Clinical Trial Monitor

Clinical Trial Monitor (Entry Level)

Role Summary :

Assist in clinical trial monitoring activities to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory standards. Support senior CRAs in reviewing data, managing documentation, and coordinating with clinical trial sites.

Key Responsibilities :

Assist with remote or on-site monitoring visits.

Verify Case Report Form (CRF) entries with source documents.

Maintain and update Trial Master File (TMF / eTMF).

Track patient recruitment, study supplies, and milestones.

Identify and report missing data, deviations, or errors.

Coordinate with investigators, site staff, and study teams.

Support in safety reporting and regulatory documentation.

Eligibility :

Candidates from any Life Science background, including :

BSc / MSc Life Sciences

Biotechnology

Microbiology

Biochemistry

Pharmacy (B.Pharm / M.Pharm / Pharm.D)

Nursing (BSc Nursing)

Medical Laboratory Technology (MLT)

Biomedical Science

Public Health

Zoology / Botany / Genetics

Chemistry / Biology / Food Science / Allied Health Sciences

Skills Required :

Basic understanding of clinical trials and medical terminology.

Knowledge of ICH-GCP guidelines (training preferred).

Strong communication, documentation, and analytical skills.

Proficiency in Microsoft Office tools.

Preferred (but not mandatory) :

GCP certification

Internship or short clinical research training