Research Associate

CliniRx has a number of CRA positions available to support a global study in Q1 2025.

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. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence includes key markets such as the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).

Responsibilities include:

1. Deliver on the Site Monitoring Plan by understanding the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
2. Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
4. Continuously enhance technical and soft skills to improve performance and project outcomes.
5. Report to the Manager of Clinical Operations regarding project, functional, and administrative matters.
6. Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Your adherence to quality standards and timelines is crucial for the successful delivery of our projects.

Qualifications:

• Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills.