Clinical Research Associate

Roles and responsibilities

Clements Partners is a dynamic recruitment firm committed to connecting exceptional talent with leading pharmaceutical organizations. We are excited to announce an opportunity for a Clinical Research Associate (CRA) to join the team of one of our esteemed pharmaceutical clients. This fully remote position is available for candidates across the EMEA region, offering the flexibility to work from any location while contributing to vital clinical studies that shape the future of healthcare.

Key Responsibilities

As a Clinical Research Associate, you will play a pivotal role in overseeing and managing clinical trial activities from inception to completion. Your responsibilities will include ensuring compliance with regulatory guidelines and study protocols, which are critical to the success and integrity of clinical research. You will conduct site visits to monitor trial progress, assess the performance of investigative sites, and maintain data integrity throughout the study lifecycle.

Collaboration is at the heart of this role; you will work closely with cross-functional teams to support project objectives and ensure that all aspects of the clinical trials are aligned with organizational goals. Additionally, you will prepare and submit all necessary study-related documentation, ensuring that the process is smooth and adheres to the required standards.

Desired candidate profile

Qualifications

To qualify for this position, candidates should possess a Bachelor’s degree in Life Sciences or a related field. For those applying for a full-time position, a minimum of 12 months of relevant industry experience as a Clinical Research Associate is required. If you are considering a contract position, you should have at least 3 years of relevant industry experience.

Experience in managing phase II-III trials is essential, as these stages are crucial for the evaluation of new therapies. Candidates must have a strong understanding of clinical trial regulations and Good Clinical Practice (GCP) guidelines.

In addition to technical expertise, successful candidates will demonstrate the ability to work independently and manage multiple tasks effectively. Strong organizational skills and attention to detail are vital, as they contribute to the overall success of clinical trials and the reliability of study results.