We take the time to understand your business, your values and the type of employees you want to hire.
We understand the complexity involved in hiring competent professionals especially in the Pharmaceutical and Biotech Industry.
Our sourcing teams mine our own vast and growing database of exceptional talent, by accessing areas that no one typically takes the time or resources to seek out.
Our in-depth interviews go beyond the standard answers to discover if an individual’s skills, experience, personality and motivation are suited to your company.
Our aim is to save you valuable time and money by presenting you with the most qualified candidates and helping you to close the deal using the best practices throughout the offer and negotiation process.
We follow through with complete candidate on boarding, including reference checks, background screening and logistical co-ordination.
If you want to gain access to specialized professionals or increase control over costs, contract candidates are the answer. Most companies have broadened their hiring strategies to include contract employees.
We have a deep pool of qualified contractors that span the industry.
Our recruiters will find and place contractors that have the capability to integrate seamlessly into your team at your premises.
Our contractors will help you meet a tight deadline, or provide long-term support on a vital project.
Most importantly our contractors can provide the expertise you need from day one and they always hit the ground running.
PharmaBio Staffing specializes in providing project development teams and senior consultants within the Pharmaceutical, Biologics, Generics, Medical Devices and OTC industries.
Our consultants have varying levels and areas of expertise which they utilize to achieve maximum results with greatest efficiency.
Your requirements are our consultant’s primary focus and their focus is always to work towards creating solutions that can sustain long term stability and are scalable.
From an hour’s work with one consultant to major projects involving a large team of consultants, we can assist in providing the correct solution for you.
We provide product development system support to the Pharmaceutical, Biologics, Generics, Medical Devices and OTC industries.
This includes clinical data integration solutions, clinical trial master file and regulatory submissions, and compliance support.
We use state of the art software systems to organize and automate your regulatory, clinical trial data and compliance documents including systems for full integration and analytics for your clinical data, eTMF automation to eCTD submission capabilities.
We use an innovative data collation and review platform for your clinical trial data. With this, we can provide risk-based monitoring and analytics to avoid potential issues in trial conduct and critical data.
We provide regulatory and compliance submission services support to meet your regulatory and submission needs.