degree in a life science or related field, or equivalent experience
  • Minimum 3 years of experience in clinical research, preferably in oncology
  • Strong knowledge of clinical trials, including GCP, ICH guidelines, and regulatory requirements
  • Excellent communication and interpersonal skills, with ability to work effectively in a team environment
  • Ability to travel up to 50% of the time, with occasional overnight stays
  • Strong analytical and problem-solving skills, with ability to prioritize tasks and manage multiple projects simultaneously
What We Offer

At ICON Strategic Solutions, we offer a competitive salary and benefits package, as well as opportunities for professional growth and development. Our team is dedicated to delivering high-quality clinical trials, and we are committed to providing a supportive and inclusive work environment.

We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced clinical research professional looking for a new challenge, we encourage you to apply for this exciting opportunity.



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