The Clinical Trial Manager (CTM) is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical operations deliverables of clinical trials. This includes but is...

Freelance /Contractual Clinical Research Associate, Dermatology & Rheumatology CRO, Poland The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or...

The Director, Business development will help facilitate the sales and marketing activities for the CRO Business Unit, including managing key accounts, soliciting new business, and being a brand ambassador for Indero...

Indero is seeking a strategic Project Director to oversee a portfolio of dermatology and rheumatology trials, guiding PMs and ensuring delivery of global studies from start‑up to completion. You will partner with...

Indero is seeking a Project Director to oversee a portfolio of clinical studies and manage Project Managers, ensuring delivery to client requirements and regulatory standards. This home-based role in Germany involves...

Indero is a contract research organization specializing in dermatology and rheumatology. The Site Budget and Contract Lead (SBCL) develops investigator budgets and contract proposals, serving as the main contact for...

Indero is seeking a Project Manager with a strong background in clinical project management, especially in dermatology and rheumatology. The role includes overseeing project deliverables, managing budgets, and leading...

Indero seeks an experienced Project Manager to lead clinical research projects. You will coordinate cross-functional teams, manage site activation, and ensure regulatory compliance across GCP/ICH standards. Strong...

Indero is seeking a Project Manager (Europe - Remote) to lead clinical research studies from initiation to closure, ensuring budget and timelines compliance. You will coordinate multi-department tasks, oversee site...

Indero (formerly Innovaderm) is seeking a Contractual Clinical Research Associate to monitor studies at investigative sites or remotely, ensuring trials conform to protocol, SOPs, ICH-GCP, and regulatory requirements....