Clinical Operations Lead: Country Trials

IQVIA Inc in Lisbon, Portugal, seeks a Local Clinical Project Manager to lead country-level study teams and ensure timely delivery of clinical data compliant with ICH-GCP and local regulations. The role involves site selection, qualification, feasibility assessments, regulatory submissions, and maintaining study documentation in CTMS, with travel as...

Acorai is seeking a hands‑on Clinical Operations Specialist to help run and manage clinical investigations validating the SAVE Sensor System in a multi‑centre setting in Portugal. You will ensure studies run to protocol, with complete device recordings and reference measurements documented to regulatory standards.You will design eCRFs, manage data flow,...

Clinical Operations Specialist for a medtech company in Portugal, managing clinical investigations, data review, site monitoring, and documentation for cardiac device validation.

Experienced Global Oncology Clinical Project Lead to manage cross-functional teams in delivering clinical trials on time, within scope, and on budget.

About the Company Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‑to‑end clinical trial solutions across all phases, offering Phase I-IV and...

About the Company Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‐to‐end clinical trial solutions across all phases, offering Phase I-IV and...

AbbVie is seeking a Contract Management Specialist in Portugal to support clinical trials by negotiating and managing contracts, budgets, and related documentation. You will work with Legal, Finance, Clinical Operations, and external sites to ensure timely start-up and compliant study execution.The role requires strong negotiation, communication, and...

MoonLake Immunotherapeutics is seeking a Manager Quality (GCP) to ensure robust GCP compliance across clinical development programs. You will lead audits, manage quality risks, and support inspections readiness while guiding trial teams and vendors to high regulatory standards.The role emphasizes quality systems, CAPA effectiveness, and reporting to senior...

Ensures GCP compliance and quality oversight for clinical development programs. Manages quality risks, supports audits, and ensures inspection readiness.