Role Overview

We are seeking a motivated and detail-oriented Clinical Research Fresher to join our team. The ideal candidate will assist in the planning, execution, and monitoring of clinical trials while ensuring compliance with regulatory requirements and Good Clinical Practices (GCP). This is an excellent opportunity for individuals aspiring to build a career in clinical research.

Key Responsibilities

Trial Preparation and Support

Assist in the preparation of trial protocols, case report forms (CRFs), and other study-related documentation.
Coordinate site initiation visits and other study start-up activities.

Monitoring and Compliance

Monitor clinical trial sites to ensure adherence to study protocols, GCP guidelines, and ethical standards.
Verify the accuracy of study data through source document verification.

Documentation and Reporting

Maintain study files and ensure proper documentation for audits.
Assist in preparing study progress reports and presentations.

Collaboration

Work closely with investigators, site staff, and clinical teams to resolve study-related issues.
Support data management teams in resolving discrepancies.

Training and Development

Participate in GCP, regulatory, and protocol-specific training sessions.
Stay updated with the latest guidelines and developments in clinical research.

Qualifications and Skills

Educational Background:

Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field (mandatory).
Master’s degree in Clinical Research or relevant certifications (preferred).

Key Skills:

Basic understanding of clinical trial phases and regulations (ICH-GCP, FDA, EMA).
Strong organizational and communication skills.
Proficiency in Microsoft Office Suite and data management tools.
Attention to detail and ability to manage multiple tasks efficiently.

Clinogenesis Research Institute remote jobs

Clinical Research Fresher