9 дней назад
Clinical Project Specialist (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Project Specialist (Clinical Research): Supporting clinical trial execution through administrative project management, document coordination, study tracking, and meeting support with an accent on regulatory compliance, study documentation, and cross-functional coordination. Focus on maintaining clinical trial records, monitoring study-specific metrics, coordinating deliverables, and escalating issues across study teams.
Location: Hybrid in Zagreb, Croatia, with 2 or 3 days per week in the Zagreb office
Company
provides consulting and operational solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, medical device, and pharmaceutical organizations.
What you will do
- Provide administrative project management support for clinical trial execution.
- Prepare, format, review, reconcile, collect, distribute, and track study documents in line with organizational processes.
- Support day-to-day study operations and maintain compliance with SOPs, ICH/GCP guidelines, and regulatory requirements.
- Develop and distribute site binders and track study-specific information, site activity, metrics, supplies, and services.
- Coordinate meetings, prepare and distribute meeting minutes, and support study material development.
- Identify and escalate issues, collaborate with study team members and study managers, and contribute to process improvement and quality initiatives.
Requirements
- 2+ years of experience in a pharmaceutical or clinical research environment preferred.
- At least 1 year of Clinical Project Specialist experience preferred.
- Bachelor’s degree preferred; comparable training and experience may be considered.
- Excellent verbal and written communication, interpersonal, presentation, and information summarization skills.
- Strong Microsoft Office skills, including Outlook, Word, Excel, and PowerPoint, plus experience with email and calendar applications.
- Ability to prioritize tasks, plan proactively, work with minimal supervision, and build positive relationships with colleagues and management.
Nice to have
- Experience with electronic data capture systems, CTMS, IVRS, and eTMF.
Culture & Benefits
- Hybrid working model that combines remote work with in-person collaboration.
- Inclusive workplace focused on diversity, equity, and inclusion.
- Environment that encourages innovation, collaboration, entrepreneurship, and authentic self-expression.
- Applications are personally reviewed by the recruitment team, with an outcome communicated to every applicant.
Hiring process
- Applications are reviewed personally by a member of the recruitment team rather than screened by AI tools.
- Applicants receive an outcome on their application, regardless of the final decision.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →