Safety Analytics & Reporting (SA&R) Lead
Location:
, Massachusetts
Posted:
December 04, 2017
Reference:
R0015189
% of Time
Job Function and Description
20%
Product management/oversight.

May act as a line manager or mentor to PV Scientists, or as a manager for a product or group of products. Oversees and assumes responsibility for assigned therapeutic products and PV activities through the lifecycle of the product.

Supports an organizational structure that meets the evolving needs of Shire and the GDS department. Fosters a collaborative culture within the product team and to external stakeholders. Ensures therapeutic product governance and communication in support of the SA&R Team Lead, Heads of Medical Safety and SA&R and the Qualified Persons for Pharmacovigilance, including the EEA QPPV.

30%
Aggregate report production.

Oversees or is responsible for the production of periodic and ad-hoc safety reporting for therapeutic team products, where Shire is the Global Safety Database holder. Creates, coordinates, prepares and completes aggregate reports (e.g. PBRER, DSUR, PADER, as well as ad hoc queries or reports) for submission to regulatory agencies around the world. Collaborates with the Global Safety Lead to ensure that all information is available to allow for informed medical review and benefit-risk assessment. Responsible for the quality of the final document and uses Shire's EDMS system to provide quality control.

30%

Safety Review Meetings and signal detection.

Oversee or is responsible for the technical and scientific support for safety surveillance and signal detection activities for assigned Shire products via established signal detection methodology and tools. Evaluate signals promptly in signal detection reports and ad-hoc responses to regulatory authorities.

Responsible for efficiently planning Internal Safety Review Committee and Safety Review Team (SRT) meetings, ensuring that stakeholders provide input from their respective areas of responsibility.

20%
Support for investigational products and registration activities.

Effectively collaborate with stakeholders outside of GDS. Represent GDS department in cross-functional clinical programs and registrational activities and provide GDS support for clinical developmental programs.

Education and Experience Requirements
Include educational requirements or equivalency, required years and type(s) or experience, and
necessary licenses or certificates. Specify which are required and which are preferred. For UK,
please do not use years of experience due to UK Legislation
  • Life Science Degree or Healthcare Professional.
  • Post-graduate qualification in a relevant discipline preferred.
  • Minimum of 8 years previous experience working in a global pharmaceutical Pharmacovigilance Department
  • Supervisory experience preferred
Key Skills, Abilities, and Competencies
Describe critical skill and abilities needed to successfully perform the job, which should be
representative of the knowledge, skills, and abilities required. Reasonable accommodations may be
made to enable individuals with disabilities to perform the essential functions.
  • Experience in the support of post marketing surveillance and reporting to Regulatory Authorities worldwide.
  • Strong understanding of the clinical development and regulatory process.
  • Practical experience in the interpretation of global Pharmacovigilance regulations and implementation within an industry setting.
  • Competence in conducting safety data reviews for investigational and/or post marketed products.
  • High level of expertise and experience in the preparation of aggregate safety reports, including ICH-compliant PBRERs and responses to ad hoc regulatory queries; significant experience in the mentoring, training and assessment of staff involved in the preparation of aggregate safety reports.
  • Experience with MedDRA and drug coding reviews.
  • Ability to contribute to and review standard operating procedures and other process-related documents.
  • Excellent communication, collaboration and networking skills.
  • Strong understanding of the interface between Pharmacovigilance and external departments.
  • Ability to influence others within a matrix environment.
  • Must be able to work in a fast paced environment with demonstrated ability to simultaneously manage multiple competing tasks and demands.
  • Ability to work independently, take initiative and complete tasks to deadlines.
  • Forward-planning and proactive.
Complexity and Problem Solving
Describe the decisions made by the incumbents on a regular basis. Include decisions within the
Incumbent's authority to make as well as those decisions that must be referred to a higher level.

Support global decision-making and direction setting, including devising of future strategy and the management of complex tasks. It is expected that the incumbent will adapt quickly to changing business and healthcare needs, and be autonomous, while working in consultation with the SA&R Team Lead on the implementation of major decisions

Internal and External Contacts
List contacts this job advises, consults, or coordinates with on a regular basis. Describe to whom the
job is accountable. Indicate each Contact category (Internal, Vendor, Customer, or Other) and
provide examples.

Reports directly to SA&R Team Lead . Accountable to the EEA Qualified Person for PV and other senior stakeholders and/or customers. Interacts across multiple functions and geographic locations and supports senior levels of the organization. Particularly important relationships are with Global Clinical Development, Regulatory Affairs, Medical Affairs, and Non-clinical Development. Key external contacts include regulatory agencies, contract research organizations and vendors. Needs to be able to form partnerships with key stakeholders that address the strategic and operational needs of Shire. Represents the department in cross functional initiatives.


A little about us:
At Shire, we help people with rare diseases and specialized conditions live their lives to the fullest.

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