Ibrahim Khan

Clinical Project Manager with proven success delivering complex Phase I–IV trials across neurology, immunology, cardiology, and infectious diseases. Experienced in managing full study lifecycles — from start-up to close-out — including vendor selection, budgets, timelines, and regulatory compliance (MHRA, EMA).

Collaborated with leading pharma companies such as GSK, AstraZeneca, Pfizer, Vertex, and Abbott. At MAC Clinical Research, I oversee multi-site studies, ensuring projects are delivered on time and to the highest quality standards. Previously at Panthera Biopartners, I contributed to the Valneva COVID-19 vaccine trial and helped establish the UK Site Management Organisation.

BSc (Hons) in Pharmacology and Innovative Therapeutics, with GCP, IATA, and ILS training. Passionate about advancing therapeutic innovation and improving patient outcomes through high-quality research.

MAC

This role involves overseeing project direction, coordination, and implementation, ensuring alignment with company strategy. Responsibilities include leading cross-functional teams, managing project life cycles, coordinating activities, maintaining budgets, and serving as the primary contact for communication. The role also involves risk management, financial reconciliation, and participation in client meetings. Additionally, it requires adherence to health and safety policies, equality and diversity policies, maintaining professional qualifications, and following regulatory standards and data protection practices.

Panthera

As a Clinical Trial Support Officer (CTSO) at Panthera I assisted in coordinating blood sampling and processing for active clinical trials, ensuring stock control and temperature monitoring. My responsibilities include supporting Research Practitioners, liaising with stakeholders, managing data quality, and transcribing information into case report forms. I performed clinical tasks, such as blood sample collection, monitoring temperature controls, and maintaining stock control. Compliance with quality management systems, regulatory requirements, and participation in training for personal development were integral to the role.

Hvivo

As a Clinical Support Specialist at hVIVO I played a crucial role in improving population health by supporting the conduct of clinical trials focused on common viral illnesses. My responsibilities include screening subjects, performing study-specific assessments, ensuring volunteer safety, managing sample collection, and maintaining data accuracy. I also contributed to daily clinic management, temperature monitoring, and advocate for volunteers during study participation. Additionally, I assisted in planning clinic activities, liaised with recruitment officers, and provided supervision and training for ancillary staff in the screening clinical environment.

Bsc Pharmacology & Innovative Therapeutics