Responsibilities: •Assisting in the coordination and management of clinical trials •Collecting and organizing data from trial sites •Ensuring compliance with regulatory and ethical standards •Communicating with investigators and site staff •Contributing to the preparation of study documentation Requirements: •Bachelor's degree in a relevant field (e.g., Life Sciences, Nursing, Pharmacy) •Strong attention to detail and organizational skills •Ability to work independently and as part of a team •Knowledge of clinical trial processes and regulations •Excellent communication and interpersonal skills Preferred skills: •Experience in clinical research or healthcare settings •Familiarity with Good Clinical Practice (GCP) guidelines •Proficiency in Microsoft Office applications •Understanding of medical terminology and scientific concepts

Responsibilities: •Assisting in the coordination and management of clinical trials •Collecting and organizing data from trial sites •Ensuring compliance with regulatory and ethical standards •Communicating with investigators and site staff •Contributing to the preparation of study documentation Requirements: •Bachelor's degree in a relevant field (e.g., Life Sciences, Nursing, Pharmacy) •Strong attention to detail and organizational skills •Ability to work independently and as part of a team •Knowledge of clinical trial processes and regulations •Excellent communication and interpersonal skills Preferred skills: •Experience in clinical research or healthcare settings •Familiarity with Good Clinical Practice (GCP) guidelines •Proficiency in Microsoft Office applications •Understanding of medical terminology and scientific concepts