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KLINEXA is a scientifically focused contract research organization that provides pharmaceutical, biotechnology and medical device companies with a full range of services.

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  • Pharmacovigilance Compliance & Training Associate

    Pharmacovigilance Compliance & Training Associate - Incyte Department: Pharmacovigilance Location: Wilmington, DE Under the leadership of the Manager, Pharmacovigilance (PhV) Compliance and Training, this position provides support in evaluating the quality and compliance of the PhV organization through established training and … Continue reading

  • Medical device Medical Writer

     Med device Medical Writer with CER exp Contractor can sit in Raynham, MA , Westchester UK or Warsaw, IN Division: Medical Operations 12-24 months Job Function Summary Overview: The Medical Writer responsible for preparation of documents that support the presentation … Continue reading

  • Proofreader, Global Labeling Deliver

    Proofreader, Global Labeling Delivery Gaithersburg, MD 12-36 months The Labeling Operations Proofreader is responsible for supporting development and implementation of new and revised printed labeling for assigned products, primarily in a proofreading capacity. Depending on ability, the candidate may also … Continue reading

  • Clinical Data Analyst

    Clinical Data Analyst is responsible for CTMS and Grants Manager study build, maintenance, and support activities. RARITAN, NJ 12-24 months   • Work with Study Teams and partners during study build process to create/maintain the following in CTMS: o Study, … Continue reading

  • Regulatory Affairs Manager

    Regulatory Affairs Manager multiple positions  ** Please make sure that all candidates have a min of 2 years of industry (pharma or CRO) experience doing submissions within reg affairs Gaithersburg, MD 6-36 months Description- Prepare and deliver regulatory operational plans for … Continue reading

  • Network Qualification Engineer

    Job Summary Our Client is seeking a Network Qualification Engineer for a contract position.  The successful candidate will perform IT infrastructure activities for a medium sized network using best practices in life science industry, author qualification related documents, review company … Continue reading

  • Research Associate, In-Vivo

    Job Summary Our client is looking for a self-motivated and quality focused individual to join our In-Vivo team.  The successful candidate will work hand in hand with our study directors, veterinarians, quality assurance and sponsors/clients to ensure all study aspects … Continue reading

  • Clinical SAS developer

    Location: Raritan, NJ POSITION SUMMARY: To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS: (Core Responsibilities – 1. Develop and document programs to create analysis datasets summarizing key clinical trial data. 2. Develop and document programs … Continue reading

  • Clinical Research Associate

    Location: Grayslake, IL Your Project Coordinator skills are needed just about anywhere. But is it where you want to go? Imagine working for one of the nation’s most respected companies. Making a strategic contribution. Receiving the rewards and recognition you … Continue reading

  • Chemist

    Location: MO This individual will be responsible in doing wet chemistry within a lab setting. Looking for candidates who have experience working hands on at the bench level. Apply today! Job Description- The position is to do “wet chemistry” in … Continue reading