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*Clinical Research Associate / CRA (m/f/d) - sponsor dedicated, part-time or full time*

Location: Basel, Switzerland
R1247143

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

*Clinical Research Associate / CRA (m/f/d) - sponsor dedicated, part-time or full time*

Apply now
Location: Basel, Switzerland R1247143

Job description

We are currently hiring a CRA (m/f/d) to work in our sponsor dedicated department and to join our team office-based in Basel, St. Prex or home-based in Switzerland in part-time 24-32 h/week or in full-time.  

In our Clinical Functional Service Partnership models, we work in a close partnership with key customers in order 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.

While projects vary, your typical responsibilities might include:

  • 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
  • Conducting remote monitoring

You should have:

  • A Bachelor's or higher level degree in a health care or other scientific discipline or educational equivalent
  • At least one year of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience
  • Excellent communication skills in German and English language and additional good communication skills in French
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements
  • Flexibility to travel

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

Please apply with your English CV, your certificates and reference letters.

#LI-KA1

#CRASDAJD

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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