Henna Nisar

Clinical Development and Clinical Data professional with an MSc in Stem Cells & Regenerative Medicine and 9+ years across global biopharma, CROs, and NHS environments. Experienced in supporting Physicians and Clinical Science Directors through high-quality data review, interpretation, protocol-aligned documentation, and decision-ready insights. Brings a strong foundation in clinical trial methodology, life sciences research, ICH-GCP, and regulatory expectations, combined with NHS system knowledge and real-world understanding of mental-health pathways.

Skilled in synthesising complex clinical and operational data into clear narratives that support study strategy, risk assessment, and scientific decision-making. Recognised for structured communication, cross-functional collaboration, and the ability to work autonomously in fast-moving, remote environments.

Carer & Small Business Owner - Self-Employed - Wakefield, UK

(2024-11)

Provided full-time care for a family member with schizophrenia and psychosis, gaining deep insight into mental-health pathways, crisis escalation, medication adherence, and multidisciplinary coordination. Developed high-empathy communication, resilience, and advocacy skills while navigating NHS services. Alongside caring responsibilities, founded and operated a home-based bakery business, managing customer engagement, marketing, pricing, and service delivery - strengthening commercial awareness and operational discipline.

• Authentic understanding of mental-health challenges and service gaps
• High-empathy communication and rapport-building
• Commercial mindset and customer relationship management
• Operational planning, problem-solving, and self-directed working

Clinical Audit Manager - NHS England - Remote

(2024-08 - 2024-11)

Delivered audit oversight across multiple clinical programmes, ensuring alignment with national policy, governance frameworks, and regulatory expectations. Led structured review of Real-World Data (RWD) inputs and outputs to ensure accuracy, traceability, and readiness for senior decision-making.

• Designed streamlined audit reporting frameworks improving clarity and reducing delays
• Partnered with clinical, governance, and quality teams to implement CAPAs
• Applied advanced search logic to interrogate disparate systems and validate evidence
• Ensured outputs were regulator-ready and supportive of strategic decisions

Senior Clinical Data Analyst - Parexel - Remote

(2020-12 - 2024-03)

Provided senior oversight for global clinical studies across multiple therapy areas. Led data cleaning, validation, reconciliation, and scientific review to ensure analytical and regulatory integrity. Acted as SME for EDC platforms and supported cross-functional teams with data interpretation.

• Developed advanced Boolean search strategies to surface high-risk data
• Served as SME for EDC platforms, training global teams
• Harmonised data review workflows to improve consistency and inspection readiness
• Ensured analytical outputs accurately reflected upstream data inputs
• Managed stakeholder communication and deliverables
• Supported Physicians and Clinical Scientists with data interpretation, identification of clinical trends, and preparation of decision-ready summaries
• Contributed to protocol-aligned documentation, including data review plans, listings, and scientific narratives

Assistant Clinical Trial Manager - DePuy Synthes (Johnson & Johnson)

(2019-10 - 2020-12)

Supported operational management of clinical studies, ensuring alignment with protocols, monitoring plans, SOPs, and regulatory expectations.

• Coordinated investigator sites, vendors, and internal teams
• Improved eTMF structure, indexing, and document traceability for audits
• Supported vendor and research site oversight and quality review checkpoints
• Contributed to successful audits and inspections
• Primary contact for investigators and internal stakeholders
• Assisted in preparing study documentation, including protocol-aligned materials and inspection-ready records

Clinical Project Manager - MediNova Research

(2019-06 - 2019-10)

Directed multi-site clinical trials, overseeing site performance, vendor deliverables, and timelines. Synthesised operational and clinical data into concise reports for sponsors.

• Established standardised project plans and optimised vendor management processes
• Maintained sponsor relationships through structured communication
• Facilitated global stakeholder meetings, improving collaboration

Clinical Coder & Medical Summariser - NHS North Leeds Medical Practice

(2019-03 - 2019-06)

Reviewed and summarised large volumes of unstructured clinical records, ensuring accuracy, consistency, and downstream usability.

• Conducted quality checks on patient records and documentation
• Supported GPs by resolving queries on medical records

Cancer Pathway Coordinator - Bradford Royal Infirmary (NHS)

(2018-01 - 2019-03)

Coordinated complex cancer pathways across MDTs, ensuring timely escalation of risks and accurate pathway data.

• Coordinated patient pathways to ensure timely access to diagnostics and treatment
• Liaised with clinical teams to monitor progress and address delays
• Supported MDT meeting preparation with accurate patient data
• Collected, tracked, and reported pathway data to support service improvement
• Engaged with patients to provide support and education

MSc - Stem Cells & Regenerative Medicine - University of Chester

BSc - Biomedical Sciences - University of Bradford