Internal Monitor - Projahnmo Research Foundation

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Vacancy

1

Experience

1+ years

Job Type

Full time

Salary

Negotiable

Location

Nationwide

Category

Pharmaceutical

Application Deadline: 12 Sep 2026

Published on: 26 Aug 2026

All Requirements Responsibilities Skills & Expertise Company Information

Job Description

Projahnmo Research Foundation (PRF) is looking for an Internal Monitor (Clinical Trials) to support the monitoring and quality oversight of clinical trial activities. The position involves working across Dhaka and Sylhet, ensuring that clinical trial processes, documentation, data and study procedures are conducted according to approved protocols, applicable guidelines and organizational requirements.

Requirements

Education

Bachelor of Medicine and Bachelor of Surgery(MBBS)

Additional Requirements

Age 25 to 35 years
Only Male can apply

Responsibilities & Context

Monitor ongoing clinical trial activities at assigned study sites.

Ensure study procedures are conducted according to the approved clinical trial protocol and relevant guidelines.

Review and verify clinical trial data, source documents and study records for accuracy and completeness.

Conduct regular monitoring visits and identify protocol deviations or compliance issues.

Follow up with study-site staff to resolve data discrepancies, documentation gaps and other study-related issues.

Ensure proper maintenance of essential trial documents and records.

Coordinate with investigators, research staff and other project team members regarding trial activities.

Prepare monitoring reports and communicate findings to the relevant project team.

Track corrective and preventive actions and follow up on their implementation.

Support maintenance of participant safety, data quality and overall clinical trial integrity.

Skills & Expertise

Data Analysis

Workplace

Work from office

Compensation & Benefits

Lunch Facilities

Festival Bonus

Salary Review

Lunch Facility: Full Subsidize

Festival Bonus: As per policy

Salary Review: Yearly

Requirements

Education

Bachelor of Medicine and Bachelor of Surgery(MBBS)

Experience

Minimum 1 year(s)

Age

25 to 35 years

Responsibilities & Context

Monitor ongoing clinical trial activities at assigned study sites.

Ensure study procedures are conducted according to the approved clinical trial protocol and relevant guidelines.

Review and verify clinical trial data, source documents and study records for accuracy and completeness.

Conduct regular monitoring visits and identify protocol deviations or compliance issues.

Follow up with study-site staff to resolve data discrepancies, documentation gaps and other study-related issues.

Ensure proper maintenance of essential trial documents and records.

Coordinate with investigators, research staff and other project team members regarding trial activities.

Prepare monitoring reports and communicate findings to the relevant project team.

Track corrective and preventive actions and follow up on their implementation.

Support maintenance of participant safety, data quality and overall clinical trial integrity.

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We are a professional recruiting agency connecting top talent with leading employers. Our goal is to simplify hiring through efficient and reliable recruitment solutions. We help businesses grow by finding the right people for the right roles.

Industry

Pharmaceutical

Founded

2020

Employees

31-50 employees

Location

Mirpur Model

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