Post Doctoral Research Associate Jobs in Spain

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...

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...

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...

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...

Job Description:About The RoleWe are currently looking for a diligent positive and responsible team player with meticulous attention to detail and high initiative to join our new sports data research team. You will focus on gathering and validating complex data points across sports franchises includ...

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...

Full-timeDescriptionLOCATIONThis position is fully on-site and requires a regular presence in Fort Smith Arkansas. Remote or hybrid work is not available for this position.JOB SUMMARYThe Center for Translational Research within the Research Institute Health and Wellness Center (RIHWC) at ACHE is see...

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...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...