https://bayt.page.link/jcE5ajSPY2RU5SNZ6
أنشئ تنبيهًا وظيفيًا للوظائف المشابهة

الوصف الوظيفي

Work Schedule


Standard (Mon-Fri)

Environmental Conditions


Office

Job Description


Are you ready to embark on a fulfilling career journey with Thermo Fisher Scientific Inc.? We are looking for a motivated and ambitious individual to join our PPD team as a Country Approval Specialist?. This outstanding opportunity allows you to contribute to world-class clinical trials, making a significant impact on global clinical research.


Responsibilities
  • Prepares and performs the submissions to competent authorities including the ethics committees.
  • Collect essential documents for the trial and sites assigned.
  • Reviews, prepares the IP greenlight packages and works with the study team for the site activation readiness.
  • Drive timely clinical trial site activations. Ensure all trial activations are flawless and comply strictly with regulatory standards.
  • Collaborate with cross-functional teams. Work closely with research sites, regulatory, and clinical operations teams to successfully implement trial activation plans.
  • Maintain comprehensive documentation. Keep meticulous records of all trial activation processes and approvals.
  • Identify and address potential issues: Determine any barriers to trial activation and collaborate with teams to resolve them promptly
Requirements
  • Educational background: Bachelor’s degree or equivalent experience in Life Sciences, Pharmacy, or a related field.
  • Experience: Proven experience in clinical trial management, study startup activities or a related research role is preferred.
  • Skills: Outstanding attention to detail, strong organizational skills, and the ability to work collaboratively in a fast-paced, dynamic environment, understanding of clinical trial requirements, regulation and GCP guidelines. .
  • Communication: Excellent verbal and written communication skills to effectively interact with diverse teams, collaborators, and customers.
  • Technical proficiency: Familiarity with clinical trial management systems and regulatory requirements.

Join us on our mission to enable our customers to make the world healthier, cleaner, and safer. Your expertise and dedication will contribute to our continued success and innovation in the scientific community.


لقد تجاوزت الحد الأقصى لعدد التنبيهات الوظيفية المسموح بإضافتها والذي يبلغ 15. يرجى حذف إحدى التنبيهات الوظيفية الحالية لإضافة تنبيه جديد
تم إنشاء تنبيه للوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.
تم إلغاء تفعيل تنبيه الوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.