Резюме від 23 квітня 2024 Файл

Anna

Project Coordinator, Manager

Вік:
35 років
Місто:
Київ

Контактна інформація

Шукач вказав телефон та ел. пошту.

Прізвище, контакти та світлина доступні тільки для зареєстрованих роботодавців. Щоб отримати доступ до особистих даних кандидатів, увійдіть як роботодавець або зареєструйтеся.

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Anna Dyvnych
[відкрити контакти](див. вище в блоці «контактна інформація»)|[відкрити контакти](див. вище в блоці «контактна інформація»)

Professional Summary
A versatile professional with over a decade of experience across varied roles in project management, clinical research, and administrative support. Proven expertise in monitoring study sites, project management, ensuring quality, compliance, and effective use of resources. Demonstrated ability to learn quickly, handle complex tasks, and adapt to new technologies. Proficient in multiple languages and skilled in IT programs and systems. Committed to environment-conscious, sustainable, and inclusive business practices. Eager to apply the diverse skill set in a challenging role to drive organizational growth and success, while making a positive impact on human society.
Skills

• Project Planning
• Networking
• Problem Resolution
• Excellent Communication
• Teamwork and Collaboration
• Fast Learner
• Analytical, Critical and Conceptual Thinking
• Agile Framework (MS Azure)
• Project Management
• Business Ethics
• International Law
• Clinical Research and Development
• Report Writing
• SOP Writing and Revision
• Change Control
• Data Collection and Analysis
• Project Planning
• Networking
• Problem Resolution
• Excellent Communication
• Teamwork and Collaboration
• Written Communication
• Report Writing
• Clinical Documentation
• Data Collection

Work History

Apr 2022 - Dec 2023
SME (Subject Matter Expert) of the Centralised Translation Project
Novo Nordisk
• Supported the team in the continuous delivery of quality products and services.
• Analyzed business problems, identified root causes, and developed robust solutions.
• Improved user productivity and efficiency through product and relevant systems’ training, provided support and hyper-care to the end-users throughout the organization.
• Designed and created video courses on the product for the end-users.
• Monitored user progress to investigate issues and identify improvement opportunities.
• Executed test cases in the TIMS3 system.
• Authored Standard Operating Procedure (SOP), facilitating the organization-wide implementation of the solution.
• Handled change control cases. Change responsible for several cases pertaining to the implementation of the centralised translation process throughout the organization and changes to the validated state of the IT systems.

Aug 2020 - Mar 2022
Clinical Research Associate
Novo Nordisk
• Ensured data quality and patient safety, meeting recruitment targets for clinical trials.
• Conducted monitoring visits to verify study procedures, regulatory documents, and data completion.
• Collaborated with clinical study site team to troubleshoot and provide solutions to study-related issues.
• Reviewed data queries and source documentation and worked with study sites to resolve data discrepancies.
• Supported local safety reporting.
• Managed 7 sites in 4 clinical trials across different therapeutic areas.
• Participated in compliance audits.

Sep 2013 - Jul 2020
Clinical Trial Administrator /
Sr. Clinical Trial Administrator
Novo Nordisk
• Provided clinical trial administration support to Trial Managers and CRAs within the country and adjacent affiliates.
• Facilitated timely and quality delivery of clinical project deliverables through proactive execution of trial-related tasks.
• Oversaw all trial documentation for assigned clinical trials, ensuring compliance with local requirements and Novo Nordisk SOPs.
• Assisted in preparation, submission, and tracking of clinical trial applications and changes to ethics committee and/or health authority.
• Acted as a superuser for relevant IT systems.
• Review and maintenance of trial’s local budget.
• Provided business analytical support to an external partner in the production and implementation of the required IT system in the affiliate.
• Supported the preparation of clinical trial agreements.

Education
Jan 2011
Master of Law: International Public Law and Translation
Institute of International Relations of Taras Shevchenko National University of Kyiv | Ukraine
Jun 2009
Bachelor of Law: International Law
Institute of International Relations of Taras Shevchenko National University of Kyiv | Ukraine

Languages

English: Proficient
Polish: Intermediate

Ukrainian: Native
Russian: Native

Hobbies
Dancing, meditation, sailing.
Additional Information
Driving License: B category.

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