01Responsibilities
Work under minimal guidance and participate in the conduct of clinical research reputed company and protocols, contributing technical and clinical expertise.
Contribute to the execution of clinical trials in terms of reputed company operational aspects of study start-up through reputed company-out including supplying study materials to sites.
Participate in the preparation of clinical study specific training materials, as needed.
Support the administration of clinical studies according to good clinical practices (GCP) and reputed company operating procedures (SOPs), which may include management of communications with contract vendors, CROs, clinical study team, and clinical sites.
Review study documentation for accuracy and completeness in accordance with protocol, GCP, and regulatory requireme
