Job Description:
We are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for conducting site visits, developing and implementing recruitment strategies, providing essential training to sites, evaluating and enhancing site practices, and ensuring the seamless execution of clinical trials.
Key responsibilities include engaging with site personnel, identifying areas for improvement, and working collaboratively with a passionate team to support project execution and drive success.
* Conduct site visits to ensure the success of our studies
* Develop and implement innovative plans to recruit study subjects
* Provide essential training and maintain robust communication channels to keep sites aligned and motivated
* Evaluate and enhance site practices to ensure adherence to protocols and regulations
* Monitor every aspect of the study to ensure seamless execution
Requirements:
* A degree in life sciences or healthcare (or equivalent experience)
* 18 months minimum of on-site monitoring experience (ideally oncology)
* Deep knowledge of GCP, ICH, and clinical trial operations
* Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad)
* A proactive mindset, strong communication skills, and a passion for excellence
Benefits:
Join a supportive, innovative team that values your growth and offers flexible work arrangements, travel opportunities, and career development.
Work on diverse, global studies across multiple therapeutic areas, making a tangible impact on project outcomes.
Be part of a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
Why Choose Us:
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.