Więcej informacji
- Numer referencyjny 50/03/2025
- Lokalizacja W Polsce
- Forma wykonywanej pracy praca hybrydowa
- Wymiar czasu pracy część etatu
- Wymagany poziom doświadczenia Brak
- Wymagany poziom doświadczenia student
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Wymagania
Deadline to apply 31st of March
Requirements
Communication Skills - strong written and verbal communication, effective interaction with team members and external partners.
Organizational Skills - ability to manage multiple tasks and priorities, efficient record-keeping and documentation.
Attention to Detail - accuracy in documentation and reporting, ability to identify and correct discrepancies.
Technical and IT Proficiency - proficient in MS Office (Word, Excel, PowerPoint), adaptability to new software and electronic data capture systems.
Time Management Skills - ability to meet deadlines in a fast-paced environment, proactive in prioritizing tasks.
Teamwork and Collaboration - effective work within multidisciplinary teams, supportive of team goals and members.
Eagerness to Learn - enthusiasm for gaining new skills and experiences. -
Poszukiwane kompetencje
Fluent English
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Zakres obowiązków
Responsibilities:
Site Management and Monitoring Poland is responsible for leading and coordinating clinical studies in Poland in various Therapeutic Areas according to AZ values and standards.
We collaborate closely with Study Management Late Phase on quality and timely studies delivery.Main areas of our accountabilities are listed below:
• Studies Administration (management of study documentation including Investigators Study Files and Trial Master Files, EC initial and consecutive submissions, study systems management, contracting and budgeting, Investigator & Sites payments process)
• Studies Monitoring (preparation, execution and follow up on Sites/Remote Visits, interaction and communication with Investigators and Sites, OnSite and remote Study data verification)
• Studies Management (site selection process, management and execution of agreed Study plans, according to timelines based on available tools & metrics)
• Quality Control (inspection readiness & audit/inspection preparation / support, co-monitoring and assessment visits – quality oriented, deployment of available quality KPIs & metrics). -
Oferowane warunki zatrudnienia
All interns will:
- Undergo role-specific training and will be mentored by highly experienced professionals.
- Learn about AstraZeneca and a global pharmaceutical company work environment.
- Undertake real work, proactively collaborating with our experienced staff.
At the end of your internship you will receive a certificate and feedback from the team; many of our interns are successful applicants for permanent roles within our global clinical research centre!
The internships will start in July and last from 3 months.
We work in a hybrid scheme, be prepared to work partially office based.
Don’t miss your opportunity! We are waiting for you!
- Liczba poszukiwanych osób 1
