Clinical Research Coordinator Jobs in Spain

Fortreas FSP team is currently seeking a CRA II professionals to join the team in Galicia with specific experience in General Medicine this is a permanent role. Summary of Responsibilities:Clinical site monitoring: conducts routine prestudy initiation and closeout visits ensuring full compliance wit...

Clinical Research AssociateIQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic area...

We are seeking a Clinical Researcher to join the Diabetes and Metabolism Research GroupMain responsibilities and duties:Participate as a Sub-Investigator in clinical trials in obesity.Perform medical visits related to the clinical trials in obesity as per protocol: patients recruitment informed cons...

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Galicia. Summary of Responsibilities:Clinical site monitoring: conducts routine prestudy initiation and closeout visits ensuring full compliance with project plans.Site and patient protection: ensures informed consen...

As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators...

JOB SUMMARYThe Senior Clinical Research Associate II is responsible for the site management site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws Good Clinical Practices and Pfiz...

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies that the investig...

National Travel RequiredPerforms on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies that the investigato...

The Director Clinical Vendor Strategy leads Ergomeds clinical outsourcing strategy and vendor governance across the clinical development portfolio. Partnering with Clinical Operations Vendor Management Therapeutic Strategy Regulatory Quality and Finance teams this role drives vendor selection strate...

Fortreas FSP team is currently seeking two CRA2 professionals to join the team in Barcelona. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within Oncology Gynecology / Hematology / Breast Cancer.Summary of Responsibilities:Responsible for all...

The Paediatric Endocrinology Unit of Vall dHebron University Hospital is a tertiary referral unit covering the whole spectrum of paediatric endocrine disease and works closely with the Growth and Development research group of the Vall dHebron Research Institute (VHIR). The Unit runs an active portfo...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations Good Clinical Practices (GCPs) ICH Guidelines AbbVie Standard Operating Pr...

As a Clinical Research Associate II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigator...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

National Travel RequiredPerforms on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies that the investigato...

The Peripheral Nervous System Unit focuses on two main areas of research. First we develop and validate biomarkers for different neuromuscular diseases including amyotrophic lateral sclerosis (ALS) myasthenia neuropathies and myopathies. Second we work on the implementation of new genetic tests for...

We are seeking a Clinical Researcher to join the Diabetes and Metabolism Research GrouMain responsibilities and duties:Participate as a Sub-Investigator in clinical trials in obesity.Perform medical visits related to the clinical trials in obesity as per protocol: patients recruitment informed conse...

Fortreas FSP team is currently seeking two CRA II professionals to join the team in Madrid. Candidates must have at least 3 - 4 years of experience working on complex clinical trials specifically within oncology early phase and respiratory.Summary of Responsibilities:Responsible for all aspects of s...

Location: Spain (Madrid or Barcelona based) Who we areOptimapharm is a mid-sized global Contract Research Organisation turning science into hope through agile patient-focused clinical development.At Optimapharm youll have the opportunity to work on diverse and meaningful projects that help bring inn...

The SML reports into the Associate Director/Sr. Manager Global Site Management and provides direction and operational expertise for all Clinical Site Management (CSM) integrity quality and timeliness of activities in assigned studies. The position can be assigned to serve as the overall CSM function...