Experienced Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA; Fatih; On-site; TRY 360,000 - 500,000; Full time

Benefits offered by this job

Company car

Mobile phone

Benefits package

Job summary

IQVIA Turkey is seeking an Experienced Clinical Research Associate to join our Sponsor dedicated team in Istanbul. You will perform site selection, initiation, monitoring and close-out visits, while supporting subject recruitment plans and ensuring regulatory compliance under GCP/ICH guidelines.

You will track submissions, recruitment progress, CRF completion and data queries, collaborating with site staff and client representatives across therapeutic areas.

Qualifications

• University degree in scientific discipline or health care.
• At least 6 months of on-site monitoring experience.
• Turkish and English language proficiency; based in Turkey.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate site practices for regulatory compliance (GCP/ICH).
• Manage regulatory submissions, recruitment, CRF completion and data query resolutions.
• Collaborate with study sites and client representatives.

Skills

On-site monitoring

Regulatory compliance

GCP/ICH knowledge

Turkish language

English language

Travel readiness

MS Office

Team collaboration

Communication skills

Driver’s license

Education

University degree in science

Tools

MS Office

Job description

## Experienced Clinical Research Associate - Sponsor dedicated - TürkiyeApplylocations: Istanbul, Turkey: Istanbul, Turkeytime type: Full timeposted on: Posted Todayjob requisition id: R1537437**Clinical Research Associate****IQVIA Turkey** is looking for talented and motivated team member to join our Sponsor dedicated team as experienced CRA's. 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 6 months 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*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.*This role is suitable for disabled individuals. Priority will be given to candidates registered with İŞKUR.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.comIQVIA 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.