RESPONSIBILITIES
Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer
Ability to administr
Main responsibilities
Provide leadership and vision to the team
Manage and deliver several large scale, high complexity/non-standard aspect studies across a range of sponsors and Therapeutic a
REF NO: DEDEAT/2024/04/09
REQUIREMENTS:
National Diploma (NQF L6) in Monitoring and Evaluation/ Public Administration or Management/ Strategic Management and or relevant qualification.
E
REF NO. DoE-AC51/04/2024
REQUIREMENTS:
A grade 12 certificate with no experience required.
Effective communication skills (written and verbal skills) and a good command of English language.
Requirements
We are looking for a diligent and committed individual who has:
An LLM or Masters Degree in Economics.
At least 8 years work experience in complex economic and legal analysis o
Key Responsibilities:
Duties include, amongst others:
The investigation, research and analysis of the effects of mergers in terms of the Competition Act.
Report writting
Liaison with merg
How you will make a difference:
Diligent Administration – contribute and ensure that Diligent remains the source of truth for accurate Entity information, Documentation &
Job description
Client Relationship Management:
Act as the primary point of contact for clients, building and maintaining strong relationships.
Proactively conduct regular meetings with cli
Job Summary
We are a diverse and varied team of focused purchasing colleagues covering Vestas' MED. MED Regional Procurement Organization (RPO) is responsible for managing MED (Southern Europe,
THE JOB AT A GLANCE
As a Customer Account Executive, you will be responsible for growing the number of lives within the COID business through effective customer engagement and the position of a val