Join our dynamic team and lead the charge in supporting AstraZeneca's Development pipeline from a bioanalytical perspective. You'll manage bioanalytical operations for pre-clinical studies and clinical trials, ensuring timely delivery of quality data by coordinating activities between multiple stakeholders.
Key Responsibilities:
Vendor Management: Support the team contracting with third-party lab service providers for assay development and validation. Collaborate with business operations, procurement, and clinical teams to ensure appropriate SOWs and contracts.
Study Coordination: Manage critical reagent supply and sample analysis. Work closely with bioanalytical strategy leads, clinical trial teams, and lab service providers to finalize study documents and meet timelines.
Documentation & Data: Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs). Drive the delivery of data transfer specifications and ensure data accuracy.
Sample Logistics: Track and reconcile sample testing, resolving any issues that arise.
Qualifications:
Education: BA/BS in a scientific degree + 2 years’ experience in a Bioanalytical laboratory.
Experience:
Experience of working in a regulated environment
Understanding of clinical trial design
Skills:
Strong organizational and analytical skills.
Excellent written/verbal communication.
Ability to work both independently and as part of a team.
Proficiency with Excel and other interactive programs.
Why Join Us?
Innovative Environment: Work on cutting-edge projects in a collaborative setting.
Professional Growth: Opportunities for learning and development.
Impactful Work: Contribute to life-changing clinical trials and research.
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