Of all our jobseekers who reach final interview stage for a regulatory affairs role, 95% will get an offer. And 98% of these will accept it.
An exciting opportunity has come up to assist the client going through a phase of growth and we need to get the right amount of talent in quickly to ensure the quality of work doesn’t lapse.
The Pharmacovigilance Consultant / QPPV. will be responsible for the preparation, management scheduling and submitting reports to health autotities. You will be the responsible person for all AE escalation.
Excellent opportunity to un the delivery of PV and Drug Safety services along ICH-GCP guidelines, regulatory requirements and Client SOPs/project process within a very well respected consultancy
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81% of survey respondents want a job with some degree of flexibility. It's an absolute must for talent attraction and retention.
With the deadline for the implementation of CDISC standards fast approaching, we look at what this means for the industry.
Hydrogen’s David Chen joined an esteemed panel to discuss pharmacovigilance and the need for greater transparency.