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Added 20 mins ago
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Centre for Chronic Disease Control

Project Technical Support – I

Delhi, ON, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 8, 2026
Positions available: 1
Posting language: English
Posted: Oct 10, 2026

Original job description

Number of Positions: 1

Location: Delhi/NCR and other project sites if required

Organization Name: Centre for Chronic Disease Control (CCDC)

Organization Proﬁle: Centre for Chronic Disease Control (CCDC) is a not-for-proﬁt research organization engaged in knowledgegeneration and knowledge translation for the prevention and control of non-communicable (chronic) diseases in varied settings of developing countries. CCDC has been recognized as a Scientiﬁc and Industrial Research Organization (SIRO) by Department ofScientiﬁc & Industrial Research (DSIR), Ministry of Science and Technology, Government of India. CCDC also holds recognition asa WHO Collaborating Centre for Surveillance, Capacity Building and Translational Research in Cardio-metabolic diseases and isan ICMRCollaborating Centre of Excellence.

Project Brief: The PURI-HF trial is supported under the joint funding window of NIH and ICMR (RO1 grant) involving air puriﬁers toassess its impact on heart failure outcomes. The primary recipients of the grant are NYU and AIIMS with CCDC being a technical collaborator. The role is to conduct the exposure assessment, procurement of equipments, management of the trial data, conductfollow up and support with patient engagement

Job Description

Role Overview: The PTS-1 plays a critical role in the successful ﬁeld implementation of the PURI-HF Study. Serving as theprimary link between the research team and the local community, this role focuses on participant enrollment, clinical tracking,hardware instruction, and data integrity under the direct supervision of the Project Manager.

Key Roles And Responsibilities

Participant Recruitment & Retention

Enrollment & Motivation: Visit randomly selected households to educate and motivate eligible community members to participate in the research trial.
Proactive Follow-ups: Manage scheduled follow-up timelines, trace hard-to-reach participants, and actively work to minimize loss-to-follow-up rates.
Patient Navigation: Coordinate logistics and personally guide participants to partner healthcare institutions (AIIMS / Medanta) for specialized clinical testing.

Data Collection & Field Research

Structured Interviewing: Conduct detailed, baseline, and annual interviews using standardized study questionnaires.
Qualitative Assistance: Assist senior research staﬀ in conducting qualitative In-Depth Interviews (IDIs) and Focus Group Discussions (FGDs).
Clinical Assessments: Perform objective ﬁeld tasks, including taking accurate anthropometric (height, weight) and basic clinical measurements.

Puriﬁer Counseling & Patient Support

Equipment Training: Deliver clear, empathetic orientation and counseling to enrolled households regarding the correct usage and maintenance of air puriﬁers.
Results Disbursal: Hand-deliver laboratory test reports to study participants, explaining basic timelines and ensuring all receipts are formally documented.

Data Integrity & Reporting

Secure Data Entry: Log all ﬁeld survey responses, tracking logs, and follow-up metrics into the project database with high accuracy.
Conﬁdentiality: Maintain strict data protection protocols to ensure participant privacy and trial ethics are never compromised.
Progress Reporting: Compile and submit comprehensive weekly progress reports directly to the Supervisor or Project Manager.

Responsibilities And Requirements

Essential: 1+1 + Diploma (MLT/DMLT/ITI 01 1) DMLT/Research/ equivalent) + two years’ Experience i1 ﬁeld work Experience relevant Subject/ﬁeld

or

Three years Graduate degree in relevant subject/ﬁeld+ one year experience in relevant subject

or

Candidates possessing a Post-Graduate (PG) degree in the relevant discipline shall be deemed full eligible for recruitment against PTS-1 and PTS-II positions without requiring any mandatory work experience.

or

The additional higher qualiﬁcation (Master’s Degree) acquired beyond the minimum prescribed educational requirement (Bachelor’s Degree) will be treated in par with the required experience

Desirable

DMLT/Research/ equivalent) + two years’ Experience, 1 ﬁeld work Experience in diﬀerent Public Health projects, in a government, autonomous, PSU, recognized organization

Application Process Information

Kindly submit your application by mentioning your details and attaching your CV in this form. Last date for sending your application is 19th October 2026. [Only shortlisted candidates will be contacted for the interview].

Compensation: Remuneration will be as per ICMR norms commensurate with experience andqualiﬁcations.

CCDC envisions to reduce chronic disease burden and promote innovative science that has the potential to improve human health through implementation and translational research.

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More about this job

Responsibilities

Recruit and retain study participants, conduct interviews and field assessments, coordinate clinical visits, and provide guidance on air purifier use. Enter and protect study data, document report delivery, and submit weekly progress reports.

Requirements

Applicants must meet one of the stated education and experience pathways, including a relevant diploma with two years of relevant experience or a relevant graduate degree with one year of experience. A relevant postgraduate degree qualifies candidates without mandatory work experience; experience in public health projects is desirable.

Skills

Participant Recruitment
Participant Retention
Community Engagement
Patient Navigation
Structured Interviewing
Qualitative Research
Anthropometric Measurements
Basic Clinical Measurements
Air Purifier Training
Data Entry
Data Integrity
Confidentiality
Follow-Up Coordination
Progress Reporting

Visa sponsorship

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Keywords

PURI-HF Study
Heart Failure
Air Purifiers
Exposure Assessment
Clinical Research
Public Health
Non-Communicable Diseases
Participant Enrollment
Participant Retention
Household Visits
Follow-Up
Patient Navigation
AIIMS
Medanta
Baseline Interviews
Annual Interviews
Standardized Questionnaires
In-Depth Interviews
Focus Group Discussions
Anthropometric Measurements
Clinical Measurements
Laboratory Test Reports
Research Data Management
Data Protection
Trial Ethics
Field Research

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