Safety Physician (m/f)

Région
Wavre
Publication
lundi 8 mai 2017
Date limite
jeudi 8 juin 2017
Réf
740F2XPE-BE
Contact
Carine Steurs
Fonction
Autre
Niveau d'expérience
2 à 5 ans d'expérience
Type de contrat
Fixe
Temps de travail
Temps plein
eXPErt services for eXPErt professionals.
That's XPE. For one of our clients we are looking for: Safety Physician (m/f) Organisation description: Job description:

Your mission will be to actively manage and evaluate risks associated with assigned vaccine projects, and make recommendations for the management and communication of risks in accordance with global legal and regulatory frameworks. This will involve working in partnership with the VCSP Safety Scientist to deliver the following:  Coordinate and perform the medical analysis of adverse event reports and/or signal detection activities for assigned vaccine projects in clinical development and post-licensure  Be the safety contact person for Clinical, Regulatory Affairs, regional and LOC (local operating company) safety managers, manufacturing teams for assigned vaccine projects  Provide medical input to Clinical Teams with respect to safety aspects of the design and preparation of protocols, investigators brochures, investigator letters and reports, for the follow up and processing of clinical study data and lead the safety analyses of the assigned projects.  Ensure creation, maintenance and implementation of (D)CSI (Development, Core Safety Information) for the assigned projects. Your responsibilities will be:  Perform medical review and provide medical advice on safety-related aspects associated with the assigned vaccines.  Signal detection and evaluation of safety for assigned projects.  Manage the evolving safety profile of assigned vaccine projects  Provide appropriate and timely Benefit Risk Assessments for assigned vaccine projects  Design, tracking and follow up of risk management plans for the products assigned and assure their sound implementation.  Lead the Safety Review Team and be VLT (Vaccine Leadership Team) member for assigned vaccine projects  Development and revision of assigned central pharmacovigilance processes and related training.  Answering and follow-up of enquiries from regulatory authorities and other bodies (e.g., Ethics Committees) regarding safety-related aspects.  Implementation of the applicable regulations for the assigned vaccines.  Participate in IDMC meetings or other safety related interactions with outside collaborators of the assigned vaccine projects.

Profile:

Hard Skills

  • Medical Doctor with preferred specialism in Infectious Diseases, Epidemiology or Vaccines
  • Minimum 3 years post-registration clinical experience
  • 2+ years of experience in the Pharmaceutical or Biotech industry working in Clinical Development, Medical Affairs, Pharmacovigilance, Drug Safety or a related field.
  • Knowledge of Pharmacovigilance and signal detection tools, analysis and reporting of medical safety issues for vaccines, taking into account the worldwide regulatory requirements.
  • Knowledge and experience in collection and interpretation of Serious Adverse Events case reports.
  • In depth understanding of the regulatory environment (e.g. International, US and European Legislation).
  • Good understanding of vaccine development process
  • Excellent knowledge of safety regulations and working methods.

Soft Skills

  • Ability to manage crisis, monitor safety issues and work under pressure with a customer and solution oriented approach.
  • Able to prioritise activities effectively and to meet multiple deadlines successfully with attention to detail, setting high performance standards for quality
  • Demonstrate initiative and creativity in performing task and responsibilities. Proactively contributes ideas to improve existing operations
  • Excellent comment of English, written and spoken with strong communication and influencing skills.
  • Integrity and strong feeling for ethics.
  • Computer literate, familiar with using scientific and clinical databases.
  • Good administrative skills, analytical mind.
  • Strong leadership and collaborative working skills
Offer:

Excellent experience in a great pharmaceutical industry Minimum 1 year project



Licenses
XPE Personnel Services NV/SA: Flanders: VG15/BU, Brussels: B-AA5.031, Wallonia: W.RS.002/W.INT.002
XPE Group NV/SA : Flanders: VG1834/B, Brussels: B-AA11.007, Wallonia: W.RS.713