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Clinical Trial Assistant en Madrid

Job... IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a...

Descripción del empleo

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

As a Clinical Trial Assistant at IQVIA, you will be responsible for providing administrative support to clinical projects and designated team members fully dedicated to one of our main Clients.

RESPONSIBILITIES:

  • General support in Clinical Monitoring and Regulatory and Start-Up activities.
  • Perform assigned administrative tasks to support team members with clinical trial execution.
  • Accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
  • Collaborate on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness.
  • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Manage site payments.
  • Organize Investigator Meetings if applicable.
  • Collaborate on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:

  • Knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Knowledge of applicable protocol requirements as provided in company training
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
  • Effective written and verbal communication skills.
  • Effective time management and organizational skills
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIREMENTS:

  • Minimum 1-year independent experience as CTA or Project Assistant supporting Clinical Operations teams (CRAs, SSU…)
  • Good command of English and Spanish language
  • Office-based in Madrid

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Información extra

Status
Inactiva
Localización
Madrid
Carnet de conducir
No
Vehículo
No
Carta de motivación
No

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