Related skills
gcp edc oncology ms project etmfπ Description
- Independently lead full-service clinical projects (Ph I-IV) in oncology.
- Oversee timelines, scope, cost, and quality across global trials.
- Coordinate cross-functional teams and external stakeholders.
- Manage client relationships, proposals, budgeting, and delivery.
- Travel domestically and internationally as required.
- Drive study execution and risk/QA across trial phases.
π― Requirements
- Degree or life science qualification, or equivalent.
- 5-7 years CRO/global PM for full-service trials.
- Oncology trial experience.
- GCP/ICH knowledge and clinical development process.
- Travel ability; strong English and presentations.
- Proficiency with MS Office, MS Project, CTMS, eTMF, EDC, IXRS.
π Benefits
- Collaborative, high-energy team environment.
- Focus on work-life balance and professional growth.
- Equal opportunity employer with inclusive culture.
- Global remote work with travel opportunities.
- Privacy policy and data protection emphasis.
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