Clinical Research Associate

Roles and responsibilities

The role involves the comprehensive oversight and management of clinical trial activities from inception to completion. This includes ensuring strict adherence to regulatory guidelines and study protocols throughout the trial process. The position requires conducting regular site visits to monitor the progress of trials and to ensure the integrity of the data being collected.

Additionally, collaboration with cross-functional teams is crucial to support the overall objectives of the project. This collaborative effort may involve working alongside researchers, data managers, and regulatory specialists to ensure that all aspects of the trial align with established goals. Preparing and submitting all necessary study-related documentation is also a fundamental responsibility of this role, ensuring that all materials are accurate and submitted in a timely manner.

Overall, this position requires a proactive and detail-oriented individual who can thrive in a fast-paced environment. The successful candidate will play a vital role in advancing clinical research initiatives, contributing to the development of new treatments and therapies that can improve patient outcomes.

• A flexible, remote work environment.
• Competitive salary and contract rates.
• Opportunities for professional growth and development.
• Collaborative team culture focused on innovation and success.

Desired candidate profile

Qualifications

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 experience as a Clinical Research Associate (CRA) is required. Conversely, candidates seeking a contract position must have a minimum of 3 years of pertinent industry experience.

Experience in managing phase II-III clinical trials is essential, as it demonstrates familiarity with the complexities and challenges associated with these advanced stages of clinical research. A strong understanding of clinical trial regulations, including Good Clinical Practice (GCP) guidelines, is imperative to ensure that trials are conducted ethically and efficiently.

The ability to work independently is crucial, as the role often requires managing multiple tasks simultaneously while maintaining a high level of attention to detail. Effective time management and organizational skills are necessary to navigate the demands of overseeing clinical trials, ensuring that timelines are met and that the quality of the trial is upheld.