(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA; Fatih; Vor Ort; TRY 2.235.136 - 3.129.191; Vollzeit

Benefits dieser Stelle

Company car

Mobile phone

Attractive benefits package

Zusammenfassung

A leading global contract research organization is seeking a Senior Clinical Research Associate in Turkey to perform essential tasks such as site selection, monitoring, and adherence to regulatory standards. The ideal candidate should have a degree in a scientific discipline and at least two years of on-site monitoring experience. Proficiency in both Turkish and English is crucial. This position offers a company car, mobile phone, and an attractive benefits package, promoting career growth and a healthy work-life balance.

Qualifikationen

• At least 2 years of on-site monitoring experience.
• Good knowledge of clinical research regulatory requirements.
• Flexibility to travel and driver's license class B.

Aufgaben

• 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.

Kenntnisse

On-site monitoring experience

Knowledge of clinical research regulatory requirements

Computer skills including MS Office

Excellent command of Turkish and English

Organizational and problem-solving skills

Ausbildung

University degree in scientific discipline or health care

Jobbeschreibung

(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye page is loaded## (Senior) Clinical Research Associate - Sponsor dedicated - Türkiyelocations: Istanbul, Turkey: Istanbul, Turkeytime type: Full timeposted on: Posted Todayjob requisition id: R1538810**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.**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 (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 packageIQVIA 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 atIQVIA 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.