for an Industrial Relations Consultant, to be based in Brits . The Consultant is required to reside in Brits
for an Industrial Relations Consultant, to be based in Brits . The Consultant is required to reside in Brits
Description: I am a Specialist Consultant that specialises in placing Finance professionals within the market. My contact: Lorrain Ngwenya on 012 348 4940 Recruitment Consultant: CA(SA),CIMA& General Finance R 500000 -
Description: I am a Specialist Consultant that specialises in placing Finance professionals within the market. My contact: Lorrain Ngwenya on 012 348 4940 Recruitment Consultant: CA(SA),CIMA& General Finance R 500000 -
obtained and recorded and to facilitate the speedy processing of samples in terms of service objectives. Administers of specimens to various laboratories/ sites. Processes sample registration (“logging”) and queries according procedures. Ensures dispatching of specimens for processing in accordance with prescribed standard operating distribute reports and collect submitted samples for processing in accordance with relevant standard operating specimens are received by the designated laboratory, processed and results returned timeously and in compliance
obtained and recorded and to facilitate the speedy processing of samples in terms of service objectives. Administers of specimens to various laboratories/ sites. Processes sample registration (“logging”) and queries according procedures. Ensures dispatching of specimens for processing in accordance with prescribed standard operating distribute reports and collect submitted samples for processing in accordance with relevant standard operating specimens are received by the designated laboratory, processed and results returned timeously and in compliance
documentation. Professional attitude and proactive communication with colleagues. Commitment to professional development accurate, ethical, and efficient clinical trial processes. Conduct clinical trials and provide medical oversight initiate trial data publications. Oversee regulatory processes, participant recruitment, quality assurance, and
documentation. Professional attitude and proactive communication with colleagues. Commitment to professional development accurate, ethical, and efficient clinical trial processes. Conduct clinical trials and provide medical oversight initiate trial data publications. Oversee regulatory processes, participant recruitment, quality assurance, and
and management of study documentation.