Job Description
Responsibilities:
1. Conduct on-site monitoring at hospitals and clinics to oversee the implementation of clinical trials, collect data, and document all clinical study activities.
2. Assist the research team in all stages of clinical trials; efficiently manage and enter study data into electronic and paper-based systems.
3. Train study site staff on study protocols, evaluate local laboratories, and prepare required documentation.
Requirements & Skills:
Strong interest in operational and field activities
Excellent planning, decision-making, and creative thinking abilities
Strong problem-solving skills
Exceptional communication and interpersonal skills
Highly motivated and eager to learn
Team-oriented with a strong sense of responsibility
Proficient in negotiation principles and techniques
Qualifications:
Age: 20–30 years
Gender: No preference
Military Service (for male applicants): Must have completed or be exempted
Education :
Doctor of Pharmacy (Pharm.D.), Medicine (M.D.), or Veterinary Medicine (D.V.M.), or
Bachelor’s degree in Nursing, Biology, Life Sciences, Laboratory Sciences, or Nutrition
