Mohammad Jan

Driven and compassionate clinical research professional with a passion for advancing medical research and improving patient outcomes. With a strong foundation in medicine and a desire to transition to the clinical research industry, I bring a unique perspective to the field. As an ECFMG certified international medical graduate, I am well-equipped with clinical knowledge, research experience, and excellent communication skills.

Throughout my academic and professional journey, I have gained valuable transferable skills such as attention to detail, time management, critical thinking, problem-solving, and the ability to work well under pressure. I have completed comprehensive training in clinical research methodology, study design, and regulatory compliance, and I am eager to apply this knowledge in a research setting.

My passion for the field of clinical research is driven by the opportunity to make a positive impact on healthcare by discovering and developing new treatments and therapies. I am excited to contribute my skills and knowledge to the industry and help advance the future of medicine

Clinical Research Fastrack

TransCelerate Approved GCP Training Apr 2023

ICH GCP E6 R(2)
FDA Regulations 21CFR 11, 50, 54,56 and the Common Rule 45CFR46
Data Management
Informed Consent Process
Clinical Trial Operations from feasibility through close-out.
GDP following ALCOA-C principles
Identification and reporting of AEs and SAEs
Quality Assurance, Monitoring and Query Resolution
Comprehension and Execution of Clinical Trial Protocols
Maintaining regulatory binder, housing essential documents including but not limited to 1572, DOA, Training Logs and other Investigator Site File (ISF) documentsICH GCP E6 R(2) FDA Regulations 21CFR 11, 50, 54,56 and the Common Rule 45CFR46 Data Management Informed Consent Process Clinical Trial Operations from feasibility through close-out. GDP following ALCOA-C principles Identification and reporting of AEs and SAEs Quality Assurance, Monitoring and Query Resolution Comprehension and Execution of Clinical Trial Protocols Maintaining regulatory binder, housing essential documents including but not limited to 1572, DOA, Training Logs and other Investigator Site File (ISF) documents

Skills: Federal Regulations · Electronic Data Capture (EDC) · Good Clinical Practice (GCP) · Medical Research · Institutional Review Board (IRB) · Protocol Development and Implementation · Regulatory Compliance · Clinical Study Design · Data Analysis · Data Entry · Validation Protocol · Patient Recruitment and Retention · Informed Consent · Medical Records · Team Collaboration and Leadership · Medical Terminology · Project Coordination and Organization · Presentations · Investigation · Data Collection · Clinical Trials · Case Report Forms · Clinical Research

Dow University of Health Sciences

Bachelor of Medicine, Bachelor of Surgery (MBBS), Medicine 2010-2015

Medical Graduate MD