AstraZeneca Pharmaceuticals LP Clinical Project Manager - 12 Month Contract in Macquarie Park, Australia
Clinical Project Manager
12 Month Fixed Term Contract
At AstraZeneca we lead our industry in our development of a strong and varied pipeline. This means our people are here to win. We give you a breadth of opportunities to be curious and do cutting edge, unique work that has big impact on science and medicine.
This couldn’t be more true for our Clinical Research team. Our Clinical Research team are responsible for ensuring that study activities are being carried out in accordance with local and global procedural and regulatory requirements as we look to bring our products to market in a timely manner.
As our new Clinical Project Manager, you will be responsible for effective study management across a number of high profile studies. This is a broad role where you will be responsible for all aspects of the study from start-up through to close-out. You will work closely with an experienced team focused on delivering best outcomes for AstraZeneca and our patients.
Main Duties and Responsibilities
Overall responsibility for study commitments from start-up through to close-out, ensuring timely delivery of high quality data
Lead Australian Study Delivery Team through proactive patient recruitment, risk identification/mitigation and study site progress
Lead and optimise the performance of the Local Study Teams, consisting of monitors and study administrators, at country level ensuring compliance with ICH-GCP and AZ Procedures
Perform any required co-monitoring & QC visits with study monitors
Report study progress/strategy to AZ global colleagues.
Assist in forecasting study timelines, resources, recruitment, budget, study materials and drugs.
Attend and contribute to global or national Investigator meetings.
Ensure study is ‘inspection ready’ at all times through proactive management of essential documentation.
Liaise and collaborate with AZ medical and commercial colleagues to deliver the R&D pipeline
Experience working in a similar capacity, with proven track record in proactive study management
University degree in related discipline, preferably in life science, or equivalent
Fluent knowledge of spoken and written English.
Excellent interpersonal and communication skills, along with good negotiation skills and a demonstrated ability to work effectively in a team environment.
A strong focus on quality, with an excellent knowledge of international guidelines ICH-GCP
Strong prioritisation, problem solving and time management skills
Ability to respond quickly to changing priorities and opportunities
Highly proficient in computer programs and clinical trial management systems
Ability to travel nationally as required. Occasional International travel may also be required.
Full working rights (we are not able to sponsor for this role).
Experience in Oncology would be beneficial but not essential
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.