Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources.
We are inspired b... read morey the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality.
Job Summary: The CDP Country Manager will lead all country-level operations, including technical implementation, administration, and oversight. The Country Manager will be responsible for accompl
Job Summary: The Cooperative Development Specialist will lead all project technical operations, including providing technical assistance to partner cooperatives in areas of cooperative business m
We are seeking an Animal Genetics Key Accounts Manager to drive business development and serve as the primary point of contact for strategic partnerships in Nigeria’s livestock and dairy sect
Job Id: R1457506
Job Overview
To work as an integral member of the site management team, which may include but are not limited to site recruitment, ongoing site support, training/support for
Job Overview
Acts as a Lead Medical Writer on projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agre
Job Overview
Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements
Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File
Our Senior Site Activation Specialists perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard o
The Site Monitor Educator is responsible for overseeing and coordinating the activities of site monitors to ensure the successful execution of clinical trials. This role involves ensuring complianc
Job Overview
Supports and manages relationships with pharmacies in global clinical trials up to Phase III with a special focus on clinical trials conducted in the region
Contact for IMP-relate
Our Senior Site Activation Specialists perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard o
Job Overview
Supports and manages relationships with pharmacies in global clinical trials up to Phase III with a special focus on clinical trials conducted in the region
Contact for IMP-relate
Job ID: R1435929
Job Description
As a Site Network Manager, you will be responsible for developing and owning the Partner Site relationships and strategy to deliver growth, differentiation an
Job Description Summary
As a Site Network Manager, you will be responsible for developing and owning the Partner Site relationships and strategy to deliver growth, differentiation and superior p
Job Overview
Drive proactive early engagement and customer management approach creating a pipeline of trial activity in Africa with a key focus on global public health engagements.
Drive marke
Job Overview
Deliver on a variety of activities across clinical operations management to support appropriate business capabilities, analytics and planning ensuring the strategy and operations ar
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File
