Dr Golam Kabir

Provided medical management and expertise for clinical trials, contributing to study reports, regulatory documents, and manuscripts. Acted as the internal medical expert, reviewing, presenting, and interpreting results in Clinical Study Reports.

Executed medical review of case reports, including narrative/coding review and causality assessment. Performed safety surveillance activities for investigational medicinal products and authored/reviewed aggregate reports.

Provided leadership and direction to medical and clinical staff during clinical studies, overseeing study-specific medical duties and screening functions. Ensured adherence to Good Clinical Practice (GCP) and managed medical aspects of subjects within studies.

Fulfilled roles as Sub Investigator and Principal Investigator, ensuring subject safety and adherence to ICH-GCP guidelines. Conducted patient assessments, managed adverse events, and contributed to study documentation and ethics submissions.

Assessed and treated chronic and acute medical conditions and injuries, determining fitness for detention, release, and interview in custody. Performed forensic examinations, including intimate body searches and documentation of injuries.

Assessed physical and mental conditions affecting work capacity, analyzing medical evidence to produce reports for the Department of Work and Pension. Conducted home visits and trained new colleagues on assessment guidelines and practices.

Examined and recruited candidates for various programs. Contributed to the selection process of prospective students.

Provided medical care as a Locum Clinical Research Physician in early phase pediatric studies. Contributed to research activities and patient management.

Managed medical needs of study volunteers, recording adverse reactions and serious adverse events, and updating CRFs. Wrote and edited documents for ethics committee and MHRA submissions, serving as the primary contact for volunteers.

Lectured Master of Science students on clinical trials and drug development, covering background, informed consent, and regulatory requirements. Provided real-life examples, including case studies of clinical trial outcomes.

Organized clinical work placement experiences for aspiring medical students. Recruited and examined candidates for various programs.

Served as a Research Physician and Co-Investigator, contributing to clinical trials. Participated in study design and execution.

Provided clinical assistance in the Diabetes Clinic. Supported patient care and medical operations.

Completed a clinical attachment in Stroke and Acute Medical Ward. Gained experience in patient care and ward management.

Performed research technician duties, supporting various clinical studies. Assisted with data collection and laboratory procedures.

Provided translation and interpretation services for various needs. Facilitated communication between different language speakers.

Lectured and taught students at the university. Developed and delivered course content.

Focused on advanced studies in diabetes, covering its pathophysiology, diagnosis, and management. Gained expertise in clinical research methodologies relevant to diabetes care.

Undertook comprehensive coursework in biotechnology, exploring molecular biology, genetic engineering, and bioprocess technology. Developed skills in laboratory techniques and scientific research.

Completed a comprehensive medical degree, covering foundational medical sciences, clinical practice, and patient care. Prepared for a career in medicine and surgery.

Completed a postgraduate diploma in bioinformatics, focusing on the application of computational tools to biological data. Acquired proficiency in analyzing genomic and proteomic information.