Work as Associate Director Project Data Manager at AstraZeneca

AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

Post : Associate Director Project Data Manager

Job Description
Accountabilities
As an Associate Director Project Data Manager, you will provide CDM leadership for assigned projects, indications and/or studies dependent on size and scale of the project. You will take global accountability and serve as the second line of contact at the project level. Your responsibilities will include strategic planning and delivery of CDM deliverables at project level, management and oversight of vendor contracts, resourcing and budget management, and oversight of vendor performance for assigned projects and studies. You will also be responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology.

Candidate Profile :
• University or college degree in the life sciences or related subject, pharmacy, nursing or equivalent relevant degree.
• Ability to successfully manage simultaneous trials and meet deadlines.
• Significant Clinical Data Management experience, preferable both from CRO and Pharma industry in more than one therapeutic area.
• Excellent understanding of clinical trials methodology, GCP, GDMP and medical terminology.
• Comprehensive knowledge of clinical standards, e.g. SDTM or CDASH.
• High attention to detail and a strong analytical mind-set.
• Demonstrates a comprehensive knowledge of database structures and of capturing and storing clinical information as they apply to CRF design, database development, data handling and reporting.
• Excellent interpersonal skills and proven ability to operate effectively in a global environment.
• Good written and verbal communication skills, negotiation, collaboration, conflict management and interpersonal skills.
• Cultural awareness.
• Experience of CRO and vendor management.
• Experience as a lead of a large Phase III trial or multiple smaller trials;
• Knowledge of SQL, 4GL, VBA or R software
• Experience of managing teams.
• Experience with Regulatory Inspections
• Project Management training.

Additional Information
Job Location : Bangalore
Qualification : University or college degree in the life sciences or related subject, pharmacy
Industry Type : Pharma / Healthcare / Clinical research
End Date : 20th June 2024