• Clinical Research Associate

    Insight Global (New Haven, CT)


    Job Description

    A client of Insight Global is looking for Clinical responsibilities include collecting clinical data and biological samples such as ECGs, vital signs, and venipuncture in accordance with study protocols and standard operating procedures. Accuracy checks are performed regularly, and source documentation is maintained diligently. Adverse events are monitored and promptly reported to medical staff. Research participants are guided and supported ethically and safely throughout their involvement. Visual examinations are conducted, and diagnostic devices are operated as needed. Biological samples are managed with care, including labeling, documentation, and inventory reconciliation. Participant intake is handled via phone, with a focus on maintaining database integrity. Ongoing clinical training is attended, and certifications are kept up to date to ensure compliance and quality care.

     

    We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

     

    Skills and Requirements

     

    2-3 years of experience in Clinical Research Trials

     

    2-3 years of experience in Data Collection or Clinical Trials Assistant

     

    Experience with GPD (Good Documentation practices)

     

    Proficiency with MS Teams