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The Senior Specialist will develop regulatory strategies and manage deliverables, liaising with various stakeholders while ensuring compliance and team coordination.

The Pharmacovigilance Project Manager will oversee project management activities, liaise with clients, ensure service quality, prepare project reports, and manage expectations.

The PV Project Manager will oversee project activities, manage client expectations, prepare project scope, and report progress to stakeholders while ensuring quality in pharmacovigilance services.

The Clinical Research Associate II monitors clinical trials, ensuring investigator facilities and staff meet study requirements, supports regulatory submissions, and trains site staff as needed.

The PV Project Director manages and supports Project Managers in delivering pharmacovigilance activities on time and within budget, ensures compliance with regulations, and maintains client relationships while overseeing team performance and development.

The PV Associate supports ICSR management, processes reports, manages safety events, and liaises with clients under supervision while ensuring compliance with regulations.

Lead the ICSR management team, ensuring task distribution, overseeing workflows, and maintaining client cooperation, while also managing ICSR staff and monitoring performance.

The role involves managing clinical projects in early phase oncology, ensuring timely delivery, training team members, and maintaining quality standards while facilitating project meetings.

The Freelance Clinical Project Manager will oversee bid defense activities, manage project communications with sponsors, ensure timely delivery within budget, and facilitate project meetings. Early phase oncology experience is essential, alongside Mandarin fluency.

Ergomed seeks a Freelance Clinical Project Manager fluent in Mandarin with early phase oncology experience to oversee project activities and ensure delivery standards.