Research Clinical Specialist

Abiomed is a pioneer and global leader in healthcare technology and innovation, with a mission of **Recovering Hearts & Saving Lives**. With corporate headquarters in Danvers, Massachusetts, offices in Aachen & Berlin, Germany and Tokyo, Japan, Abiomed’s 1,400 employees form one of the fastest growing medical device companies in the world. We attract and...

TITLE: CLINICAL SALES MANAGER Why is the position open? Expansion QUALIFICATIONS: Bachelor’s degree - four-year degree from accredited reputable institution Start-up company experience selling disruptive technology A minimum of 8 years of experience within sales, sales management, and/or training or marketing organization is required High level of...

The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...

Are you ready to #BeEpista? At Epista, you will grow a career in a setting that cherishes curiosity, integrity, and development. Epista Life Science is dedicated to defining and delivering process, technology and compliance excellence. Since our founding, we’ve expanded into multiple countries with big ambitions for the future. Our team is our superpower -...

Essential Job Duties: - Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance (as per the training status of the CRAI-MEA); liaise with vendors; and other duties, as assigned - Responsible for aspects...

**Essential Job Duties**: 1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of...

With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced US Regulatory Affairs Lead to join the Autolus team to expand their cell and gene therapy products in the United States (US). Key Responsibilities - To provide strategic US regulatory input into clinical development and ensure the development and...

**Location**: - US - East Coast**Job Summary**: Job Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced US Regulatory Affairs Lead to join the Autolus team to expand their cell and gene therapy products in the United States (US). Key Responsibilities - To provide strategic US regulatory input into...

The Senior CRA is responsible for site monitoring and site management. Responsibility for clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA assures the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume line...

Conduct installation, troubleshoot and repair, test and qualify equipments located at assigned sites - Provide professional and timely coverage to customers within 24 hours of notification - Schedule and manage installation and preventive maintenance (PM) activities as well as conduct unscheduled visits at sites - Determine correct inventory levels of spare...