In-Demand Research assistant Jobs in Bedford Park, Sa

Clinical Trial Assistant
Avance Clinical —Greater Adelaide SA
- Contract
- Nursing
- Management
- Office
Quick Apply
6d
Research Associate in Hydrogeology / Hydrology
Flinders University —Bedford Park SA
- $90,930 - $110,197 a year
- Full-time
- Doctoral degree
- Data analysis skills
- Research
4h
Research Assistant, Rheumatology RAH
SA Health —Adelaide SA
- $66,442 - $69,504 a year
- Part-time
- Computer skills
- Communication skills
- Annual leave
- Employee assistance program
6d
Field Research Associate - Adelaide
Domain Group —Greater Adelaide SA
- Microsoft Office
- Education
- Bachelor's degree
Senior Clinical Research Associate I (FSP)
Thermo Fisher Scientific —Greater Adelaide SA
- Full-time
- Laboratory
- Patient monitoring
- Microsoft Office
- Parental leave
- Employee assistance program
Field Research Associate - Adelaide
CoStar Group —Greater Adelaide SA
- Full-time
- Microsoft Office
- Education
- Bachelor's degree
Registered Nurse - Access Assistants Program
SA Health —Adelaide SA
- $77,824 - $106,187 a year
- Nursing
- Commuter assistance
- Employee assistance program
Memory Trials - Clinical Nurse
SA Health —Greater Adelaide SA
- $90,913 - $114,917 a year
- Part-time
- Rehabilitation centre
- Acute care experience
- Leadership

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Casual Professional Register - Technical Support / Research
Flinders University —Bedford Park SA
Pursuant to Child Safety (Prohibited Persons) Act 2016 (SA) this position may be deemed prescribed.
Clinical Trial Assistant
Avance Clinical —Greater Adelaide SA
Bachelor’s level degree in life sciences, pharmacy, nursing or equivalent field (highly regarded), or appropriate industry experience.
Quick Apply
6d

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research assistant jobs near bedford park, sa

Clinical Trial Assistant

Avance Clinical
Greater Adelaide SA

Quick Apply

Job Details

Contract
6 days ago

Qualifications

Nursing
Management
Bachelor's degree
Pharmacy
Clinical trials

Full Job Description

Short term contract (6 Months), office-based positions at our office in Sydney/Adelaide/Melbourne

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?
At Avance we know 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’re seeking people that thrive in a positive environment, who are inquisitive and keen to have a genuine opportunity to learn and grow in a business that is expanding.

The role
The Clinical Trial Associate is responsible for supporting the Clinical Operations Team in an administrative capacity ensuring the trial is conducted in accordance with the protocol, company Standard Operating Procedures (SOPs), ICH GCP guidelines and other applicable regulatory requirements.

Please note – this role is office based 5 days per week.

Core Responsibilities

Support all aspects of clinical operations from study inception to completion, including:
- Organise, facilitate and take minutes for project/study team and functional group meetings.
- Establish, maintain and track completeness of Trial Master Files.
- Prepare Investigator Site Files and establish study documentation for assigned studies as required. o Liaise with study team members to ensure good communication across each study.
- Prepare and collect site documentation in conjunction with Project Manager and Clinical Research Associate, from study start up through to end of study.
- Manage receipt and shipping of study documentation to Investigator sites, maintain internal trackers.
- Maintain internal databases and assist the Clinical Operations team in ad hoc duties.
Participate in study-specific or vendor audits conducted by sponsors or regulatory agencies, and respond to audit observations, as required.
Ensure Serious Adverse Events are reported (initial and follow-up) as per protocol requirements.

Qualifications, Skills and Experience

Bachelor’s level degree in life sciences, pharmacy, nursing or equivalent field (highly regarded), or appropriate industry experience.
Previous exposure to a Clinical Trials environment (desirable).
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 judgment.
An understanding of Privacy Legislation as it applies to the Clinical Trial Environment (desirable).

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 working rights in Australia to be considered

At Avance difference is encouraged, its celebrated and it's something we strive for. We empower cultural, disability, LGBTI+, and gender equality.

Quick Apply

Refine Your Search

research assistant jobs in bedford park, sa

Clinical Trial Assistant

Research Associate in Hydrogeology / Hydrology

Research Assistant, Rheumatology RAH

Field Research Associate - Adelaide

Senior Clinical Research Associate I (FSP)

Field Research Associate - Adelaide

Registered Nurse - Access Assistants Program

Memory Trials - Clinical Nurse

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