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Principal Investigator
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Principal Investigat....
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Principal Investigator

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1 Vacancy
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Job Location

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Durham - USA

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2784400

Join Our Team as aPrincipal Investigator

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full servicecapabilities 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 coinvestigators and study person

As part of our SRS team you will be dedicated to one partner an investigatorowned 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 prior to its implementation except when necessary to eliminate apparent immediate hazards to the participants

        Qualifications: (Max 56)

        • MD degree
        • Direct experience with Alzheimers disease

        What We Offer

        We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll 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 fullservice global Contract Research Organization (CRO) we build solutiondriven 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 decisionmaking 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.


        Employment Type

        Full Time

        Company Industry

        About Company

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