Senior Data Professional

3 days ago


Brisbane, Queensland, Australia beBeeData Full time $100,000 - $130,000

At Avance Clinical, our people are the foundation of our success. We foster a collaborative and dynamic work environment that values teamwork and respects individual contributions.

Our company specialises in providing services supporting clinical drug development for the pharmaceutical and biotechnology industry.

We seek an experienced Data Manager with passion for data management in a clinical research setting, eager to work in a stimulating environment where expertise matters.

The successful candidate will be responsible for capturing and documenting clinical research data as per the study protocol. They will collaborate with colleagues to ensure accurate and secure data collection, management, and reporting.

This is a permanent full-time position, which can be worked home-based from anywhere in Australia or home or office based in Adelaide.

Key responsibilities include:

  • Preparation of Data Management Plans
  • Preparation or review of Edit Check Document
  • Development and review of Case Report Forms (CRFs) and completion guidelines in line with the database and protocol
  • Preparation of clean and erroneous dummy data
  • Database Validation (testing data entry screens and edit checks using dummy data)
  • Provide training to site, Sponsor, and other staff in the use of eCRF systems
  • Resolution of Quality Assurance (QA) comments
  • Perform data review and cleaning of data collected during the trial
  • Perform Quality Control on study data prior to lock
  • Act as Data Project Manager including interaction with Clinical Project Manager, interact with site/client/external vendors, perform overall Project Management, and timeline management

To succeed in this role, you will need:

  • An ordinary degree in the appropriate discipline or equivalent experience
  • A minimum of 2 years' experience in the pharmaceutical industry/CRO working in a GCP environment
  • Experience with Medrio and/or Medidata Rave is desirable
  • Knowledge of ICH GCP Guidelines, medical terminology, and clinical trials process
  • Experience in EDC/e-CRF systems
  • Intermediate MS Office Suite

We offer a reputable growing organisation with stability, a challenging and stimulating environment where expertise matters, a diverse and inclusive culture with strong team collaboration, comprehensive training, and attractive remuneration.

Benefits

Competitive salary package and benefits

Opportunities for career growth and professional development

Collaborative and supportive work environment

Flexible work arrangements and work-life balance

Requirements

Proven experience in data management in a clinical research setting

Strong knowledge of ICH GCP Guidelines and medical terminology

Proficient in EDC/e-CRF systems and MS Office Suite

Ability to work collaboratively as part of a team

About Us

Our company is a leading provider of clinical drug development services for the pharmaceutical and biotechnology industry.



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