CRA Trainee. Madrid. Sponsor dedicated

Requirements

• Education: RN, BS/BA, or equivalent.
• Get to know Syneos Health
• Over 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.
• http://www.syneoshealth.com
• Additional Information
• Tasks, 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 responsibilities.

Benefits

Additional Information

CRA Trainee. Madrid. Sponsor dedicated Syneos 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 Health - We 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 Responsibilities JOB 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 typically 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 correspondence Composes complex or confidential correspondence Creates project specific forms Tracks study documentation and clinical supplies Tracks site level information Creates and maintains central files Creates site files and prepares site initiation packets Organizes travel arrangements and meetings Assists with preparation of meeting minutes Organizes presentations, material development and scheduling of project specific training Participates in project specific training and project team meetings, as required Assists with tracking of site visits and the visit reports Assists with adverse event report processing Handles receipt and disposition of CRFs from sites Assists internal & external customers with general information Assists with in-house Investigator/site feasibility activities Initiates required administrative systems Gathers information, searches files & records, and makes personal contacts to obtain specific information in order to prepare detailed reports for project and company needs Other duties and assignments as requested for the overall performance of the OU and company On-site Activities : Reviews site file for completeness/accuracy Performs 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 pages Conducts Investigational Medicinal Product accountability, prepares material for return/destruction Assists with composing visit reports and visit follow-up activities

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