Job Title: Associate Director, Signal Management and Innovation (Remote role)
Duration: 5 months contract
REMOTE ROLE
Objective / Purpose:
Ensures signal detection, evaluation and management processes meet highest standards by working cross functionally and leading the development of required processes (eg with Global Regulatory Affairs, Data Sciences).
Ensures that Client's Signal Management processes and activities are compliant with Global Health Authority expectations, including EU regulations and EU regulatory authority and inspectors’ expectations.
Represents Pharmacovigilance and Client's externally at a global level as an authoritative expert on signal detection processes.
Leads training for PSPV and other relevant functions on signal detection processes to ensure training and compliance with processes are maintained.
Leads interactions with other PSPV functions including EU QPPV and Global Medical Safety to ensure processes are regularly updated and are fit for purpose.
Leads interactions and oversight of signal management activities conducted by any vendor.
Accountabilities:
Technically fully competent to develop, review, evaluate and maintain the signal detection and management processes in line with regulations and in close liaison with the business units, including Data Sciences as well as internal PSPV stakeholders.
Leads interactions with other relevant functional areas both within and outside of GPSE to ensure standards are maintained.
Represents the pharmacovigilance department as subject matter expert in cross-functional teams or committees and external environments at a global and regional level as required.
Designs and delivers relevant training as appropriate.
Provides mentorship and guidance for junior/new pharmacovigilance scientists and others as appropriate.
Conduct project activities for designated processes.
Any other tasks assigned by manager to assist in related departmental activities.
Education &
Competencies (Technical and Behavioral):
Health care background or life science degree/Bachelors required; degree in life sciences preferred
Excellent document creation skills
In depth knowledge and experience of clinical trial methodology, pharmacovigilance regulations, signal detection and risk/benefit analysis
Critical, strategic thinking and decision-making skills
Ability to review, analyze, interpret and present complex data to a high standard
Global player in a PV organization with the ability to adapt to change
Excellent communication and presentation skills
Good level of computer literacy
Excellent organization skills and ability to prioritize