Clinical Research Associate II/III (Clinical Research)

Location: Belgrade, Serbia (Hybrid)

Company

hirify.global is a mid-sized global Contract Research Organisation delivering patient-focused clinical development across more than 40 countries.

What you will do

• Perform routine pre-study, initiation, interim monitoring, and closeout site visits independently.
• Manage assigned sites through regular communication with site personnel, supporting compliance, enrolment, and study requirements.
• Conduct CRF reviews and generate and resolve queries according to data review guidelines and applicable data management systems.
• Identify and escalate risks, determine retraining needs, and prepare and follow CAPA plans through timely resolution.
• Prepare documents for ethics committee submissions and notifications, including study-related translations where applicable.
• Negotiate study budgets, support site contract execution, and administer site payments.

Requirements

• University degree, preferably in medical or life sciences, nursing, or another relevant healthcare discipline.
• At least 1–2 years of independent clinical trial monitoring experience.
• Strong knowledge of ICH GCP Guidelines and regulatory requirements, with an interest in clinical research.
• Fluent Serbian or another local language and fluent English, both written and verbal.
• Computer proficiency, strong communication and negotiation skills, and the ability to work independently in a matrix environment.
• Current, valid driver’s license.

Nice to have

• Oncology clinical trial experience.

Culture & Benefits

• Flexible work hours and work-from-home options within the hybrid arrangement.
• Performance and referral bonuses.
• Company car and additional health insurance.
• Employee engagement and well-being initiatives.
• Training and development program.

Hiring process

• Submit a CV for consideration.
• Only shortlisted candidates who meet the requirements will be contacted for the next selection stage.