Clinical Research Associate - Flexible Schedule (Turkey)

IQVIA LLC; Fatih; In loco; TRY 60.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Company car

Mobile phone

Attractive benefits package

Discretionary sign-on bonus

Flexible work schedules

Descrizione del lavoro

IQVIA Turkey is seeking a Clinical Research Associate to join our Sponsor dedicated team as an experienced CRA. You will perform site visits, support recruitment planning, and help ensure regulatory compliance across trials.

Based in Turkey, you will monitor sites, manage data queries, and collaborate with site staff and client representatives while traveling as needed. The role offers growth within a reputable international company with a competitive benefits package.

Competenze

• University degree in scientific discipline or health care
• Requires at least 6 months 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

Mansioni

• 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

Descrizione del lavoro

IQVIA Turkey is seeking a Clinical Research Associate to join our Sponsor dedicated team as an experienced CRA. You will perform site visits, support recruitment planning, and help ensure regulatory compliance across trials.

Based in Turkey, you will monitor sites, manage data queries, and collaborate with site staff and client representatives while traveling as needed. The role offers growth within a reputable international company with a competitive benefits package.