Trial Balance Bookkeeper Job Functions: Reconciliations Statutory Returns Creditors & Debtors Cashbook Preparation Of Management Accounts & Reports The post Trial Balance Bookkeeper appeared first on freerecruit
CLINICAL TRIALS UNIT MANAGER
PERMANENT
Trials Unit and the Groote Schuur HIV Clinical Research Building, Groote Schuur Hospital.
The Clinical Trials Unit Manager is responsible for providing smooth clinical trials unit
Responsibilities:
TRIAL BALANCE BOOKKEEPER - (SAP EXPERIENCE) MIDRAND - Immediate start ideal R25 000 per month Financial Payment of all statutory payments, taxes, levies etc TRIAL BALANCE BOOKKEEPER - (SAP EXPERIENCE) MIDRAND - Payment of all statutory payments, taxes, levies etc TRIAL BALANCE BOOKKEEPER - (SAP EXPERIENCE) MIDRAND -
Industry is currently recruiting a Bookkeeper to Trial Balance for offices based in Clayville in Midrand minimum of 12 years of bookkeeping experience to Trial Balance to accurately manage the accounting and responsibilities: Full Bookkeeping function to Trial Balance Full functions Debtors on Sage X3 and Access
your financial experience been taking books to trial balance and dealing extensively with clients? We technology or systems an advantage DUTIES Bookkeeping to trial balance. Accurate daily capturing and processing
your financial experience been taking books to trial balance and dealing extensively with clients? We technology or systems an advantage DUTIES Bookkeeping to trial balance. Accurate daily capturing and processing
/>DUTIES
purpose of the job:
Actively participating in the Signalling Meeting, Drug Safety Committee, and Labelling Committee – and Reviewing or drafting responses to requests on all drug safety matters from Regulatory Authorities for product projects while giving expert medical input to clinical trials. Maintaining good Client relations and ensuring Reviewing or drafting responses to requests on all drug safety matters from Regulatory Authorities. Involvement for Client products. Actively participating in the Drug Safety Committee – signal detection and risk evaluation
Actively participating in the Signalling Meeting, Drug Safety Committee, and Labelling Committee – and Reviewing or drafting responses to requests on all drug safety matters from Regulatory Authorities for product projects while giving expert medical input to clinical trials. Maintaining good Client relations and ensuring Reviewing or drafting responses to requests on all drug safety matters from Regulatory Authorities. Involvement for Client products. Actively participating in the Drug Safety Committee – signal detection and risk evaluation