(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye at IQVIA

İstanbul, İstanbul, Türkiye

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

University degree in a scientific discipline or healthcare
At least 2 years of on-site monitoring experience
Good knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Very good computer skills, including MS Office
Excellent command of Turkish and English languages
Organizational, time management, and problem-solving skills
Ability to establish and maintain effective working relationships with co-workers, managers, and clients
Flexibility to travel

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
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

Skills

Key technologies and capabilities for this role

GCPICH guidelinesMS OfficeTurkishEnglishOn-site monitoringSite initiationSite close-outCRF completionData query resolution

Questions & Answers

Common questions about this position

What is the salary for this Senior Clinical Research Associate position?

This information is not specified in the job description.

Is this role remote or onsite?

The position is onsite.

What skills and experience are required for this role?

Requirements include at least 2 years of on-site monitoring experience, good knowledge of GCP and ICH guidelines, very good computer skills including MS Office, excellent Turkish and English, and strong organizational, time management, problem-solving skills, plus flexibility to travel.

What kind of training and development opportunities does IQVIA offer?

The role provides access to world-class training and mentoring, allowing development in a variety of therapeutic areas, with the stability and resources of a leading global CRO.

How should I apply for this position at IQVIA?

Interested candidates should explore opportunities at https://jobs.iqvia.com.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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