Clinical Research Associate (Biopharma) job opportunity at AstraZeneca.

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DateMore Than 30 Days Ago bot
AstraZeneca Clinical Research Associate (Biopharma)
Experience: 1-years
Pattern: full-time
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loacation Turkey - Istanbul, Turkey
loacation Turkey - Istan..........Turkey

At AstraZeneca, we unlock the power of what science can do. Empowered to explore, everyday we work towards our ultimate aim – treating, preventing, modifying and even curing complex diseases. With an unwavering belief in following the science, we unleash our curiosity. Investing in key areas, harnessing innovative technologies and taking smart risks. Help to shape the future of healthcare as we take our pipeline from strength to strength. Embrace an environment built on lifelong learning. Never complacent, we seek opportunities to expand our knowledge. The place to build a long-term meaningful career. Here we get to develop and grow – whether that’s working at the leading-edge or on varied stages and molecules. Working on things that have never been done before. In return, when great science comes alive, we have the opportunity to get published. We stand together behind a shared ambition. United by our collective passion for having a positive impact on patients’ lives. Important work that is both meaningful and fulfilling. With the potential to reach over a billion patients across the globe who are living with these complex diseases. Background & Qualifications ​​ University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties), Good level of English, Minimum 1 year of experience in a CRA and/or study coordinator positions Strong communication and negotiation skills, Ability to prioritize and handle multiple tasks, Effective planning and organizational skills with a result-oriented approach, Analytical thinking, critical reasoning ability, Good command of MS Office applications, No restriction to travel, Driving License, No military obligation for male candidates. Job Description Perform monitoring and site management activities for phase trials projects to assess the progress of clinical projects at assigned investigative/physician sites Ensure clinical project is conducted, recorded, and reported in accordance with the protocol, Company SOPs, ICH-GCP, and all applicable local and legal requirements. May assume clinical functional leadership tasks are assigned, actions as Lead CRA for project Train, support and advise Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles. Drive performance at the sites. Proactively identify and ensure timely resolution to study-related issues and escalate them as appropriate. Perform regular Site Quality Risk Assessments and adapt monitoring intensity accordingly during the study. Ensure data query resolution in a timely manner. Work with data management to ensure the robust quality of the collected study data. Collaborate with local MSLs as directed by LSM or line manager. Why AstraZeneca? A high performing team, we work hard to not just meet but go beyond the needs of patients and the wider healthcare industry We leverage our partnerships with external experts across the industry, to create and communicate evidence that changes medical practice. As a partner for many, we effectively communicate complex ideas whilst seeking to understand ever-changing needs and requirements. Our valuable contribution and scientific expertise is responsible for advancing our pipeline and accelerating our pathway to finding a cure. Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you. Where can I find out more? Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Follow AstraZeneca on Instagram https://www.instagram.com/astrazenecaturkiyekariyer/ Date Posted 23-Tem-2025 Closing Date AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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