Principal Investigator - Durham, United States - TFS HealthScience

    Default job background
    Description

    Job Description

    Job Description

    Join Our Team as a Principal Investigator

    TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.

    About this role

    The Principal Investigator (PI) is the primary individual responsible for the ethical design and conduct of a research study including the supervision of co-investigators and study person

    As part of our SRS team you will be dedicated to one partner, an investigator-owned network of clinical research sites.

    This will be an onsite role in Las Vegas, NV

    Key Responsibilities:

    • Ensure the ethical conduct of the research study and protect the rights and welfare of research participants by complying with the IRB approved study protocol, and adhering to all University and State policies, and federal regulations, and applicable guidance
    • Supervise and ensure that all study personnel receive appropriate training, and conduct the study in accordance with the approved protocol (including approved amendments),
      Ensure that all research activities have IRB approval and other approvals required by the institution before human participants are involved, and implement the research activity as it was approved by the IRB,
    • Report any real or potential conflicts of interests of the PI or any study personnel in compliance with conflict of interest policies and management plans.
    • Obtain informed consent from participants or legally authorized representative before participants are involved in the research, and document consent as approved by the IRB.
    • Maintain written records of IRB reviews, decisions, research records and informed consent documents,
    • Obtain IRB approval for and notify the sponsor (if applicable) of any proposed change to the research protocol priorto its implementation, except when necessary to eliminate apparent immediate hazards to the participants

    Qualifications: (Max 5-6)

    • MD degree
    • Direct experience with Alzheimer's disease

    What We Offer

    We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients

    A Bit More About Us

    Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

    Our cores values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.