We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.
Who are we?
- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence
- 20+ years of experience, 450+people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe
- Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trial
- We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, cardiovascular and chronic diseases to improve the health of millions worldwide.
- Our profits support our parent organisation – The George Institute – a medical research institute with a mission to Improve the Health of Millions of People Worldwide
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Why work with us?
- We are a global team, making a social impact – we are a unique profit-for-purpose CRO that support a not-for-profit health organisation
- Competitive market salary and benefits
- Flexible and agile working arrangements – onsite, hybrid or WFH (dependent on location)
- Strong and diverse Learning & Development opportunities including exposure to scientific
- A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities and other fun events!
About the role:
The Senior Clinical Data Manager will work closely with Data Management, Clinical Operations and Project Management teams within George Clinical.
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Key responsibilities:
- Ensuring quality and accuracy of research data
- Where appropriate, take on project management role for assigned projects
- Liaison with project staff (Research Fellows, Division Heads, Project Managers, external parties) to determine data collection and reporting requirements
- Designing, or assisting in the design of electronic data collection systems
- Designing, or assisting in the design of Case Report Forms or other data collection tools
- Maintaining systems for data collection
- Participate in the development and validation of new data management systems and processes as necessary
- Designing and generating data reports
- Mentor, train and supervise data management staff
- Project planning and planning resources
- Interact with clinical, programming and statistics project leads and other project team members
What are our expectations of candidates?
- Tertiary qualifications in science or related field
- Approximately 6 years of increasing responsibility in data coordination of clinical trials.
- Strong IT skills including SQL, reporting software, all MS Office applications, web-based databases and the Internet, and strong conceptual ability to learn new software applications quickly. Experience with statistical packages is desired but not essential.
- Proven ability to handle large data sets, including reporting and other evaluation procedures
- A strong understanding of relevant Good Clinical Practice, NHMRC and TGA regulatory guidelines, especially as connected with data quality and accuracy
- Ability to evaluate and recommend changes to existing processes and procedures for greater effectiveness
- Excellent time management and project management skills
- Excellent written and verbal communication skills
- High level problem solving, analytical, and strategic thinking skills
- Excellent interpersonal skills and the ability to work well and flexibly ie. autonomously, in small teams and with a wide range of varying stakeholders, including senior management
- Technological proficiency including Microsoft Office packages
- Ability to see the big picture, yet still focus on detail and quality of work
- Ability to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments
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We are searching for individuals who are excited by the idea of regional and global projects and teams, don’t want to get lost in a large CRO and are ready to have their ideas heard!
You will be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence.
How do I apply and what if I’m interested in a role in future or want to refer someone?
Apply via LinkedIn or send your CV, referral or confidential query to careers@georgeclinical.com and our friendly HR team across the world will reach out as appropriate soon. Please provide your full contact details, the location you are applying for, whether you are interested in a current or future opportunity and we’ll be in touch. We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.
How do I learn more about the roles and George Clinical?
Follow us on Linkedin to see our regular updates and how we celebrate our people and success across our business and projects! You can also visit us at www.georgeclinical.com.
We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.
Thank you for your interest in working with George Clinical. As a global business, we are committed to handling Personal Information in accordance with applicable privacy and data protection laws in the many countries in which we do business. Please see our Privacy Policy for further information.
