Job summary
Job post source
This job is directly from Premier Research
Job overview
The Consultant role at Premier Research involves providing expert regulatory guidance to biotech, medtech, and specialty pharma clients to help bring innovative medical products to market.
Responsibilities and impact
The Consultant will offer regulatory advice across therapeutic areas, navigate complex regulatory landscapes, consult to enhance service offerings, and contribute specialized knowledge to clinical trials while working flexibly on aligned projects.
Experience and skills
Candidates need a BS in a science-related field with 3+ years as a Regulatory Project Manager or equivalent, prior FDA experience, expertise in Neuroscience, Pediatrics, Rare Disease, or Women's Health, and advanced knowledge of US and international regulatory requirements.
Career development
Premier Research supports growth by providing skills and opportunities for career advancement with flexibility and work-life balance.
Work environment and culture
The company values employee input, flexibility, and collaboration, emphasizing a supportive environment built for biotech innovation.
Company information
Premier Research specializes in regulatory affairs for biotech, medtech, and specialty pharma, focusing on transforming scientific breakthroughs into medical products.
Unique job features
The role offers flexibility to work on projects matching expertise and availability, contributing to meaningful clinical trials in specialized therapeutic areas.
Company overview
Premier Research is a global contract research organization (CRO) specializing in providing clinical development services to the biotechnology, pharmaceutical, and medical device industries. They make money by offering comprehensive clinical trial management, regulatory consulting, and data analysis services that help clients bring new therapies to market efficiently. Founded in 2002, Premier Research has a strong history of focusing on complex and rare diseases, leveraging their therapeutic expertise and innovative approaches to support the development of life-changing treatments.
How to land this job
Position your resume to emphasize your regulatory expertise, especially your experience working directly with the FDA and managing regulatory projects in clinical research.
Highlight your knowledge in critical therapeutic areas such as Neuroscience, Pediatrics, Rare Disease, or Women's Health, showcasing your ability to navigate complex regulatory landscapes.
Apply through multiple platforms including Premier Research's official corporate career site and LinkedIn to maximize your chances of visibility and consideration.
Connect with current employees or consultants in Premier Research's Regulatory Affairs division on LinkedIn; open conversations by referencing recent regulatory changes, asking about team culture, or expressing genuine interest in their therapeutic area expertise.
Optimize your resume for ATS by incorporating keywords from the job description such as 'Regulatory Project Manager,' 'FDA experience,' 'global regulatory pathways,' and specific therapeutic areas to pass initial automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and find relevant LinkedIn contacts, allowing you to focus your energy on interview preparation and networking.
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