Assistant Cra

hace 1 mes


Madrid, España Mygwork A tiempo completo

.This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Work Schedule Other Environmental Conditions Office Job Description Assistant CRA - Barcelona At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.Our Clinical Operations team in Spain is rapidly growing, and we are looking for an Assistant CRA who will be located in Barcelona.The main responsibilities include, but are not limited to:
- Completes study and site management activities as defined in task matrix, and as applicable and directed for study assigned
- Completes and documents study-specific training.Orients and trains on any CRG/study-specific systems
- Provides in-house support during pre-study assessments
- Reviews study data from various sources remotely
- Supports site staff, where applicable
- Supports Essential Document collection, review and updating in systems
- Verifies document collection status and drives action for missing/incomplete/expired documents and open document findings, as directed Education and Experience: Bachelor's Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities.Prior clinical research experience (comparable to 1 year) would be preferable, as well as, knowledge of clinical monitoring through classwork/training that provides the required knowledge skills and abilities.In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered


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