(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA LLC

Fatih

Sur place

TRY 360 000 - 480 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Company car
Mobile phone
Benefits package

Résumé du poste

IQVIA Turkey is seeking a sponsor-dedicated Clinical Research Associate to join our team. This role emphasizes on-site monitoring, site selection, initiation, and close-out visits, offering direct exposure to a customer-driven environment within a global CRO.

Qualifications include a university degree in a scientific field, at least 2 years of on-site monitoring, and fluency in Turkish and English. Travel flexibility and a B-class driver’s license are required, with a strong emphasis on

Qualifications

  • University degree in scientific discipline or health care.
  • At least 2 years of on-site monitoring experience.
  • Good knowledge of clinical research regulatory requirements.
  • Very good computer skills including MS Office.
  • Excellent command of Turkish and English language.
  • 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.

Responsabilités

  • 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 (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives

Connaissances

On-site monitoring
Regulatory knowledge
Turkish and English fluency
Time management
Communication skills
Travel flexibility
Driver’s license B

Formation

University degree in scientific discipline or health care

Outils

MS Office

Description du poste

Senior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.

When you join IQVIA Turkey 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.

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.

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 in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Collaborating with experts at study sites and with client representatives
Qualifications
  • University degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements
  • Very good computer skills including MS Office
  • Excellent command of Turkish and English language
  • 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
  • Better Work-Life balance, optimal DOS
  • Excellent working environment in a stabile, international, reputable company
  • Company car, mobile phone and attractive benefits package

For candidates able to start before September 2026, a discretionary sign-on bonus of up to 210,000 TRY may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.

All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

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