Clinical Research Associate - Oncology - Northeast (Field Based)

Pharmaceutical Research Associates, Inc; Philadelphia, Boston, New York (Philadelphia County, MA, NY); On-site; USD 91,000 - 115,000; Full time

Job summary

A leading clinical research organization seeks a Clinical Research Associate to manage multiple oncology trials. The role involves mentoring junior staff and ensuring quality oversight. Candidates should have a degree in Biological Sciences and experience in clinical trial monitoring. Strong communication and leadership skills are essential, along with a willingness to travel.

Benefits

Health insurance options

Retirement plans

Global Employee Assistance Programme

Life assurance

Childcare vouchers

Gym discounts

Qualifications

• 2-3 years’ experience in monitoring pharmaceutical clinical trials.
• 1-3 years' experience monitoring Oncology trials.
• Knowledge of GCP, ICH guidelines, and local regulations.

Responsibilities

• Managing multiple trials within Oncology.
• Mentoring and coaching junior team members.
• Developing site start-up documents and reviewing study documents.

Skills

Analytical skills

Communication

Leadership

Partnership skills

Education

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

Tools

CTMS

EDC

eTMF

IWRS

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) as Lead SM
• Developing site start-up documents, including SIV agendas
• Reviewing study documents such as Monitoring Guidelines
• Representing Lead Trial Managers (LTMs) and SMs in meetings
• Reviewing reports for sites assigned to other SMs within the same trial
• Supporting country budget development and contract negotiations with CCS colleagues
• Assisting with ASV activities
• Monitoring metrics and KPIs as outlined in the Quality Oversight Plan (QOP)

Interfaces – Primary/Other:

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team
• Other: Study Responsible Physician, Regional Quality and Compliance, Local Drug Safety Officer, Site Manager team, Investigators, and site personnel

Qualifications

You Are:

• B.S., R.N., or equivalent degree, preferably in Biological Sciences
• Located in Ohio near a major airport
• 2-3 years’ experience in monitoring pharmaceutical clinical trials
• 1-3 years' experience monitoring Oncology trials
• Knowledge of multiple therapeutic areas
• Experience with analytical/risk-based monitoring is a plus
• Ability to drive patient recruitment strategies
• Strong partnership skills with investigators and site staff
• Proficient with systems like CTMS, EDC, eTMF, IWRS, safety reporting
• Excellent communication and influencing skills
• Knowledge of GCP, ICH guidelines, and local regulations
• Willingness to travel up to 50%
• Legally authorized to work in the US without future sponsorship

What ICON offers: We prioritize diversity, high performance, and talent development. Benefits include:

• Various leave entitlements
• Health insurance options
• Retirement plans
• Global Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym discounts, and more

Pay Range: $91,336 – $114,170 USD

Actual salary depends on location, experience, education, and skills.

Learn more about working at ICON: https://careers.iconplc.com/benefits

ICON values inclusion and provides accommodations for applicants with disabilities. For assistance, contact us via the provided link.

We encourage you to apply even if you're unsure about meeting all requirements—your skills might be a perfect fit for this or other roles at ICON.