Job summary:
the clinical research associate will be responsible for overseeing the monitoring of patient data and study-related information related to clinical study sites and clinical trial participation. They will ensure that the investigator adheres to research protocols, regulatory requirements, and good clinical practices.
key responsibilities:
* assist the clinical research team in preparing safety reports.
* monitor and report technical complaints, adverse events, and special case scenarios within 24 hours of receipt.
* distribute marketing samples (where applicable).
requirements:
* familiarity with clinical trials and regulatory requirements.
* strong analytical and problem-solving skills.
* excellent communication and interpersonal skills.
why this role is important:
this role plays a critical part in ensuring the integrity and quality of clinical research studies. The successful candidate will have a keen eye for detail, excellent communication skills, and the ability to work well under pressure.
what we offer:
we are committed to providing our employees with opportunities for growth and development. This includes access to ongoing training and education, as well as opportunities for advancement within the company.