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Clinical Trials Assistant

Location: Reading, United Kingdom
R1201843

Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors. As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CRAs by CRAs. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level
  • Travel: Yes

Success profile

What makes CRAs aligned to our full-service model successful? Check out the top traits we're looking for and see if you have the right mix.

  • ANALYTICAL
  • ORGANIZED
  • COMMUNICATOR
  • PROBLEM-SOLVER
  • FACILITATOR
  • VERSATILE

Explore this
career path

As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

Quote

Lauren Heffron

IQVIA empowers you to drive your own path within the organization. As no person’s route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and to align your interests with your career goals.

Lauren, Senior Clinical Research Associate 2
Joseph

I really enjoy the diversity of teams and clients the CRA role provides, in addition to the ability to speak with so many different key opinion leaders across the country. Progressing through to a Senior CRA, and now acting as Lead CRA for one of our largest gastroenterology studies, I'm excited at the continued opportunities for success and growth in clinical leadership.

Joseph, Senior Clinical Research Associate 2
Carolina

I work with the most incredible brave minds. We share energy and passion to bring new medicines to the market.

Carolina, Senior Director, R&D Solutions

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Best-in-class Training

    Programs to help you build your therapeutic knowledge

  • Variety

    Dynamic work environments that expose you to new experiences

  • Growth Potential

    Clear pathways to success

  • Therapeutically Aligned

    Protocols aligned to your expertise

Clinical Trials Assistant

Apply now
Location: Reading, Berkshire, United Kingdom R1201843 Posted: 01/07/2022

Job description

Clinical Trials Assistant - UK
Office based role in Reading

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions

• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
• Assist the clinical team with 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 for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Qualifications

• High School Diploma or equivalent 
• 3 years administrative support experience.
• Equivalent combination of education, training and experience.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
• Knowledge of applicable protocol requirements as provided in company training.
#CRAFSAJD

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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