CRA Trainee.
Barcelona.
Sponsor dedicatedSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success.
We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.
We are agile and driven to deliver
- for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:Why Syneos HealthWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture
- where you can authentically be yourself.
Central to this is our purpose
- Driven to Deliver
- which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
We are continuously building the company we all want to work for and our customers want to work with.
Why?
Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.




Job ResponsibilitiesJOB PURPOSE/SUMMARY:Assists the team and/or Lead CRA in the conduct of all in-house project activities, and providing administrative support to the clinical project team.
Responsibilities typical include preparation, collection, tracking and analysis of data and/or documentation to produce high quality reports.
Performs basic in-house & on-site activities.
CORE

RESPONSIBILITIES:
Handles project correspondenceComposes complex or confidential correspondenceCreates project specific formsTracks study documentation and clinical suppliesTracks site level informationCreates and maintains central filesCreates site files and prepares site initiation packetsOrganizes travel arrangements and meetingsAssists with preparation of meeting minutesOrganizes presentations, material development and scheduling of project specific trainingParticipates in project specific training and project team meetings, as requiredAssists with tracking of site visits and the visit reportsAssists with adverse event report processingHandles receipt and disposition of CRFs from sitesAssists internal & external customers with general informationAssists with in-house Investigator/site feasibility activitiesInitiates required administrative systemsGathers information, searches files & records,



and makes personal contacts to obtain specific information in order to prepare detailed reports for project and company needsOther duties and assignments as requested for the overall performance of the OU and companyOn-site ActivitiesReviews site file for completeness/accuracyPerforms initial review of CRFs for completeness and consistency with source data, including laboratory reports (e.g. all headers complete/consistent, all boxes complete)Handles collection & logging of CRF pagesConducts Investigational Medicinal Product accountability, prepares material for return/destructionAssists with composing visit reports and visit follow-up activitiesQUALIFICATIONS:

Education:
RN, BS/BA, or equivalent.
Previous practical experience with clinical pharmaceutical research studies in a hospital setting, pharmaceutical company, or CRO preferred.
Knowledge of medical and pharmaceutical terminology is desired.
Ability to work on a team and independently when required.
Candidate/incumbent must be proficient in the use of computer and software systems and have an understanding of basic data processing functions.
Excellent decision making, customer service, and interpersonal skills are required.
Good command of written and spoken English language.
Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.
Learn more about Syneos Health. InformationTasks, duties, and responsibilities as listed in this

job description
are not exhaustive.
The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibi

📌 Cra Trainee. Barcelona. Sponsor Dedicated (España)
🏢 Syneos Health
📍 España