Teams at Aspire Pharma

Supports the operational delivery of pharmaceutical clinical trials and bioequivalence studies. Responsibilities include study coordination, Trial Master File maintenance, documentation quality control, compliance tracking, audit and inspection readiness, CTMS updates, vendor and stakeholder coordination, regulatory support, and cross-functional collaboration. The role also contributes to study milestone tracking, risk escalation, meeting administration, and process improvement in an ICH GCP-regulated environment.

Provides administrative and compliance support for pharmaceutical quality systems across UK and EU operations. Responsibilities include maintaining GXP and ISO-compliant QMS processes, managing training, documentation, change controls, deviations, CAPAs, validation, audits, regulatory updates, product releases, licence variations, and launch activities. The role also liaises with internal teams, vendors, and customers to implement regulatory and procedural changes and support investigations and product launches.

Reviews and oversees pharmaceutical promotional materials for compliance with MHRA, ABPI, ABHI, PAGB, and CAP codes. Coordinates final approvals with medical signatories and partner companies, maintains promotional files, verifies references, and ensures adherence to SOPs and regulatory timelines. Supports ESG activities aligned with company sustainability goals.