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Clinical Research Associate - Single Sponsor

Location: Istanbul, Turkey
R1310124

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 - Single Sponsor

Apply now
Location: Istanbul, Turkey R1310124

Job description

IQVIA Clinical FSP business is unique.  Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients.  We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.

Leadership recognizes the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows.   Our managers understand the sponsors priorities and the individual aspects of each model.  Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.

Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’.  Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties.

Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.

What we Offer:

  • Excellent salary and benefits package
  • Company car
  • Depending on the model, home-based is a possibility
  • Flexible working hours in a home-based role
  • As a CRA, you will receive a company iPad and have use of key developments such as site visit apps, visit reporting apps which allow CRAs to do their day to day job more efficiently!
  • We invest in keeping our teams stable, so workload is consistent
  • We offer genuine career development opportunities for those who want to grow as part of the organization
  • We give the chance to work on cutting edge medicines, right at the forefront of new medicine development

Role Details:

  • Working in partnership with a single-sponsor
  • On site between 6 and 8 days per month, dependent on the sponsor
  • All CRAs and SCRAs are allocated to a dedicated IQVIA Line Manager
  • Permanent employment contract
  • Fantastic work/life balance - flexible working within the core hours of 10 am to 4 pm
  • Sponsor model has reduced travel (approx. 30% or less) due to using ‘Fit for Purpose Monitoring’ which incorporates remote monitoring therefore there is less need for on-site visits

Responsibilities:

  • Site management and monitoring activities across the Turkey
  • Work with sites to adapt, drive and track subject recruitment plan
  • Provide protocol and study training to the assigned sites
  • Create and maintain monitoring visit reports and action plans
  • If appropriate, co-monitor, train and mentor junior members of the team   

Become part of our team at IQVIA Turkey!

We believe in hiring the best talent in the industry.

To become part of our team, you should:

  • Have a degree in Life Sciences
  • Have at least 1 year of independent on-site monitoring experience
  • Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
  • Have in depth GCP knowledge
  • Be flexible with the ability to travel nationwide
  • Hold a full Turkey and clean driving license
  • Possess strong communication, written and presentation skills are a must (must have fluency in English language)
  • With the merger between Quintiles and IMS Health, we now have access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. It’s the next generation of clinical development

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

#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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