Study Coordinator: Bloemfontein

Full Time
Free State
Posted 4 weeks ago

Clinical Research

Requirements:

Qualification in Healthcare, Medical technologist/ nursing or equivalent

Minimum of 3 Years Study Coordinator experience

Registration with HPCSA/SANC

Driver’s License with own reliable vehicle

Duties & Responsibilities:

Manage the clinical execution of studies

Provides work direction to the study team

Ensure that all participants are assisted and sorted until all visits are done

Handling of all study correspondence – ensure emails and telephone calls are handled in a professional manner etc.

Compiling and update of sources

Provide training to admin personnel on the way forward

Handling all related lab queries

Ensure that all study documentation is completed according to the protocol

Completion and maintaining of the delegation log

Completion of the screening log

Handling of CRA monitor and SIV bookings

Cooperation with CRA during monitoring of visits, addressing queries during visits

Preparation of files and monitoring rooms before a monitor visit takes place

Addressing of action items after each monitor visit.

Cooperate with the data team regarding queries and data entries

Ensure communication with necessary staff members is done if and when new e-CRF guidelines become available.

Job Features

Job CategoryClinical Research
IndustryClinical Research
Minimum QualificationNursing
Experience in YearsMinimum 3 Years
Physical LocationBloemfontein
Benefits OfferedNone

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