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QPS Bioserve India Walk In 16th & 17th May 2022 for B.pharma,M.pharma Freshers & Experienced

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QPS Bioserve India Pvt Ltd Walk In Interview 2022  B.Pharma/M.pharma for Clinical Research Executive At Hyderabad/Secunderabad( Balanagar ). QPS Bioserve India Pvt Ltd Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.

  • Vacancy details:
  • Post Name: Clinical Research Executive
  • Qualification: B.Pharma/M.pharma       
  • Experienced:0 to 1 years
  • Openings:NA
  • Salary:NA

Job Description: QPS Bioserve India Pvt Ltd Hiring For Clinical Research Executive !

  • Important Details :
  • Location: Hyderabad/Secunderabad( Balanagar )
  • Walk In Date:16th May – 17th May 
  • Time:10.00 AM – 4.30 PM
  • Venue:QPS Bioserve India Private Limited, Plot No: 47, 2nd Floor, Beside Obulam Insulators Near Balanagar Bus Stop, Balanagar, Hyderabad – 500 037 Ph No: 040 6837 5555
  • Contact – Gayatri Battina ( 04068375555 )
  • Note:Interested applicants with eligible qualification can send their profiles to [email protected] and can also walk in to below address with profiles and academic documents.
  • Post of date:13/05/2022
  • Selection Process: The selection will be on the basis of Interview.

Job description

  • Ensures that feasibility and readiness of the clinical unit, emergency unit and equipment’s for conduction of the study activities.
  • Ensures that regulatory related documents, approved Protocol and Informed consent forms etc., are available with the Trial Master File.
  • Arrangement of all study related documents as per the protocol requirements.
  • Ensures that the all study related volunteer’s documents are compiled and available for the check-in activity.
  • Coordinate for subject enrollment process during check-In and end of the study.
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  • Performed the study related activities as per GCP, Principles and ethics, the applicable regulatory requirements, protocol and its amendments.
  • Obtained and documented the informed consent in compliance with the applicable regulatory requirement(s), GCP and ethical principles.
  • Training the subjects on do’s and don’ts during the study.
  • Coordination with investigator and coordinators for drug administration activity.
  • Administration of Investigational drug products to the study subjects.
  • Coordination with the clinical staff for drug administration, sample collection, vitals checking and processing etc., is performed according to the protocol.
  • Reporting of adverse events to investigator / physician for adverse event management.
  • Coordination with the dietician for standardized diet distribution as per the study protocol.
  • Ensures all withdrawals and dropouts of study subjects are reported to the Coordinators.
  • Ensures subject compliance to all the study related activities.
  • Ensures timely and accurate transcription of data from the source documents

About Company:

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.

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