Clinical Data Manager

DM310124_1706680521 Posted: 31/01/2024

• AU$75000 - AU$90000 PER ANNUM
• Sydney, New South Wales
• Permanent

Company Overview: Join a dynamic and rapidly growing US Medical Technology company at the forefront of innovation. From humble beginnings in startup mode, they are now on the verge of a groundbreaking milestone - first patient for a Chronic Implant Study. As they expand their presence in Australia, we are seeking a passionate and skilled Data Manager to join the dedicated team.
Key Responsibilities:

• Manage and oversee data for clinical trials, ensuring accuracy, completeness, and compliance with regulatory requirements.
• Utilise expertise in Medrio software for efficient data management processes.
• Collaborate with cross-functional teams to support the successful execution of clinical trials.
• Maintain a keen focus on data quality, identifying and resolving discrepancies in a timely manner.
• Contribute to the development and implementation of data management processes and SOPs.
• Ensure adherence to regulatory standards and guidelines related to clinical trial data.

Requirements:

• 1-2 years of experience in a Data Manager role.
• Proven work experience within a Clinical Trial environment.
• Expertise in using Medrio software for data management.
• Strong understanding of regulatory compliance in clinical trials.
• Excellent attention to detail and the ability to work effectively in a fast-paced environment.
• Demonstrated ability to work collaboratively in a remote setting.
• Flexibility to be based anywhere in NSW or QLD.

Preferred Qualifications:

• Familiarity with other data management tools or software.
• Experience in therapeutic areas related to medical device technology.

Why Join Us:

• Be part of a pioneering team on the brink of a major milestone

i-Pharm Consulting is a specialist Recruitment Company servicing the global Pharmaceutical industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Executive Consultant Dana Sarkissian on or email dsarkissian@i-pharmconsulting.com