Clinical Trials Jobs in Belgrade

The PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) and be fluent in English and Slovenian. This is an opportunity for new graduates to start and develop their care...

Research & Insights (50-60%)Lead qualitative research to improve activation and conversion across the trial-to-paid journeyConduct customer interviews using JTBD methodology to understand motivations and adoption patternsDevelop actionable behavioral segments based on customer journeys and desired o...

Provide intelligence on requirements and contribute to the development of the strategy and set up activities including Regulatory Management Plan joint operating procedures POAs and core documents. Support identification of issues.Perform regular screening of regulatory legislative requirements upda...

Provide intelligence on requirements and contribute to the development of the strategy and set up activities including Regulatory Management Plan joint operating procedures POAs and core documents. Support identification of issues.Perform regular screening of regulatory legislative requirements upda...

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process Assures and exerts of activities leading to effective cooperation with clients in the are...

Youll shape and scale the customer research practice for ApprovalMaxs Product Led Growth function. This role offers high autonomy direct influence on product strategy and the chance to establish how customer insights drive decisions in a growing B2B SaaS company.If you thrive on impact over process...

Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site.  Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations procedures and protocols by...

The PV Associate Finnish speaker should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) and be fluent in English and Finnish.This is an opportunity for new graduates to start and devel...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large generic post-marke...

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to determine scheduling...

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Company causality...

The Manager of Global Clinical Budget Development reports to the Associated Director and who works under limited supervision and guidance. This position serves as a subject matter expert in the clinical trial budget development space. Candidate will frequently interact interdepartmentally with R&D P...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large generic post-marke...

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA activities at th...