Clinical Research Associate - Oncology - Northeast (Field Based)

Pharmaceutical Research Associates, Inc; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Associate to manage oncology trials and mentor junior staff. This role involves significant travel and requires a strong background in clinical trial monitoring and oncology. The successful candidate will demonstrate leadership and effective communication skills, contributing to the quality oversight of clinical studies.

Benefits

Health insurance

Retirement plans

Flexible benefits

Qualifications

• 2-3 years’ experience in clinical trial monitoring.
• 1-3 years' experience in Oncology trials.
• Knowledgeable of Good Clinical Practice and ICH guidelines.

Responsibilities

• Managing multiple trials within Oncology.
• Mentoring and coaching junior team members.
• Supporting budget development and contract negotiations.

Skills

Communication

Influencing skills

Ability to work independently

Education

B.S. or R.N. in Biological Sciences

Tools

CTMS

EDC

Job description

Overview

As a Clinical Research Associate, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

What will you be doing?

• Managing multiple trials within Oncology
• Focusing on quality of life with regional travel
• Demonstrating leadership through involvement in initiatives and acting as SME for systems and processes
• Mentoring and coaching junior team members
• Training other Study Monitors (SMs) and developing site start-up documents
• Reviewing study documents and representing SMs in meetings
• Taking over LTM report reviews for sites assigned to other SMs
• Supporting budget development and contract negotiations in liaison with colleagues
• Assisting with site visits (ASV)
• Monitoring metrics and KPIs as outlined in the Quality Oversight Plan

Interfaces – Primary/Other:

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team
• Others: Study Physician, Quality and Compliance Managers, Site Staff, Investigators

Qualifications

You Are:

• B.S., R.N., or equivalent in Biological Sciences
• Located near a major airport in the Northeast
• Having 2-3 years’ experience in clinical trial monitoring
• Having 1-3 years' experience in Oncology trials
• Knowledgeable in therapeutic areas and systems like CTMS, EDC, etc.
• Strong communication, influencing skills, and ability to work independently and remotely
• Knowledgeable of Good Clinical Practice, ICH guidelines, and local regulations
• Willing to travel up to 50%
• Legally authorized to work in the US without future sponsorship

What ICON offers: We prioritize a diverse culture that rewards performance and nurtures talent. Benefits include various leave entitlements, health insurance, retirement plans, Employee Assistance Programme, life assurance, and flexible benefits. Visit our careers website for more information: https://careers.iconplc.com/benefits

ICON is committed to inclusion and providing an accessible environment for all candidates. We offer accommodations for applicants with disabilities. If you need assistance, please contact us through the provided link.