Clinical Research Associate – Taipei Taiwan jobs at Msd in Taiwan
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Track (e.g. essential documents) and report (e.g. Safety Reports). Ensure collation and distribution of study tools and documents. Update clinical trial databases (CTMS) and trackers. Clinical supply & non-clinical supply...
Ownership of country and site budgets. Development, negotiation and completion of ClinicalTrial Research Agreements (CTRA). Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout. Oversees FCPA, DPS/OFAC, and...
Oversee the review, escalation, negotiation, and approval of site budgets and payments. Lead or participate in regional and global improvement projects related to Study Start Up and other processes involving...
Develops strong site relationships and ensures continuity of site relationships through all· phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP,· Sponsor SOPs, Local Laws...
Track (e.g. essential documents) and report (e.g. Safety Reports). Ensure collation and distribution of study tools and documents. Update clinical trial databases (CTMS) and trackers. Clinical supply & non-clinical supply...
Trial and site administration:o Track (e.g. essential documents) and report (e.g. Safety Reports)o Ensure collation and distribution of study tools and documentso Update clinical trial databases (CTMS) and trackerso Manage...
The Associate Supply Chain Manager is responsible for coordinating and managing the end-to-end supply chain activities of the organization. They collaborate with multiple internal and external stakeholders to ensure the...
Track (e.g. essential documents) and report (e.g. Safety Reports). Ensure collation and distribution of study tools and documents. Update clinical trial databases (CTMS) and trackers. Clinical supply & non-clinical supply...
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