BioCryst is a North Carolina-based biotechnology company that researches and develops novel oral therapeutics for the treatment of various diseases.

Director, Program Management (Development)

Medical Science Liaison (Northeast)

Sr. Clinical Data Manager

Biologist I Contract

BioCryst Pharmaceuticals, Inc.

Senior Staff Accountant

Accounting Consultant

Assistant Unit Controller

Branch Controller

Sr. Financial Analyst

Associate Wealth Management Advisor

Treasurer

Analyst

Finance Intern

Director, Quality Assurance

Senior Quality Specialist

Chemist

Graduate Student

Research Assistant

Assitant Researcher

Undergraduate Intern

Sr. Manager, Quality Systems, Documentation & Training

QA Manager

QA Specialist, Document Control

Accounting Manager / QA Document Control

Executive Admin / HR Assistant

Administrative / HR Assistant

Office Administrator / Accounts Payable Specialist

Senior Clinical Scientist

Senior Scientist

Clinical Scientist II

Clinical Scientist I

PhD Student in Human Movement Science

Clinical Research Coordinator

Field Medical Advisor

Field Medical Advisor - West

Field Medical Director

Senior Scientific Development Manager

Scientific Development Manager

Senior Administrative Assistant Global Development

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Director, Global CMC Regulatory

Associate Director Regulatory Affairs

Syner-G BioPharma Group provides in-depth expertise across the three key elements of Chemistry, Manufacturing, and Controls (CMC): Regulatory Services, Technical Development, and Quality/IT. We call this CMC 360™. We also provide medical writing services, with expertise in authoring a variety of regulatory documents across a wide range of therapeutic areas and in all phases of development. Our regulatory affairs services include the development and implementation of global regulatory strategic plans, regulatory agency meeting support, and electronic submissions to regulatory authorities around the world. We have the skill set and experience to guide your prime asset through any development challenges and along the ever-changing maze of regulatory filing pathways, to a position of full compliance, and high quality. Our expertise spans small molecules, peptides, oligonucleotides, biologics, monoclonal antibodies, antibody-drug conjugates, and cell and gene therapy products.

Syner-G BioPharma Group

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Microsoft Office 365

Amazon AWS

Senior Manager, Regulatory CMC

Cardinal Health is an Ohio-based healthcare company that offers services such as ambulatory care, pharmacy benefits, and in-home health management for individuals.

Project Manager, Process Excellence - Demand and Supply Planning - Nationwide

Sr Project Analyst , Process Excellence - Demand and Supply Planning - Nationwide

Warehouse Associate, Second Shift

Cardinal Health

Akamai

Amazon SES

Sendgrid

Google Cloud Hosting

Senior Scientist, Regulatory CMC

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace's mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 5,800 people across 41 countries.

Laboratory Project Coordinator

Medpace Recruitment Event - Business Administration Opportunities

Corporate Travel Coordinator

Medpace

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Pardot

Manager, Regulatory Affairs, CMC

To those who say "impossible, impractical, unrealistic," we say: "CHALLENGE ACCEPTED."Alnylam is the world's leading RNAi therapeutics company and the first and only company to bring RNAi-based medicines to market.We are developing RNAi (RNA interference) as an innovative, entirely new class of medicines to treat rare genetic, cardio metabolic, acute hepatic infectious and central nervous system (CNS) and ocular diseases.  Alnylam was founded in 2002 based on a Nobel Prize-winning breakthrough in biology – the discovery of RNAi, and a bold vision that this discovery could be used to silence disease-causing genes upstream of today's medicines. We are relentless in our pursuit of new treatments because we believe that RNAi therapeutics can be used to treat many diseases for which treatment options do not exist or are inadequate.Alnylam is turning scientific possibility into reality - in 2018, the FDA and EMA approved of our first product, ONPATTRO (patisiran) which is also the first-ever approved RNAi therapeutic. We now have four additional medicines on the market. Our robust pipeline of investigational medicines includes multiple programs in late-stage and early-stage clinical development.We are a global and diverse company of 2,000+ people. We pride ourselves on fostering a fun, inclusive and dynamic work environment where employees can recognize their fullest potential. That's why we've been named a Science Magazine Top Employer 5 years in a row ('19-'23), a Boston Globe Top Place to Work 9x in a row ('15-'23) and Fast Company's #1 Best Workplace for Innovators ('22).We are based in Cambridge, U.S., with offices throughout Europe, Asia, and South America.See our community guidelines: https://bit.ly/2FcRhJy.

Brittany Vorobeychik

Director, Global CMC Regulatory at BioCryst Pharmaceuticals, Inc.

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BioCryst Pharmaceuticals, Inc.

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