Clinical Research Associate

i-Pharm Consulting; Ontario; On-site; USD 110,000 - 125,000; Full time

Job summary

Join a leading company as a Clinical Research Associate II or Senior CRA, contributing to innovative biotech trials in oncology and respiratory areas. This role offers opportunities for career progression and involvement in impactful research. Ideal candidates will have 2-3 years of monitoring experience and a relevant degree.

Benefits

401(k)

Vision insurance

Medical insurance

Pension plan

Tuition assistance

Qualifications

• 2-3 years of on-site monitoring experience required.
• Good knowledge of clinical trial regulations (ICH-GCP).

Responsibilities

• Lead site qualification, initiation, monitoring, and close-out visits.
• Ensure compliance with ICH-GCP guidelines and study protocols.
• Foster strong connections with study sites.

Skills

Communication

Organizational Skills

Problem-Solving

Education

Bachelor’s degree in life sciences or healthcare

Job description

This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$110,000.00/yr - $125,000.00/yr

Clinical Research Associate II / Senior CRA

Location: US

Are you an experienced CRA ready to take the next step in your career — are you ready to contribute to ground-breaking research positively impacting patient care?

Join a collaborative team as a Clinical Research Associate II or Senior CRA, supporting a portfolio of biotech clinical trials. This role involves working on complex studies, primarily in oncology, respiratory, and related therapeutic areas, alongside leading investigators and sponsor representatives.

This is a growing team AND a growing company and so offers strong progression opportunities. This includes tailored and development programmes in place to support growth from CRA to CPM or COM.

CRA II

CRA III

Senior CRA

Must have 2–3 years of on-site monitoring experience at a reputable CRO to join a high-impact team working exclusively with a dedicated sponsor in various therapeutic areas.

Key Responsibilities

Lead Site Visits: Take charge of site qualification, initiation, routine monitoring, and close-out visits for exciting biotech clinical trials.

Ensure Compliance: Be the guardian of ICH-GCP guidelines, regulatory requirements, and study protocols, ensuring everything stays on track throughout the study lifecycle.

Build Relationships: Foster strong connections with study sites, ensuring top-notch data integrity and patient safety every step of the way.

Solve Problems: Take initiative in resolving data queries and actively contribute to clinical study documentation and reports.

Support Key Activities: Play a vital role in feasibility assessments, site activation, and driving patient recruitment efforts to keep studies progressing smoothly.

About You

• Bachelor’s degree in life sciences or healthcare.
• At least 2-3 years of independent onsite monitoring experience as a CRA
• Good working knowledge of clinical trial regulations (ICH-GCP).
• Strong communication, organisational, and problem-solving skills.
• Able to work autonomously and travel as required (Regionally).

Why Apply?

• Defined career progression pathways, including opportunities to advance to Project Management or leadership roles.
• Involvement in innovative oncology and biotech trials with global impact.
• Flexible working arrangements and a supportive team culture.
• Access to industry-leading training and professional development.

Looking for a role where your experience is valued, and your career can thrive? Let’s connect.

Apply now or reach out directly to learn more.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research and Science

• Industries

  Research Services and Operations Consulting

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Inferred from the description for this job

401(k)

Vision insurance

Medical insurance

Pension plan

Tuition assistance

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