Site Identification Lead, Biotech Clinical Trials

Job Overview Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations and present to internal and potentially external stakeholders. Train and support new team members / junior staff. Make recommendations for process improvements. Essential Functions Accountable to ensure...

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team. The role offers opportunities to gain broad therapeutic experience, build a meaningful career, and contribute to high-quality clinical research activities in Spain.Responsibilities include site visits, subject recruitment planning, compliance with GCP/ICH, progress...

As a Site Activation Specialist, you will be a Single Point of Contact for feasibility, site activation, and maintenance for assigned studies. You will review documents, prepare site materials, and update systems.

IQVIA's Global Site Activation team in Spain seeks a Senior Site Activation Specialist to lead complex projects and serve as a single point of contact for investigative sites and project teams. You will ensure SOPs and timelines are followed, perform feasibility, site ID, start-up, and activation activities, and review documents for completeness and...

Worldwide Clinical Trials in Madrid is seeking a Senior Site Contracts Specialist to lead negotiation and finalization of clinical trial site contracts and budgets. You will act as a SME on CTA processes at country and site level, coordinating with sponsors, sites and internal teams. The role requires deep knowledge of ICH-GCP, regulatory requirements, and...

Premier Research is seeking a Clinical Lead II for Rare Diseases / Oncology to join the Clinical Management team in Spain. You will help biotech, medtech, and specialty pharma partners transform ideas into medicines and diagnostics, while growing your skills and balancing life requirements. You will help deliver clinical trial oversight, site management...

Lilly is seeking a Clinical Research Lead to manage site identification, qualification, and overall site management for assigned therapeutic areas. You will drive enrolment readiness, recruitment strategies, and ensure inspection readiness while maintaining strong investigator relationships.The role requires global trial experience, travel 50-75%, and a deep...

Work as a senior data coordinator on clinical and non-clinical trials; producing and validating eCRFs and databases to excellent quality whilst adhering to deliverable timelines. Producing, reviewing and updating eCRF specifications and sections of the Data Handling Manual. Leading clinical coding activities and management of third party data and eCRFs in...

Worldwide Clinical Trials in Madrid is seeking a Senior Site Contracts Specialist to lead negotiation and finalization of clinical trial site contracts and budgets. You will act as a SME on CTA processes at country and site level, coordinating with sponsors, sites and internal teams. The role requires deep knowledge of ICH-GCP, regulatory requirements, and...