Study Coordinator

Full-time

VACANCY
Job title: Study Coordinator
Type: Permanent ☒ Fixed Term ☐ Temporary ☐
Main purpose of the job:
To administer, maintain and coordinate the logistical aspects of clinical trials
according to good clinical practice, the study protocol and the standard
operating procedures and to act as a pivotal point of contact for the clinical
trial team and the donors.
Location: 07 Esselen Street, Research Centre, Hillbrow, Johannesburg.
Closing date: 22 September 2021
Submit detailed CV to: Vacancy12@wrhi.ac.za
Advert reference number: NM031 – 2021
In accordance with our Employment Equity goals and plan, preference will be given to suitable applicants
from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments
thereto.

Key performance areas
Assess the project activities and external developments within the field in order to improvement outputs on an
ongoing basis.
Develop/Review work plan and other strategic project documents for the effective implementation of the
project.
Work with colleagues to enhance project goals and outputs.
Identify the needs of the relevant project.
Identify and get resources required.
Coordinate with external agencies such as public health and NGO partners, regulatory bodies, donor
monitoring and auditing agencies and others as necessary
Develop & manage participant/beneficiary recruitment & retention strategies.
Support development of data management monitoring and evaluation plans
Develop and maintain project information systems.
Develop project tools such as SOP’s, informed consents, participant/beneficiary information materials,
technical guidelines, best practice documents and other documents as required.
Coordinate and troubleshoot operational activities such as laboratory activities, pharmacy, IT, procurement
etc.
Conduct training on project processes and activities.
Write project reports for internal/external dissemination.
Present papers and results to stakeholders.
Attend to all staffing requirements and administration.
Supervise and manage the duties of subordinates to ensure optimal staff utilisation and maintenance of sound
labour relations.
Perform and facilitate performance development and assessments through individual coaching and other
support mechanisms.
Identify substandard performance by team members and take necessary corrective action.
Coach and train subordinates and team members to ensure the acquisition of knowledge and skills required
by the organisation.
Promote harmony, teamwork and sharing of information.

Comply with Good Clinical Practice (GCP), Protocol requirements and Standard Operating Procedures
(SOPs).
Verify accuracy of data in source documentation and accuracy of transcription from source data to Case
Report Forms (CRF) as needed.
Ensure errors on source documents e.g., CRF’s are corrected, initialled and dated (as needed).
Support the timely transmission/data faxing of relevant Case Report Forms following QC activity (as needed).
Ensure completion of corrective action of internal and external QC reports and monitoring reviews.
Assist with staff training (and retraining) where error trends are identified.
Prepare files for monitoring visits and requirements.
Meet with Monitors as and when required.
Take ownership and accountability for tasks and demonstrate effective self-management.
Follow through to ensure that quality and productivity standards of own work are consistently and accurately
maintained.
Maintain a positive attitude and respond openly to feedback.
Take ownership for driving own career development by participating in ongoing training and development
activities such as workshops, forums, conferences etc.
Participate and give input in ad hoc projects and initiatives.
Required minimum education and training
Relevant tertiary qualification.
A valid driver’s license, Proficiency in MS office.
Desirable additional education, work experience and personal abilities
Working experience in a medical research environment.
Experience in project management.
Able to work independently and as part of a multi-disciplinary team Thorough with good attention to detail.
Ordered and systematic in approach to tasks, with strict to compliance to protocols.
Exceptional organizational and administrative skills with working knowledge of Microsoft Office.
Able to exercise discretion and independent decision-making.
Able to prioritize own workload, take initiative (pro-active) and work to tight deadlines.
Self-motivated with a high regard for work ethic, values, and integrity.
Good communication skills.
Display a concern for patients and willingness to respond to patients’ needs and requirements.
Required minimum work experience
Minimum 2-3 years clinical trial experience.
Should you be interested in applying for this vacancy, please send an email to Vacancy12@wrhi.ac.za. The
subject heading of the email must read NM031 – 2021 and the job title of position applying for. Please include
the following documentation:
• A cover letter (maximum one page) that clearly states which vacancy you are applying for
• A detailed CV