Job details
Responsible for the end-to-end coordination of cross functional data collection and cleaning activities to ensure clinical study data deliverables are fit for purpose and align with
KPMG is a firm which provides you with an exciting and diverse experience during your articles.
We provide you with excellent support structures to ensure your wellbeing and personal development. T
KPMG is a firm which provides you with an exciting and diverse experience during your articles.
We provide you with excellent support structures to ensure your wellbeing and personal development. T
The Clinical System Set-Up Analyst ensures the technology set-up at a clinical trial’s outset supports the profitability of the trial, ensures quality delivery, and maximizes the ef
The Clinical Database Programmer II provides technical expertise for the conduct of clinical trials and works with minimal supervision to support various programming activities related to clinical
The CSIR has an internship opportunity for Safety Health, Environment (SHE) in the Safety, Health and Environment and Quality (SHEQ) Portfolio. The incumbent will be responsible for supporting the
As Project Leader/ Senior Project Leader you will manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quali
BASIC FUNCTIONS:
Works with Clinical Operations Management staff to ensure the successful management, performance, and career development of Clinical Trial Managers. Provides training and consul
During your 12-month Internship at ERM, you will have unrivalled professional development opportunities, made possible by the breadth and complexity of projects which our clients entrust us to deli
IFC’s Johannesburg Office is seeking an intern as part of our Global Internship Program (GIP). The Global Internship Program (GIP) offers highly motivated individuals an opportunity to be exp
Requirements
QUALIFICATIONS AND ABILITIES / SKILLS:
Matric
Honours in Property Studies
Green Building Certificate ( highly advantageous)
Valid driver's license and own vehicle (
Job Profile:
The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local r
The successful incumbent is a self-starter with a proven track record in maintaining company policy, adopting best practices, and is able to exercise sound judgement in the pursuit of the achieveme
Responsibilities
Supervising of all clinical and administrative aspects of a clinical trial within the research unit to ensure the delivery of the required targets and quality;
Cost control wi
As a QA Auditor, you will conduct complex internal and external audits and inspections to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and
Job Purpose:
To develop and implement strategies for existing & new employer groups, including , stakeholder relations, marketing, communication and sales strategies. To promote and entre
Purpose of Position:
To ensure effective and efficient administrative support to the Facilities Department.
Requirements:
Grade 12
Required Experience:
General administration ex