(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA; Turkey; On-site; TRY 150,000 - 300,000; Full time

Job summary

A global contract research organization is seeking a Senior Clinical Research Associate in Turkey. This role involves site selection, monitoring, and ensuring compliance with GCP and ICH guidelines. Ideal candidates should have a degree in a scientific field, at least 2 years of monitoring experience, and excellent command of Turkish and English. The position offers a supportive work environment with career growth opportunities and attractive benefits.

Benefits

Company car

Mobile phone

Attractive benefits package

Career growth resources

Qualifications

• At least 2 years of on-site monitoring experience is required.
• Excellent command of Turkish and English is essential.
• University degree in scientific discipline or health care is mandatory.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate quality and integrity of site practices in accordance with regulatory requirements.

Skills

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 skills

Time management skills

Problem-solving skills

Ability to establish effective working relationships

Flexibility to travel

Driver’s license class B

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