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CRA Trainee (m/w/d)

Location: Frankfurt am Main, Germany
R1269584

When you join IQVIA as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.

With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

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

Success profile

What makes sponsor-dedicated CRAs at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • COLLABORATIVE
  • DETAIL-ORIENTED
  • COMMUNICATOR
  • INDEPENDENT
  • CURIOUS
  • PROBLEM-SOLVER

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.

  1. CRA 1
  2. CRA 2
  3. Senior
    CRA 1
  4. Senior
    CRA 2
  5. Senior
    CRA 3

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

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Growth Potential

    Clear pathways to success

  • Collaboration

    Teams that work together to achieve common goals

  • Variety

    Dynamic work environments that expose you to new experiences

  • Best-in-class Training

    Programs to help you build knowledge and gain skills

CRA Trainee (m/w/d)

Apply now
Location: Frankfurt/Main, Hesse, Germany R1269584

Job description

Join IQVIA™ as CRA Trainee(m/w/d) in the sponsor dedicated team. In our Clinical Functional Service Partnership models, we work in a close partnership with key customers to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single pharma client and gain direct and in-depth experience of collaborating with this sponsor.

Beside establishing strong relationships with the client and the involved investigators, you will conduct monitoring on complex clinical trials and assure the adherence to good clinical practices, standard operating procedures, and study protocols.

What the traineeship is:

  • A permanent position with onemonth of in-depth training on the Clinical Research Associate job, further months of mentoring and co-monitoring
  • Remote work / home office with high-class remote trainings and guidance combined with work experience on business travel
  • Trainings on clinical research legal regulations and the work methodology as well as on therapeutic area knowledge and the administration and distribution of clinical research supply
  • Gaining a brought work experience at clinical research sites (hospitals and doctor’s offices) by accompanying experienced Clinical Research Associates onsite and remotely

Responsibilities of a Clinical Research Associateinclude:

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Applicants should have:

  • A university degree in a health care or other scientific discipline or educational equivalent
  • Preferably a training in clinical research or work experience as a Trials Assistant, Trial Coordinator, Study Nurse, etc.
  • Alternatively, you should have an equivalent combination of education, training and experience
  • Fluent written and verbal communication skills in German on at least C1 level, including good command of English is mandatory
  • Flexibility to regular business travel and a driving license class B
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
  • Excellent organizational and problem-solving skills
  • Effective time management skills and ability to manage competing priorities
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, apply now and join our team!

Please apply with your English CV and motivation letter as well as your certificates and recommendation letters.

#CRASDAJD

#LI-KA1

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at https://jobs.iqvia.com

Apply now
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