Clinical Research Coordinator; Fresher

Position: Clinical Research Coordinator (Fresher)
Clinical Research Coordinator (Entry-Level / Fresher)

Company:  Clinogenesis Research Organization

Role Overview

At Clinogenesis Research Organization, the Clinical Research Coordinator (CRC) supports the planning, coordination, and execution of clinical research studies under the supervision of the Principal Investigator (PI). The role involves assisting with participant management, maintaining accurate study documentation, collecting and managing clinical trial data, and ensuring that all research activities comply with study protocols and regulatory guidelines.

Roles and Responsibilities

Assist in coordinating and implementing clinical research studies according to approved protocols at Clinogenesis Research Organization.

Schedule and manage study participant visits and maintain participant records.

Screen and identify potential participants based on study inclusion and exclusion criteria.

Assist in the informed consent process and explain study procedures to participants when required.

Collect, record, and maintain accurate clinical trial data in Case Report Forms (CRFs) and electronic systems.

Maintain and organize study documentation, regulatory files, and essential trial documents.

Ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Support the Principal Investigator and research team during study procedures and monitoring visits.

Track study materials, investigational products, and research supplies as required.

Report adverse events, protocol deviations, and other study-related information to the research team.

Assist in preparing documentation and reports for monitoring visits, audits, and inspections.

Education Qualification

Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Nursing, Clinical Research, M pharma , B pharma , BDS , BHMS , D pharma

Required Skills

Basic knowledge of clinical research processes and clinical trials.

Understanding of Good Clinical Practice (GCP) and regulatory guidelines.

Strong organizational and documentation skills.

High attention to detail and accuracy in data collection and reporting.

Good communication and interpersonal skills to interact with study participants and research teams.

Ability to manage time and coordinate multiple study activities.

Basic computer proficiency, including MS Office and data entry systems.

Ability to work effectively in a collaborative team environment.