Empleos de Precision Medicine Group en España

The CRA I is a seasoned, experienced professional in monitoring and site management. · ...

Precision for Medicine está buscando un Asociado de Factibilidad/Asociado Senior Senior para unirse a su equipo europeo. El trabajo puede ser cubierto completamente remotamente desde España, Polonia, Eslovaquia, Serbia,Rumania o Hungria. · Investigar y analizar información sobre ...

Precision for Medicine is a precision medicine CRO. Precision's uniquely integrated offerings enable the science of precision medicine by combining novel clinical trial designs... · ...

Job Description: · Liaise with project team and senior management of both Precision and sponsors. · Handle and lead all aspects of a clinical research trial or trials. · Total project management for all functional areas including data management, safety, clinical, medical monitor ...

Clinical Research Associate I · Join Precision Medicine Group as a Clinical Research Associate I and be part of our innovative team that supports groundbreaking therapies. · This role involves working independently to manage clinical research studies, ensuring patient safety and ...

Senior Oncology Clinical Trials Project Manager · We are seeking an experienced project manager specializing in oncology clinical trials. · Oversight of multiple projects with varying timelines · Budget management and financial planning · Collaboration with cross-functional teams ...

Our company seeks a Feasibility Associate/Senior Feasibility Associate to join our team. · The ideal candidate will have experience with research and analysis, as well as strong communication and IT skills. · Responsibilities: · <ol style= ...

Job Description · We are seeking an experienced Research Associate to join our team at Precision for Medicine. · Oversight of study site management to ensure patient safety and data quality. · Guidance on audit readiness standards and support for preparation and follow-up actions ...

Job Summary: · Analyzing therapeutic areas to support feasibility assessments for global trials. · Collaborating with various stakeholders to ensure high-quality survey data. · ...

A senior Clinical Research Associate (CRA) II will be responsible for site management and monitoring clinical research studies in Oncology and Cardiology projects. Key responsibilities include: · Ensuring data integrity · Collaborating with cross-functional teams · The ideal cand ...

Key Responsibilities: · Research and compile information on therapeutic areas contained in the clinical protocol · Analyse incidence, prevalence, standard of care, factors determining indication frequency and distribution · Deliver data-driven analysis for pre-&post-award opportu ...

Job Description · We are seeking a highly skilled Regulatory Manager/Senior Regulatory Manager to join our team at Precision Medicine Group. · Bachelors degree or equivalent experience ideally in scientific or healthcare discipline. · A minimum of 7 years' experience working for ...

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. · Private medic ...

Job Title: · Senior Project Manager · Lead clinical projects in accordance with the study budget and scope of work. · Use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects. · Serve as the primary point-of-contact liaison ...

Job Description · A leading clinical research organization in Madrid is hiring a Clinical Research Associate I (CRA I) to manage and monitor clinical trials. · Conducting site visits · Ensuring patient safety · ...

Clinical Research Associate Job Description · The Clinical Research Associate (CRA) II oversees all aspects of study site management to ensure patient safety, quality data generation. · Provides guidance at sites and projects towards audit readiness standards. · Updates trial man ...

Job Description · This position can be performed remotely from Spain. · Candidates should have an advanced degree in life sciences, · strong analytical and communication skills, · ...

+The Clinical Research Associate I is a seasoned professional in monitoring and site management responsible for ensuring patient safety and quality of data. · +Oversees all aspects of study site management to ensure patient safety. · +A university degree in life science/pharmacy/ ...

As Regulatory Manager, you will oversee regulatory aspects of global submissions including preparation and review of documents. This includes ensuring high-quality data management systems to support trials. · Key Responsibilities: · Clinical Trial Planning: Collaborate with cross ...

We invite you to learn more about our growing organization serving clients researching groundbreaking therapies. · Minimum Required: University degree life science/pharmacy/other health related discipline or equivalent experience in a scientific or healthcare discipline or be a l ...