Site Management Associate (Clinical Trials)
Core
Support clinical research projects by managing site communications, documents, and clinical supplies for novel medicinal products.
Role type
Site Management Associate (Clinical Trials)
Builds
Clinical trial operations and data integrity for novel medicinal products
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
dashboards & analysis
Required skills
Site management, document management, clinical supply chain, regulatory submissions, payment administration, audit coordination, EDC monitoring, CTMS management, translation oversight, safety information flow
Preferred skills
Administrative experience in clinical research, international environment experience
Technologies
CTMS, EDC, Trial Master File (TMF), Investigator Site File (ISF), MS Office
Responsibilities
Exchange data and documents between sites, vendors, and project teams; manage clinical supply inventory and reconciliation; coordinate regulatory and ethics committee submissions; administer site and vendor payments; prepare for and follow up on audits and inspections; monitor EDC completion; maintain tracking systems and TMF; ensure safety information flow.
Seniority
Entry-level to Junior, hands-on support role