Related skills
ms office gcp edc ich ms project📋 Description
- Lead clinical projects within budget and scope; may run international trials.
- Serve as primary client liaison for service quality, proposals and presentations.
- Liaise with project team and senior management including C level.
- Lead all aspects of one or more clinical trials.
- Oversee data management, safety, clinical, medical monitoring and biostatistics.
- Prepare status updates with key deliverables and success metrics.
- Contribute as an active project team member to improve trial management.
- Prepare and review study docs such as project plans, informed consents, site contracts and budgets.
🎯 Requirements
- Degree or life science qualification, or equivalent.
- Experience in full-service/global PM in CRO.
- 5-7 years industry; 4+ years PM in CRO trials.
- Experience managing Oncology studies.
- GCP/ICH knowledge and clinical development process.
- Ability to travel domestically and internationally.
- English proficiency; strong presentation skills.
- Proficient in MS Office, MS Project, PowerPoint; CTMS/EDC/eTMF/IXRS.
🎁 Benefits
- Supportive, collaborative team culture.
- Focus on work-life balance and development.
- Opportunity to work on Oncology trials globally.
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