Clin Ops Specialist (CTA) Barcelona.
Sponsor dedicated.
Updated: December 9, 2024
Location: Spain-Europe - ESP-Home-Based (Madrid)
Job ID: 24006607
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
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 accelerate the delivery of therapies because we are passionate to change lives.
Job ResponsibilitiesResponsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions.Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines.Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits.Prepares and maintains site manuals, reference tools and other documents.Maintains, updates, and inputs clinical tracking information into databases.Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client.Manages shared mailbox, processes site requests and routes correspondence appropriately.Coordinates the ordering, packaging, shipping and tracking of site supplies and materials.Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items.May handle receipt, tracking and disposition of Case Report Forms and Queries.Maintains overall awareness in the field of clinical research by completing all necessary and assigned training.QualificationsHigh School diploma or equivalent.Good communication and interpersonal skills.Ability to embrace new technologies.Minimal travel up to 25% may be required.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.
Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.
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