In-Demand Research coordinator Jobs in Wollongong, Nsw

Clinical Research Coordinator
Canopy Clinical Research —Wollongong NSW
- $85,000 - $90,000 a year
- Full-time
- Administrative experience
- EMR systems
- In-person
Quick Apply
Policy Coordinator
Big Fat Smile Group LTD —Wollongong NSW
- Full-time
- Writing skills
- Research
- Analysis skills
- Employee assistance program
Quick Apply
Education Program Assistant
University of Wollongong —Wollongong NSW
- $85,682 - $96,898 a year
- Part-time
- University
- In-person
- Communication skills
11d
Data Coordinator - Emergency Department, Shoalhaven Memorial Hospital
Illawarra Shoalhaven Local Health District —Wollongong NSW
- $71,072.43 - $73,287.41 a year
- Full-time
- Employee assistance program
- Gym membership
6d
Graduate Research Intern Placement Administrator
University of Wollongong —Wollongong NSW
- $85,682 - $96,898 a year
- Part-time
- Administrative experience
- University
- Bachelor's degree
10d

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Clinical Research Coordinator

Canopy Clinical Research
Wollongong NSW

Quick Apply

Job Details

Permanent | Full-time
$85,000 - $90,000 a year

Qualifications

Administrative experience
EMR systems
Clinical trials
Communication skills

Full Job Description

This is a full-time & permanent opportunity for a Clinical Research Coordinator to join our growing team at our clinical research site in Brookvale on the beautiful Northern Beaches of Sydney.

As the Clinical Research Coordinator, you will have a thorough understanding of all trials being conducted at your site, particularly the protocols, investigator brochures, participant information and consent forms, timelines, and safety reporting requirements.

Your other main responsibilities will include:

Establish and organise study files, including regulatory binders, study specific source documentation and other materials as required.
Working closely with patient recruitment team to ensure recruitment targets and timelines are met.
Liaise directly with patients to ensure they are aware of all trial related requirements and ensure they attend all trial related appointments and assessments.
Ensure research studies are conducted in adherence to the requirements of the International Conference on Harmonisation (ICH) guideline for Good Clinical Practice (GCP), Therapeutic Goods Administration (TGA), National Health and Medical Research Council (NHMRC).
Be available to discuss any trial related queries with patients and liaise with investigators to ensure all questions and concerns are addressed.
Schedule protocol specific assessments and procedures ensuring Investigators are available during study visits to perform required tasks.
Review patient EMR for each completed visit to ensure all data has been collected, all procedures properly completed and documented.
Ensure that all Adverse Events and Serious Adverse Events are properly reported withing expected timelines.
Maintain all study related documentation and ensure data queries are completed in a timely manner.
Complete all study close out activities including archiving of all study records.
Ensure all discrepancies and deviations are properly addressed and documented
Prepare for and host initiation, monitoring and close out visits
Maintain open and regular communication with key stakeholders, in particular sponsor representatives.
Assisting with audit and inspection preparations.
Perform ad-hoc duties as delegated by your supervisor.
Make sure all study related logs are up to date.

The successful candidate will have the following skills/experience:

Minimum 3 years’ experience in a similar role
Demonstrated experience in a clinical environment; which includes conducting and coordinating pharma sponsored clinical trials
Excellent interpersonal, verbal and written communication skills
Proficiency in using CTMS and EDC systems
Strong administration skills are essential to the success of this position
Ability to work independently with a high-level of initiative but also work well within a team
Demonstrated understanding of clinical trials methodology and knowledge of Good Clinical Practice (ICH-GCP) requirements
Ability to work within a team environment of Nurses, Phlebotomists, Receptionists, Doctors and the Site Director
High level of attention to detail

About us:

Walski Clinical Research is a dedicated, multi-site, private Clinical Trials network on the East-coast of Australia. We conduct trials on a broad therapeutic range, from Phase 1 through to Phase 4. We excel in generalist studies with a large volunteer recruitment pool and have proven to be equally capable in delivering results for more specialist indications requiring patients.

If this opportunity interests you, please apply with your current CV

Job Types: Full-time, Permanent

Pay: $85,000.00 – $90,000.00 per year

Work Authorisation:

Australia (Required)

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in wollongong, nsw

Clinical Research Coordinator

Policy Coordinator

Education Program Assistant

Data Coordinator - Emergency Department, Shoalhaven Memorial Hospital

Graduate Research Intern Placement Administrator

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