Project Technical Support -III - ICMR BLUE SHOCK Trail Project
St. John’s Research Institute · Bengaluru · onsite · Posted 29d ago
Undisclosed3–8 yrsfulltimeSourced from
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About this role
Bedside and technical support for trial conduct across the Medical and Surgical ICUs, including:
- Daily screening of ICU admissions for septic shock and assistance in identifying eligible patients within the 24-hour enrolment window.
- Assisting the investigators in the informed consent process and in maintaining consent documentation.
- Prospective bedside collection of clinical, hemodynamic and laboratory data at the predefined time points - vasopressor doses, MAP, cardiac output and SVR, lactate, ABG and organ-support parameters.
- Operating and assisting with cardiac output monitoring devices as per standardized protocols; escalating technical faults promptly.
- Collection, labelling, processing, aliquoting, storage and transport of blood samples for biomarker (IL-6, procalcitonin) and routine laboratory analysis, and liaison with the central laboratory.
- Accurate and timely completion of case record forms and data entry into the study database; correction of queries raised during data validation.
- Follow-up of enrolled participants for outcome data up to day 28, including record retrieval and telephonic follow-up where required.
- Maintaining study logs, drug accountability records, sample inventories and consumable stock.
- Reporting any suspected adverse event immediately to the Project Research Scientist-I and the Principal Investigator.
- Assisting in study documentation, filing and audit preparation, and any other technical task assigned by the Principal Investigator in connection with the project.
Preferred Qualifications:
Essential:
- Graduate degree in Science / Life Sciences / Nursing (B.Sc. Nursing) / Medical Laboratory Technology / Allied Health Sciences from a recognized university with 3 years of relevant experience; OR
- Post-graduate degree in a relevant subject (Life Sciences, Microbiology, Biochemistry, Biotechnology, Clinical Research, Allied Health Sciences) from a recognized university.
- Training or certification in Good Clinical Practice.
- Experience with phlebotomy and sample processing, and familiarity with ICU monitoring equipment.
- Proficiency in computer applications, data entry and electronic data capture systems (MS Excel, REDCap or equivalent).
35 Years
Preferred Language
English
Disclaimer: This job posting and location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
CGMPaudit preparationelectronic data captureclinical researchICUCardiacmeanphlebotomyrefractoryBiotechnologyMicrobiologyBiochemistryIntravenousResearchAdmissionsData EntryexcelData ValidationLife Sciences
About St. John’s Research Institute
St. John’s Research Institute
Education & Training
1001-5000
employees
2004
22 years old
Bengaluru, Karnataka
India
₹4.6L PA avg
Avg at St. John’s Research Institute
About
The St. John's Research Institute (SJRI) is a part of the St John's National Academy of Health Sciences, which is run by the CBCI Society for Medical Education. From its inception, St. John's has set before it an ideal of excellence in academic courses as well as service to society as a result of which it has truly become holistic both in its outlook and in its approach to the problems of community health.
In 2000, the Academy decided that its commitment to excellence in research required the setting up of an Institute that was dedicated to the pursuit of research and capacity development in St. John's. This vision encompassed improvement of health of the community and patients through research and development of a Center for Excellence in medical research in India.
The Institute was formally inaugurated in September 2004 by His Eminence Cardinal Telespore Toppo.
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