Project Nurse -III - ICMR TOF-SPAR-DM Project

St John's; Bengaluru; On-site; INR 345,000 - 488,000; Full time

Job summary

St John's in Bengaluru, Karnataka seeks a Project Nurse III to support the ICMR TOF-SPAR-DM Project. The nurse will screen participants, obtain informed consent, coordinate visits, collect samples, and counsel participants throughout the study period.

The role requires data capture in REDCap after training, monitoring during visits, and ensuring timely completion of study procedures with good participant retention.

Qualifications

• Four-year nursing degree (B.Sc. Nursing) with a minimum of second class or CGPA, or GNM with Post Basic B.Sc. Nursing/equivalent.
• Age 35 years.
• Experience: Fresher / 2–3 years in clinical or research settings.

Responsibilities

• Screen eligible participants for the study and obtain informed consent.
• Coordinate and assist participants during scheduled follow-up visits.
• Collect blood and other study samples as per protocol.
• Provide patient counselling and address study-related queries.
• Record patient-reported outcomes and enter data in REDCap after training.

Skills

English

Kannada

Telugu

Tamil

Hindi

Education

B.Sc. Nursing or GNM with Post Basic B.Sc.

Tools

REDCap

Job description

Project Nurse -III - ICMR TOF-SPAR-DM Project

Employment Type: Contract

Experience: 4 years in Nursing

Job Summary:

The nurse will assist in patient screening, enrolment, informed consent procedures, follow-up visits, sample collection, patient counselling, and monitoring during the study period. The patient reported outcome measures will also be coordinated by her/him. Responsibilities also include coordinating patient visits, assisting in adverse event reporting. The Project Nurse will play an important role in patient care, participant retention, and timely completion of study-related procedures throughout the project duration. He/she will capture data in the redcap after requisite training.

Salary : Rs. 36,400/- pm

No of Vacancy :One

Key Responsibilities:

• Eligible participants in the study.
• Assist in explaining the study and obtaining informed consent from participants.
• Coordinate and assist patients during scheduled follow-up visits.
• Collect blood and other required study samples as per the study protocol.
• Provide patient counselling and address routine study-related queries.
• Coordinate and record patient-reported outcome measures during the study.
• Monitor participants during study visits and inform the study team of any concerns or changes in their condition.
• Assist in identifying, documenting, and reporting adverse events and other safety-related issues.
• Maintain regular contact with participants and help ensure that they attend their scheduled visits.
• Enter study-related data in REDCap after receiving the required training.
• Maintain accurate and timely study records and ensure that all required procedures are completed as per theProject

Eligibility Criteria:

Preferred Qualifications:

Four-year nursing course (B.Sc. Nursing) with a minimum of second class or equivalent CGPA from a recognized institute, or GNM with Post Basic B.Sc. Nursing/equivalent in many project notifications

Age Criteria : 35 Years

Experience : Fresher / 2–3 years of clinical or research experience

Preferred Language: English, Kannada, Telugu, Tamil, Hindi

Tentative Date of Joining :15th October 2026