Netherlands Job Openings
BeiGene
Senior Study Start-up Specialist
FULL TIME
November 25, 2024
- Responsible for start-up activities in Netherlands and provides local expertise.
- Identify gaps and areas for improvement and propose CAPA.
- The Start-up specialist is responsible for collaborating closely with the Regional Clinical Operations Manager/Start-up Lead to ensure study timelines are adhered to and required quality standards are maintained.
- CRA experience is considered a plus
- Provide country-specific study start-up expertise, assist on start-up activities, provide support in budget and contract negotiations
- Retrieves essential documents from study site and performs essential document site file reconciliation. Perform independent quality review of submission packages, submit package to EC (and HA), if required.
- Review and translate drug labels, ICF, site specific recruitment materials and other applicable documents.
- Manages sites and site performance by tracking regulatory submissions and relevant milestones
- Ensure inspection readiness of start-up study and site documentation
- Collaborates with Regional Clinical Operations Manager/ Start-up Lead and clinical study sites to ensure timely delivery of start-up milestones
- Evaluates the quality and integrity of site practices – escalating quality and/or GCP issues with Investigators and internal team as appropriate.
- Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating excellence, question status-quo and promote innovation.
- Mentor and manage junior SSU staff
- Acts as the escalation point person for SSUS(s) with site related issues and concerns
- May serve as subject matter expert for clinical operations, country regulations and SSU-related activities.
- BS in a relevant scientific discipline and 2 years of Start-up experience.
- Experience in oncology global trials preferred
- Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
- 2-5 years of Start-up experience in the pharmaceutical or CRO industry
- Excellent communication and interpersonal skills
- Excellent organizational skills and ability to prioritize and multi-task
- Fluent in English and Dutch (writing and speaking)
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
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