(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA; Turkey; On-site; TRY 50,000 - 70,000; Full time

Job summary

Join a leading global contract research organization as a Senior Clinical Research Associate in Turkey. You'll perform site monitoring and collaborate with experts while enjoying a supportive work environment and career growth opportunities. This role offers a competitive benefits package, including a company car and flexible work schedules.

Benefits

Company car

Mobile phone

Attractive benefits package

Flexible work schedules

Qualifications

• At least 2 years of on-site monitoring experience.
• Good knowledge of clinical research regulatory requirements.

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.

Skills

Organizational

Time Management

Problem Solving

Turkish

English

Education

University degree in scientific discipline or health care

Tools

MS Office

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