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Experienced Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA

Turkey

On-site

TRY 25,000 - 35,000

Full time

30+ days ago

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Job summary

A leading global provider of clinical research services is seeking a motivated Clinical Research Associate in Turkey. This role offers the chance to gain experience in various therapeutic areas and build a strong career. Responsibilities include site monitoring and ensuring compliance with regulatory requirements. The company supports career growth and offers an attractive benefits package.

Benefits

Company car
Mobile phone
Attractive benefits package

Qualifications

  • Requires at least 1 year of on-site monitoring experience.
  • Experience in Pharma Industry and/or Clinical Trials environment.

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits.
  • Supporting the development of a subject recruitment plan.
  • Evaluating the quality and integrity of site practices.

Skills

Organizational
Time Management
Problem Solving
Turkish
English

Education

University degree in scientific discipline or health care

Tools

MS Office

Job description

Clinical Research Associate

IQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will 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, and build a meaningful, strong career within our organization.

Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  • Collaborating with experts at study sites and with client representatives

Qualifications:

  • University degree in scientific discipline or health care
  • Requires at least 1 year of on-site monitoring experience.
  • Experience in Pharma Industry, and/or Clinical Trials environment
  • Very good computer skills including MS Office
  • Excellent command of Turkish and English language, Turkey based
  • Organizational, time management and problem-solving skills
  • Ability to establish and maintain effective working relationships with co-workers, managers, and clients
  • Flexibility to travel
  • Driver’s license class B

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Excellent working environment in a stabile, international, reputable company
  • Company car, mobile phone and attractive benefits package

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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