Creative Clinical Research Associate with extensive project experience from concept to development. Integral team-player with excellent communication skills.
Descripción del trabajo
Key responsibilities include :
1)writing drug trial methodologies (procedures)
2)identifying and briefing appropriate trial investigators (clinicians)
3)setting up and disbanding trial study centres
4)providing clinicians with instructions on how to conduct the trials
5)collecting and authenticating data collection forms (commonly known as case report forms)
6)monitoring progress throughout the duration of the trial
NOTE - Training would be provided (Freshers can apply).
Experiencia laboral (en años)