Clinical research is a vital component of drug development and innovation, allowing new treatments and medications to reach the market.
Job Role
This full-time position involves working on-site and encompasses a variety of responsibilities, including adhering to regulatory requirements, ethical standards and Good Clinical Practice (GCP) guidelines for assigned trials.
You will be responsible for managing and coordinating study participants throughout the trial process, as well as dispensing and administering investigatory products and conducting related data entry tasks.
Effective communication and collaboration are essential skills for this role, as you will work closely with the study team, including ethics, recruitment, coordinators and Investigators.
Additionally, you will have the opportunity to gain experience working in clinical trials and develop your skills in areas such as GCP, regulation, ethics, privacy and other applicable guidelines.
About You
To succeed in this role, you must be a qualified pharmacist with relevant experience, possess excellent communication and organisational skills, and have experience using various computer applications, databases and electronic medical records.
Our organisation is committed to delivering high-quality services and meeting the needs of our clients. We strive to provide a collaborative and supportive environment that fosters growth and development.