Experienced Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA Tıbbi İstatisti Tic ve Müş. Ltd. Şti. (TR01); Fatih; On-site; TRY 25,000 - 35,000; Full time

Job summary

A leading global clinical research company is seeking a Junior Clinical Research Associate in İstanbul. The role involves performing site visits, supporting subject recruitment, and collaborating with study site experts. Candidates should hold a university degree in a scientific discipline and have monitoring experience in the Pharma industry.

Benefits

Company car

Mobile phone

Attractive benefits package

Qualifications

• At least 1 year of on-site monitoring experience required.
• Experience in Pharma Industry or Clinical Trials environment.
• Excellent command of Turkish and English languages.

Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate site practices for compliance with regulations.

Skills

Monitoring experience

Organizational skills

Problem-solving skills

Flexibility to travel

Excellent communication

Education

University degree in scientific discipline or health care

Tools

MS Office

Job description

Clinical Research Associate

IQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will 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, and build a meaningful, strong career within our organization.

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 and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Qualifications:

• University degree in scientific discipline or health care
• Requires at least 1 year of on-site monitoring experience.
• Experience in Pharma Industry, and/or Clinical Trials environment
• Very good computer skills including MS Office
• Excellent command of Turkish and English language, Turkey based
• 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
• 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