In-Demand Clinical data manager Jobs

Clinical Data Associate
Avance Clinical —Sydney NSW
- Contract
- Nursing
- Management
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Quick Apply
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Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
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Remote Clinical Coder/Health Information Manager
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First 2000 Days Clinical Coordinator
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Clinical Coder / Advanced Clinical Coder - Casual
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Clinical Coder
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PCI Pharma Services —Moorabbin VIC
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Clinical Trial Nurse - Casual
University of the Sunshine Coast —Morayfield QLD
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Peter MacCallum Cancer Centre —Parkville VIC
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Experienced CRCs & CRAs | Relocate to Brisbane and Advance Your Clinical Research Career
Thermo Fisher Scientific —Brisbane QLD
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SCRA I
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Supernova Medical Centre —Tarneit VIC
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National Clinical and Quality Data Manager
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Research Project Manager
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12d

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Clinical Data Associate

Avance Clinical
Sydney NSW

Quick Apply

Job Details

Contract

Qualifications

Nursing
Management
Research
Administrative experience
Bachelor's degree
Pharmacy
Clinical trials
Communication skills

Full Job Description

New opportunity to join the Clinical Data team on contract
Supportive managers
Global and stable CRO

If you are a life science graduate, with ICH GCP awareness, that has exceptional verbal & written communication skills and administration experience preferably from a clinical trial background we'd love to hear from you.

Who are we? We’re Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980’s. If you already work in this industry you’ll know that we are experts in our field.

Why should you join Avance Clinical? We appreciate that our most important asset is our people. We offer a fun, friendly work environment and a culture that values honesty and respect. We have a strong sense of team. We genuinely appreciate each individual but recognise the collective when achieving success. We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.

The role
The Clinical Data Associate I (CDA I) is responsible for supporting the Data Manager by drafting the relevant documents and cleaning the data on an ongoing basis as outlines in the SOP.

Core Responsibilities

Develop study-related documents or plans under the supervision of the Data Team Manager.
Preparation of Data Management Plans and assist with development of Edit Check Document with the support of a mentor.
Preparation of clean and erroneous dummy data.
Perform data review and cleaning of data collected during the trial and raise queries in the database while conducting cleaning activities for eCRF studies.
MedDRA / WHO-DD Coding with the support of a mentor and/or review of coding.
Liaise with a variety of different team members to ensure good communication across each study.
Archiving of studies, including EDC specific documentation.
Other duties as directed by Line Management or delegate in line with skills, experience and/or qualifications.

Departmental Responsibilities

Foster the on-going commitment to maintaining a healthy team culture and promoting good morale, by actively participating in regular Data Management Meeting.
Maintain effective communication with other members of the department.
Proactively identify risks related to departmental service provision and assist in their mitigation and resolution.
Participate in internal Quality Assurance activities as required, including responding to internal audit findings.
Organisational Responsibilities
Embrace the core values of Avance Clinical and endeavor to display those attributes at all times with clients and staff alike.
Commit to Avance Clinical training programs.
Adhere to Avance quality systems.

Qualifications, Skills and Experience

Bachelor’s level degree in life sciences, pharmacy, nursing or equivalent field (highly regarded), or appropriate industry experience.
Previous experience as a CDA in a Contract Research Organisation (CRO) or Pharma company for at least 1 year.
Awareness of ICH GCP Guidelines and other applicable regulatory requirements (desirable).
Clear understanding of the requirement to adhere strictly to client confidentiality.
Effective written and oral communications skills, including the ability to keep clients, senior management and other stakeholders informed of project updates and other pertinent information.
Demonstrated ability to take initiative in problem solving and in exercising good judgement.
An understanding of Privacy Legislation as it applies to the Clinical Trial Environment (desirable).
Ability to work independently or in a team environment as needed.
Willingness to work in, and be supportive of, a positive and dynamic team culture.

What we offer

Stimulating work
Project diversity
An intellectual challenge
An agile & flexible workplace
Opportunity to progress
Stability
Sense of community
A leadership team that are working together on a common goal
Flexible work options
Great tools / tech to do your job
A competitive salary & an extra days holiday for your birthday!

What next? As a growing business we’re looking for likeminded people to join us – we hope that’s you.

To join our team please submit your CV & cover letter as one Microsoft Word document
You must have full Australian working rights to be considered

Quick Apply

Refine Your Search

clinical data manager jobs

Clinical Data Associate

Clinical Coding Specialist

Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane

Clinical Trial Project Manager

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First 2000 Days Clinical Coordinator

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Clinical Manager

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Project Manager - Clinical

Clinical Trial Nurse - Casual

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Experienced CRCs & CRAs | Relocate to Brisbane and Advance Your Clinical Research Career

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SCRA I

Allied Health Manager

National Clinical and Quality Data Manager

HIM /Clinical Coder

Clinical Manager

Research Project Manager

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