Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Bioanalytical Study Manager

Role Overview:

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 environmentUnderstanding of clinical trial designSkills: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.

Apply Now and Make a Difference in Bioanalysis!