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Highly meticulous Clinical Research Associate with a strong ability to oversee and organize various operational tasks, supervise sites effectively, and compile comprehensive clinical reports. Extensive expertise in the clinical trial process, ICH/GCPs, and FDA Regulations, complemented by a background in laboratory research regulatory compliance and program management. Proficient in action planning, maintaining database security, ensuring compliance with standard operating procedures, and managing programs. Committed to diligently monitoring and protecting the well-being and rights of clinical trial patients.

Motivated Life Sciences graduate and GCP-trained professional with an advanced diploma in clinical research. Possesses strong foundational knowledge of ICH-GCP guidelines, clinical trial documentation and TMF management. Eager to leverage exceptional organizational skills and medical terminology proficiency to support data accuracy and compliance as a Clinical Trial Assistant.

Doctor of Pharmacy graduate with four years of experience in clinical research and the pharmaceutical industry. Seeking a challenging position that offers professional career growth in the pharmaceutical industry and related sectors.
Specialized in literature surveillance, data entry for case processing, and aggregate reporting. Proficient in performing literature reviews, triage, case processing, narrative writing, aggregate reporting, and signal activities. Hands-on experience with drug safety databases, including Oracle Argus Safety database and MedDRA/WHO dictionary.
• Skilled in global safety databases such as ARGUS and ARISg.
• Prepared case narratives following CIOMS or MEDWATCH guidelines, focusing on medically relevant adverse event information.
• In-depth knowledge of local and global regulations, policies, and procedures related to adverse event collection and reporting.
• Proficient in ICSR reconciliations and vendor reconciliations.
• Effective communication skills with excellent verbal and written abilities.
• Strong organizational skills, detail-oriented, and adaptable to change.
• Attentive to detail, a team player, and proactive in taking initiative.

To obtain a challenging role in Pharmacovigilance, where I can use my skills, ability to work with details and precision in providing relevant services Adaptable professional with a quick-learning ability and a talent for adjusting to new environments. Skilled in rapidly acquiring new knowledge and applying it effectively. Driven by a passion for continuous learning and successfully navigating change.

Dr. Hasanath Jahan

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Homeopathic Consultant

Medical Coding Officer

Chief Medical Officer

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Master's degree - Public Health

Diploma of Education -

Bachelor's degree - Homeopathic Medicine

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Master's degree - Public Health

Medical Coding Officer

Diploma of Education -

Homeopathic Consultant

Chief Medical Officer

Bachelor's degree - Homeopathic Medicine

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