Regulatory Affairs Specialist, Clinical Trial Strategy and Submissions

6 days ago

Singapur, Singapore AbbVie Full time
Job Description

Description

The Regulatory Affairs Specialist is responsible for providing global regulatory expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. The Regulatory Affairs Specialist is responsible for providing operational support as required to the CTS managers / senior managers.

Major Responsibilities

  • Operational support to CTS Leads for submission preparation and processing of initial CTA applications, amendments, end of trial notifications etc.
  • Manage a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments, end of trial notifications etc.
  • Review of and input into documents related to clinical trial submissions managed by other stakeholders such as IB and Protocols.
  • Monthly review and initial assessment of comparators SmPCs which are used in all AbbVie trials.
  • Provide advice on submission strategy, country requirements, etc. as well as operational support for Regulatory submission preparation and processing of amendments.
  • Follow company CTA processes
  • Populate relevant databases, activity trackers and questions database within agreed timelines and compliance/reporting requirements, and provide operational support for Regulatory and/or non-Regulatory systems that are critical for CTA submission and maintenance activities.
  • Provide technical support on document preparation e.g. Excel spreadsheets, Power point presentations.
  • Undertake all necessary training in order to achieve compliance with internal/external processes.
  • Provide operational support for the Clinical Trial Strategy & Submissions team.
  • Support SOP reviews and updates when required.
  • Comply with the company’s policies and procedures to meet statutory, quality and business requirements within the overall strategy and objectives of AbbVie Ltd.

Qualifications

  • Bachelor's degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject is required.
  • Relevant advanced degree in life sciences is preferred
  • 1-2 years Regulatory Affairs or R&D experience preferable.
  • Good Information Technology skills, proven ability to utilise a variety of computer application packages, such as MS Word, Excel, PowerPoint, Adobe Acrobat and global databases.
  • Proactive verbal and written communication style at all levels.
  • Solution driven style.
  • Shows high level of initiative and ability to work independently
  • Has excellent communication/presentation skills, written and verbal; fluency in English.
  • Strong proven personal development and motivational skills.
  • Strong interpersonal, organisational and team working skills.
  • Has critical reasoning skills including the identification and resolution of complex problems and/or elevation of issues to relevant line functions and management.
  • Strong Project Management skills, able to manage multiple activities in line with
  • business priorities and study time goals


Additional Information

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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