Clinical Research Associate

CliniRx; United States; On-site; USD 80,000 - 125,000; Full time

Job summary

Join CliniRx as a Site Monitor, where you'll play a vital role in ensuring the delivery of site monitoring activities. This position demands a skilled professional with a relevant degree and experience in clinical research, offering the chance to contribute to innovative healthcare solutions in a dynamic environment.

Benefits

Competitive compensation

Opportunities for professional growth

Supportive work environment

Qualifications

• 1-4 years of experience in site monitoring within clinical research.
• Strong understanding of ICH GCP and clinical trial regulations.

Responsibilities

• Ensure adherence to the Site Monitoring Plan and quality timelines.
• Manage sites to minimize Quality Assurance audit observations.
• Assist in identifying new potential sites.

Skills

Understanding of ICH GCP

Excellent verbal communication

Excellent written communication

Multitasking ability

Ability to thrive under demanding timelines

Education

Bachelor’s or Master’s degree in a scientific discipline

Job description

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As a global contract research organization (CRO), we offer a diverse slate of clinical development and resource solutions reflecting both full-service CRO and functional service provider (FSP) models. In supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges we offer our expertise with a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia

We are looking to add a number of CRA's in our US operations over the coming Weeks / Months. Interested? Please read on.

Primary Purpose: We are seeking a skilled Site Monitor to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
• Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
• Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
• Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes.

Work Relations:

• Report to the Manager of Clinical Operations for project, functional, and administrative matters.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative executives.

Value Added:

Your adherence to the quality and timelines of the monitoring plan will be crucial for the efficient delivery of our projects and overall success.

Key Success Factors:

• Timely and high-quality execution of site monitoring activities.
• Prompt report generation and submission to stakeholders.

Qualifications:

• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years of experience in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and thrive under demanding timelines.

Why Join Us?

Be a part of a dynamic team at CliniRx that values innovation, collaboration, and excellence. We offer competitive compensation, opportunities for professional growth, and a supportive work environment.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Information Technology

• Industries

  Research Services

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