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. QPS India was established in 2004 and is located in Hyderabad, India. QPS offers a broad range of Clinical Services in compliance with applicable regulatory and ethical guidelines.
- Vacancy details:
- Department : Jr.Executive – Quality Assurance
- Qualification: B.Pharma,M.Pharma
- Experience – 0 years
- Salary: ₹ Not Disclosed
Job Description: Greetings from QPS Biserve India Private Limited. ...!!
- Important Details :
- Location: Hyderabad( Balanagar )
- Post of date:05/06/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Walkin Interview Details:
Job description
Administration of Investigation drug products to the study subjects.
- 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 volunteers documents are compiled and available for the check-in activity.
- Coordinate for subject enrollment process during check-In and end of the study.
- 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 dos and dons 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.
Preferable for Male candidates
M/s QPS Bioserve India Private Limited
plot 47, IDA Balanagar
Hyderabad
Near Balanagar ‘X’ roads
Walk In Interview : 23-May-2024 & 24-May-2024 | Next Week- Monday to Friday
Desired Candidate Profile: 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.
1). Female – 1 No
2). Male – 2 No
