Clinical Trial Assistant (CTA)

As a Clinical Trial Assistant (CTA) at Clinogenesis Research Organisation, your role will involve supporting clinical operations and contributing to the successful execution of clinical studies. You will assist with documentation, site coordination, communication, and study tracking to ensure compliance with regulatory and study requirements. Key Responsibilities: - Maintain and update Trial Master File (TMF/eTMF) and study documentation. - Assist in preparation, review, and distribution of study-related documents (ICFs, logs, reports, etc.). - Track clinical supplies, site progress, and subject enrollment. - Support the scheduling of clinical trial meetings, monitoring visits, and training sessions. - Assist with regulatory submissions, ethics approvals, and version tracking. - Maintain trackers, spreadsheets, and study logs efficiently and accurately. - Perform data entry and ensure completeness and accuracy of study information. - Coordinate communication between clinical sites, vendors, and internal teams. - Support safety reporting and documentation as per guidelines. Qualification Required: - Candidates from all Life Science backgrounds, including: - BSc/MSc Life Sciences - Biotechnology - Microbiology - Biochemistry - Pharmacy (B.Pharm / M.Pharm / Pharm.D) - Nursing (BSc Nursing) - Biomedical Science - Medical Laboratory Technology (MLT) - Public Health - Allied Health / Biological / Health Sciences Skills Required: - Basic understanding of clinical research and medical terminology. - Familiarity with ICH-GCP guidelines (training or certification preferred). - Strong organizational and documentation abilities. - Effective communication and interpersonal skills. - Proficiency in MS Office (Word, Excel, PowerPoint).,