Regulatory Affairs Specialist

hace 5 días

Alcobendas, Madrid, España Precision Medicine Group A tiempo completo

Job Summary:

Precision Medicine Group is seeking a highly skilled Regulatory Manager to join our team. As a Regulatory Manager, you will be responsible for providing regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures.

Key Responsibilities:

  • Provide regulatory guidance throughout the clinical development life cycle
  • Compile, coordinate and review applications to Regulatory Authorities including, but not limited to, CTA/IND, annual reports, routine amendments, scientific advice/regulatory authority meetings, orphan designations, paediatric planning, and marketing applications
  • Develop and/or review documents intended for submission to the Regulatory Authorities and/or Ethics Committees to assure compliance with regulatory standards
  • Serve as representative of Global Regulatory Affairs at project team meetings with both external and internal customers
  • Work within a project team, and where necessary, lead project for the region or globally
  • Oversee and coordinate Regulatory Affairs Specialists to achieve submission targets for contracted programs
  • Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership updated
  • Assist in development of Regulatory Affairs Specialists and other operational area staff, as required
  • Provide input, as required, into regulatory strategy and timeline development for new study opportunities
  • Assist in establishing company standards to ensure the highest quality of submitted information
  • Participate in maintaining and executing on the corporate quality initiatives across business units within clinical solutions
  • Keep abreast and continually expand knowledge of laws, regulations and guidelines governing drug development and approval
  • Provide ICH GCP guidance, advice and training to internal and external clients
  • Serve as representative of Global Regulatory Affairs at business development meetings

Qualifications:

Minimum Required:

  • Bachelors degree, or equivalent experience, ideally in a scientific or healthcare discipline
  • 5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level
  • Computer literacy (MS Office/ Office 365)
  • Fluent in English

Preferred:

  • Graduate, postgraduate
  • Possesses basic understanding of financial management

Other Required:

Candidates must have regulatory affairs experience working for a Clinical Research Organisation and have experience leading Clinical Submissions

Informed knowledge of all aspects of the drug development process inclusive of regulatory milestones and specialized knowledge of regulatory activities for at least one major region (EU, US) including but not limited to submissions to Regulatory Authorities, including INDs/CTAs and amendments, Scientific Advice Procedures, and post-approval submissions

Ability to understand clinical and pre-clinical study results, to help in its interpretation for regulatory positions and strategy

Knowledgeable of clinical trials methodology, including a working knowledge of protocols and indications being studied

Knowledge and expertise with relevant regulations and guidance supporting pharmaceutical development

Availability for domestic and international travel including overnight stays

Competencies:

  • Strong interpersonal skills and a proven ability to contribute to a team environment involving balancing the demands stemming from multifaceted research activities
  • Demonstrates an acceptable degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates
  • Ability to manage multiple and varied tasks in a fast-moving environment, good record-keeping skills
  • Exhibits high self-motivation, and is able to work and plan independently as well as in a team environment
  • Motivates other members of the project team to meet timelines and project goals
  • Flexible attitude with respect to work assignments, and new learning
  • Resolves project related problems and prioritize workload to meet deadlines with little support from management
  • Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective
  • Collects data of consistently high standard
  • Communicates effectively in the English language both verbally and in written form
  • Conducts formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency

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