Job Description

Roles and Responsibilities: Provides Qualifications and Agreements by: Maintaining current, up-to-date curriculum vitae. Maintaining current licensure to practice. Demonstrating the proper education, training and experience to conduct the clinical investigation. Assuming responsibility for the conduct of the clinical investigation. Ensures Protocol Compliance by: Possessing a thorough understanding of the requirements of each protocol. Determining that inclusion / exclusion criteria are applicable to the study population. Ensuring recruitment goals are reasonable and attainable. Reviewing the inclusion / exclusion criteria, schedule of visits, end point criteria and investigational article use with the research team. Manages the Medical Care of Subjects by: Assessing subject compliance with the test product and follow-up visit. Assessing subjects response to therapy. Evaluation of adverse experiences. Ensuring that medical care is provided to a subject for any adverse event(s) that is reported. Informing a subject when medical care is needed to treat an inter-current illness(es). Protects the Rights and Welfare of Subjects by: Ensuring that the informed consent form contains all the elements required. Obtaining a signed and dated informed consent from the subject or subjects legal representative prior to initiation of any study-related procedures. Informing the subject or legal representative about all aspects of the clinical trial. Ensures Documentation of Study-Related Procedures, Processes and Events by: Conduction of physician examination as per the protocol and applicable procedures for volunteers. Documenting deviations from the approved protocol. Documenting that informed consent has been obtained from the subject or legal representative. Documenting adverse event(s). Complying with written procedures to document changes to data and / or case report forms. Maintaining trial documents as required by the regulations and sponsor for the appropriate timeframe and under secure conditions. Maintains Professional and Technical Knowledge by: Attending education workshops. Reviewing professional publications. Participating in professional societies. Other responsibilities as assigned by the DGM-Clinical Operations / Principal investigator from time to time. Desired Candidate Profile can send to email: hr@qpsbioserve.com Note: Opening for 2 Male physician