(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA Tıbbi İstatisti Tic ve Müş. Ltd. Şti. (TR01); Fatih; On-site; TRY 50,000 - 80,000; Full time

Job summary

A leading global provider of clinical research services, IQVIA Turkey is looking for a Senior Clinical Research Associate to drive human health outcomes. You will perform site visits, ensure regulatory compliance, and manage clinical research progress while enjoying a supportive work environment and excellent benefits.

Benefits

Company car

Mobile phone

Attractive benefits package

Resources that promote career growth

Flexible work schedules

Qualifications

• At least 2 years of on-site monitoring experience.
• Driver’s license class B required.

Responsibilities

• Performing site selection, initiation, monitoring, and close-out visits.
• Managing progress by tracking regulatory submissions and data query resolution.
• Collaborating with experts at study sites.

Skills

Organizational skills

Time management

Problem-solving skills

Good knowledge of clinical research regulatory requirements

Excellent command of Turkish

Excellent command of English

Very good computer skills including MS Office

Education

University degree in scientific discipline or health care

Job description

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 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