Global Clinical Operations Coordinator
hace 2 semanas
About the Role
As a Study Delivery Specialist at Pharmiweb, you will be part of the world's largest and most comprehensive clinical research organization, driven by healthcare intelligence.
Key Responsibilities
- Support the clinical trial team at the global level, impacting project success.
- Stay up-to-date with ICH GCP, sponsor standards, and attend relevant training sessions.
- Manage study trackers, access, and analysis of reports, ensuring timely distribution to the study team.
- Provide system-related support, including TMF Management and Maintenance, and stakeholder follow-up for improved compliance.
- Collaborate with SDS/SM to manage post-SAC activities and archival support.
Requirements
- Excellent technical/IT skills, with the ability to understand technology's impact on studies.
- Knowledge of ICH GCP, operational procedures, systems, and quality guidelines.
- Ability to work independently and as part of a team, with a professional attitude and good customer focus.
- Strong time management skills, with a high English language proficiency.
- 1-2 years of experience in clinical operations, with knowledge of main systems (vTMF, mCTMS).
What We Offer
- A competitive salary and a range of benefits, including various annual leave entitlements, health insurance options, and a global Employee Assistance Programme.
- Opportunities for professional growth and development in a diverse and supportive culture.
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