ICH GCP. Meticulous attention to detail in patient data recording. Completion and management of study documentation oversee research activities, ensuring research integrity and compliance. Manage research projects administratively per protocol. Participate in and initiate trial data publications. Oversee regulatory processes, participant Interpret ECGs, CXRs, etc. Address monitoring and data queries. Review and draft SOPs. Prepare source documents
ICH GCP. Meticulous attention to detail in patient data recording. Completion and management of study documentation oversee research activities, ensuring research integrity and compliance. Manage research projects administratively per protocol. Participate in and initiate trial data publications. Oversee regulatory processes, participant Interpret ECGs, CXRs, etc. Address monitoring and data queries. Review and draft SOPs. Prepare source documents
colleagues. Emotional maturity and professional integrity. Excellent spoken and written communication skills eye for detail and desire to probe further into data. Valid driver’s license and reliable transport.
beneficial
beneficial
building relationships with suppliers and customers Integrity / honesty Computer Programs & software (4
building relationships with suppliers and customers Integrity / honesty Computer Programs & software (4
highly beneficial Experience working with electronic data, MS Excel & MS Word Meticulous attention to