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SalaryCDM_1706683031 Posted: 31/01/2024
- Sydney, New South Wales
- Permanent
A new opportunity to join a specialist life-science business, working with cutting-edge technology and methodologies. Providing an opportunity to work with the latest industry technology and stay up-to-date with advancements in the field.
As a growing business, tailored progression opportunities are offered to suit individual needs with direct support from senior management to ensure healthy growth in the team.
You will be joining a collaborative smaller team environment and given the full scope of responsibility of managing all data management activities, supporting the project leads, in a hands-on and client facing role.
This role will be based in their Sydney office.
Suitable for an experienced Clinical Data Manager with experience in a CRO or similar setting, able to work in a fast-paced environment.
Key Responsibilities:
The Clinical Data Manager will be responsible for managing all aspects of clinical trial data from study start-up through database lock. This includes developing and implementing data management plans, designing case report forms, overseeing data entry and validation, and generating study-specific data reports. The ideal candidate will be a detail-oriented, self-starter who can work independently and collaboratively in a fast-paced, small company environment.
- Develop and implement data management plans for clinical trials
- Design case report forms (CRFs) and review/edit CRFs created by CROs or study teams
- Manage electronic data capture (EDC) systems and oversee data entry and validation
- Ensure data quality and accuracy by conducting data review and query resolution
- Create and review data reports for clinical study team and regulatory submissions
- Perform database lock and archiving activities in accordance with SOPs and regulatory requirements
- Contribute to the development and improvement of data management processes and procedures
- Collaborate with cross-functional study teams to ensure timely and accurate data collection and reporting
- Bachelor's degree in a relevant scientific discipline (e.g., biology, chemistry, statistics) or equivalent experience
- Minimum of 2 years of experience in Clinical Data management, preferably in a CRO environment
- Knowledge of ICH/GCP guidelines and FDA/EMA regulations
- Experience with EDC systems and CRF design
Location: Melbourne (hybrid offered)
Salary: $80,000 - $120,000 plus superannuation (dependent on experience)
Do not hesitate to apply if you are interested. Please send your CV to Keeley Munday at kmunday@i-pharmconsulting.com 02 8310 5854 or apply direct to this link for a further confidential discussion.
