Biography

Barrister Rajin Ahmed, a member of the Honorable Society of Lincoln’s Inn, is an Advocate of the Supreme Court of Bangladesh and a distinguished expert in aviation law, legislation drafting, and international contracts. With extensive experience in representing corporations, government entities, and non-profits, he has played a pivotal role in drafting key aviation laws, including the Civil Aviation Act (2017) and the Carriage by Air (Montreal Convention) Act (2020).

Rajin Ahmed was instrumental in improving Bangladesh's ICAO audit compliance to 75.34%, exceeding regional and global averages. He is an active member of esteemed legal associations such as the Inter-Pacific Bar Association and the International Air & Transport Safety Bar Association. A skilled litigator and regulatory advisor, he also teaches aviation law as an Adjunct Faculty at BSMRAAU.
His areas of practice span corporate law, dispute resolution, and constitutional law, showcasing his versatility and international recognition.

Job Responsibilities

• Legal Compliance: Ensure all IRB activities adhere to local and international laws, including FDA, ICH-GCP, and ethical guidelines.
• Contract Review: Draft, negotiate, and review legal agreements, including investigator contracts and confidentiality agreements.
• Policy Development: Advise on and develop standard operating procedures (SOPs) for the IRB to ensure ethical research practices.
• Regulatory Guidance: Provide legal opinions on regulatory requirements impacting clinical trials and human subject research.
• Ethical Oversight: Evaluate protocols to ensure compliance with ethical standards for the protection of trial participants.
• Conflict Resolution: Mediate and address conflicts of interest or ethical concerns related to clinical trials.
• Training and Awareness: Conduct legal and ethical training sessions for IRB members and research staff.
• Document Management: Oversee legal documentation, including informed consent forms and compliance reports.
• Risk Mitigation: Identify and address legal risks in clinical trial operations and IRB activities.
• Liaison Role: Collaborate with sponsors, investigators, and regulatory agencies on IRB-related legal matters.