QPS Bioserve Released Job Openings On 27/01/2023.QPS was founded in 1995. Today, the company is considered one of the top CROs in the world. QPS is a GLP/GCP-compliant contract research organization (CRO) supporting discovery, preclinical and clinical drug development. QPS provides quality services to pharmaceutical and biotechnology clients worldwide.
Vacancy Details:
QPS Bioserve Recruiting MBBS in Medicine Candidates with 00 Years Experience for Physician Position.Complete Details for the Physician follows.
Important Details :
- Location : Hyderabad/Secunderabad
- No of Vacancies:NA
- Details of Salary:Not Disclosed
- Opening date for online Application: 27/01/2023
- Mode of application :Online
- How To Apply: Interested can send to email: hr@qpsbioserve.com
Related Job: Sai Life Sciences Looking For FRESHERS And Experienced
For more Latest pharma jobs https://pharmapage.in/
Job Description/Skills Required
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:
Click here for Official notification and Apply
