Senior PV Process Scientist
- Interim/Contract
- PVG & Drug Safety, Clinical Drug Safety
This vacancy has now expired. Please see similar roles below...
Hobson Prior are currently working with a global pharmaceutical organisation who are seeking a Senior PV Process Scientist to join them on a contract basis in Hertfordshire or Basel. Our client focuses on researching and developing novel medicines and marketing them once they have been developed.
Job Responsibilities:
- Support the Global Head and the Leaders of Scientific Enablement and Processes in completing identified tasks and deliverables in connection with routine support provided to various teams in respect to the core PDS processes and scientific enablement.
- Assist in the completion of projects and new strategic initiatives by managing logistics, integrating with teams, attending meetings, and following through on assigned tasks.
- Triage, and organize requests for Scientific Enablement and Processes support from the wider organization (PDS and other functions).
- Expand the reach of the Global Head and the Leaders of SEP and the group's overall effectiveness by maintaining contact/dialogue with key stakeholders (e.g. within PDS, with cross-functional teams (e.g. GDTs, LCTs) and/or working groups) already established by the SEP group and to triage and disseminate new requests to maximize SEP involvement.
- Contribute in the development of new tools under the leadership of the Global Head and the Leaders of Scientific Enablement and Processes.
- Support the quality management of the core PDS processes under the supervision of the PV Process Leader and in collaboration with other stakeholders.
- Keep up-to-date of new developments in the core PDS processes to have proper context in support of the PV Process Leader and successful completion of assigned tasks.
Key Skills:
- Ability to operate effectively in a multifunctional, matrix team.
- Fluent in English (verbal and written).
- Excellent written and verbal communication skills.
- Attention to detail -good prioritization and organization skills.
- Good computing/IT skills.
Requirements:
- MSc or a degree in a life science or healthcare-related discipline (e.g. PharmD, nursing, dentistry, etc.).
- Relevant experience in pharmacovigilance and/or a clinical safety-related role (typically 3+ years of experience).
- Familiarity with one or more core PDS processes (e.g. ICSR management, signal management, risk management) and/or other critical supportive processes (e.g. benefit-risk assessment, aggregate reporting, etc).
- Familiarity with regulatory pharmacovigilance requirements and guidelines published by the major global Health Authorities (e.g. FDA, EMA, MHRA, etc).
- Experience in project management is admirable.
Apply now:
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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