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Proclinical is seeking a Project Manager to lead and coordinate clinical studies across all phases and lifecycle stages. In this role, you will work collaboratively with cross-functional teams to ensure timely delivery of study objectives while managing risks, challenges, and budgets effectively.
Job Responsibility:
Provide end-to-end leadership of clinical studies in compliance with SOPs, ICH-GCP, and relevant local regulatory requirements
Own study level deliverables, proactively partnering with cross functional stakeholders to resolve operational risks, challenges, and execution issues
Ensure patient safety, data integrity, and inspection readiness through robust quality management systems and adherence to company metrics
Act as a primary sponsor partner, supporting delivery against study assumptions while mentoring and developing junior team members
Lead study set up and documentation activities, including protocol authoring and clinical study report (CSR) development
Conduct and oversee feasibility assessments to identify and select suitable investigational sites
Manage sponsors, vendors, and internal/external teams to ensure on-time, high quality trial delivery
Requirements:
Degree or equivalent experience in healthcare or a relevant discipline
Background working as a CRA
Strong understanding of ICH GCP, ISO 14155, and regulatory requirements
Ability to adapt to changing project deliverables and escalate issues as needed