Associate Clinical Data Manager
at IQVIA
Sydney, New South Wales, Australia -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 07 Aug, 2024 | Not Specified | 09 May, 2024 | N/A | Database Design,Technology Solutions,Clinical Data Management,Training,Medical Terminology,Data Science,Clinical Trials | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Currently seeking a Associate Clinical Data Manager or Sr Clinical Data Coordinator to join the Data Management team in Australia. This role can be based anywhere in Australia and offers remote working. You will love all things data with a strong EDC background in clinical trials or hospital setting. You will be able to work independently and part of the wider team. SAS experience would be an advantage but not essential.
SKILLS AND EXPERIENCE REQUIRED:
- Bachelor’s degree or educational equivalence in clinical, biological or mathematical sciences or related field OR a nursing qualification or equivalent combination of education, training and experience.
- Robust understanding of medical terminology and jargon required.
- At least 3 years of relevant experience in clinical data management.
- Strong EDC experience in clinical trials coupled with DM queries (familiarity with EDC platforms).
- SAS experience is not required, although good to have (database design).
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.co
Responsibilities:
- Gather Study Set up requirements through discussion and communication with relevant stakeholders.
- Perform Database Set up and validation to ensure quality study design for data collection.
- Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
- Ensure that all the deliverables are of expected quality standards and meet customer expectations.
- Support Training of New joiners.
- Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
- Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL.
- Manage the development and implementation of new technology / database revisions.
- Work closely with the programming team for process innovation and automation.
- Be compliant to trainings and eSOP reading.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Sydney NSW, Australia