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Lead Associate Jobs In Durham Nc - 9 Job Positions Available

1 – 7 of 9 jobs
Worldwide Clinical Trials jobs

Associate Director, Global FP&A Were a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it safe. It

Worldwide Clinical Trials  24 days ago
Worldwide Clinical Trials jobs

Clinical Research Associate Were a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it safe. It is

Worldwide Clinical Trials  23 days ago
Worldwide Clinical Trials jobs

Clinical Trial Associate As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

Worldwide Clinical Trials  17 days ago
IQVIA Holdings jobs

Laboratory Professional Opportunity at IQVIA Laboratories We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories. This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels

IQVIA Holdings  1 day ago
Worldwide Clinical Trials jobs

Clinical Research Associate Were a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it safe. It is

Worldwide Clinical Trials  1 day ago
Worldwide Clinical Trials jobs

Senior Proposal Associate Writing The Senior Proposal Associate Writing role leads proposal writing responsibilities for assigned projects, supports our overall content management, and completes additional proposal writing team tasks as needed. The Senior Proposal Associate Writing role works with Account

Worldwide Clinical Trials  2 days ago
Worldwide Clinical Trials jobs

Associate, Pharmacovigilance Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on small to

Worldwide Clinical Trials  11 hours ago

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