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Thermo Fisher Scientific is seeking an Assistant CRA in Madrid to support clinical trials. The role involves managing study activities, training staff, and ensuring compliance with clinical research standards. Candidates should have a Bachelor's in life sciences and prior clinical research experience, along with strong communication and organizational skills.
At Thermo Fisher Scientific youll 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 lifechanging 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 endtoend 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 highquality costefficient 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 studyspecific training. Orients and trains on any CRG / studyspecific systems
Provides inhouse support during prestudy 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 :
Bachelors Degree in a life sciencerelated 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.
Knowledge Skills and Abilities :
Basic medical / therapeutic area knowledge and understanding of medical terminology Ability to attain and maintain a working knowledge of ICH GCP applicable regulations and PPD clinical research services procedural documents
Effective oral and written communication skills. Fluency in English and Spanish language is essential
Excellent interpersonal and customer service skills
Good organizational and time management skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively
Proven flexibility and adaptability
Ability to work in a team or independently as required
Welldeveloped critical thinking skills including but not limited to : critical mindset indepth investigation for appropriate root cause analysis and problem solving.
Proficient computer skills with good knowledge of MS Office ability to learn and use appropriate software.
Ability to extract pertinent information from all study documents electronic study data systems CTMS and dashboards
Why Join Us
We hire the best develop ourselves and each other and recognise the power of being one team. We understand that you will want to grow bothexpertly and personally throughout your career and therefore will benefit from an awardwinning learning and development programme ensuring you reach your potential.
What We Offer :
As well as being rewarded a competitive salary we have an extensive benefits package based around the health and wellbeing of our employees. We have a flexible working culture where PPD clinical research services truly value a worklife balance. Weve grown sustainably year on year but continue to offer a collaborative environment with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.
Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values Integrity Intensity Innovation and Involvement working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.
How to apply : Please submit your CV in English.
Key Skills
Fashion Retail,Engineering,IFRS,Axapta,Computing
Employment Type : Full-Time
Experience : years
Vacancy : 1