FAQs
What qualifications are required for the Clinical Trials Assistant position?
A relevant background in clinical research or healthcare, along with a strong commitment to patient care and adherence to research protocols, is preferred.
What is the role of a Clinical Trials Assistant within the R&D team?
The Clinical Trials Assistant supports various specialties by assisting in research activities and ensuring compliance with research protocols and Good Clinical Practice guidelines.
Will I have the opportunity to work in different specialties?
Yes, the post holder will have the opportunity to work across varied specialties to support research in those areas.
What guidelines must be followed in this position?
The post holder must adhere to ICH Good Clinical Practice guidelines, ensuring patient safety and data integrity at all times.
Is patient interaction a part of the Clinical Trials Assistant role?
Yes, the post holder is responsible for providing the highest standards of patient care in line with research protocols.
What kind of training will be provided for this role?
Comprehensive training will be provided to ensure the post holder understands the research protocols and Good Clinical Practice guidelines necessary for the role.
Is experience in clinical trials necessary for this position?
While prior experience in clinical trials is beneficial, it is not mandatory for this trainee position, as training will be provided.
What are the typical working hours for this role?
Working hours may vary but are generally standard office hours, with some flexibility required depending on research activities.
How does this role contribute to patient safety?
The Clinical Trials Assistant plays a critical role in safeguarding patient well-being by ensuring adherence to research protocols and ethical standards.
Are there opportunities for career advancement in this role?
Yes, there are opportunities for career advancement within the R&D team as you gain experience and develop your skills in clinical trials.