Jobs at OPIS s.r.l.

Maintain the electronic Trial Master File by uploading, indexing, QCing, and archiving study documents. Review documents for quality and compliance, support Document Owners, resolve documentation issues, respond to Sponsor queries, provide status updates, train new staff, and ensure the eTMF is inspection-ready.

The Business Development Associate will identify and engage potential clients, research decision-makers in the pharma sector, coordinate meetings, and maintain CRM data to nurture client relationships.

The Junior Programmer will develop, maintain, and optimize web applications and clinical databases, support integrations, and ensure compliance with quality standards.

Manage SOPs and controlled/Sponsor documents in the QMS, conduct compliance reviews and audits, support GCP/GxP quality activities, CAPA, supplier qualification, training coordination, and monitor KPIs/KQIs to ensure regulatory compliance and continuous improvement.

Prepare, analyze, and deliver high-quality RFP responses and budget proposals for clinical research projects. Coordinate with internal stakeholders, maintain RFP archives, suggest pricing strategies, ensure compliance/confidentiality, and support the Head of Proposal Management to produce competitive proposals.