In-Demand Clinical supervisor Jobs

Clinical Research Coordinator
Canopy Clinical Research —Wollongong NSW
- $85,000 - $90,000 a year
- Full-time
- Administrative experience
- EMR systems
- In-person
Quick Apply
Clinical Supervisor - Behaviour Support Practitioner - Albury
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Registered Nurse – Clinical Supervisor (Urinary Care / Catheter Management)
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14d
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KB7 CARE —Mambourin VIC
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Clinical Supervisor (Acacia)
Serco Plc —Wooroloo WA
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Therapy Supervisor (BCBA) - Full-Time | Northern Beaches Sydney
Lizard —Sydney NSW
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NurseLink Healthcare —Bendigo VIC
- $50 - $80 an hour
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Program Supervisor/Family Support Worker
Bright Eyes Blue Mountains —Katoomba NSW
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Clinical Psychologist, Supervisor
Flinders University —Bedford Park SA
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Clinical Supervisor
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Registered Psychologist/Clinical Psychologist
thoughts and things —Ashfield NSW
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Security Officer
Certis Group —Geelong VIC
- Rotating roster
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Food Service Supervisor
West Gippsland Healthcare Group —Baw Baw VIC
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Senior Medical Officer
Galambila Aboriginal Corporation —Coffs Harbour NSW
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Senior Clinical Trial Manager - FSP (Tagalog proficient)
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After Hours Supervisor
Prestige Inhome Care —Remote
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Sterilisation Technician Supervisor
Hunter New England Local Health District —Tamworth NSW
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Clinical Research Fellow or Senior Clinical Research Fellow
University of Melbourne —Parkville VIC
- $124,656 - $176,065 a year
- Full-time
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8d

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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

clinical supervisor jobs

Clinical Research Coordinator

Clinical Supervisor - Behaviour Support Practitioner - Albury

Registered Nurse – Clinical Supervisor (Urinary Care / Catheter Management)

Surgical Resident Medical Officer - SALHN

Allied Health Professionals

Clinical Supervisor (Acacia)

AHS Supervisor

Therapy Supervisor (BCBA) - Full-Time | Northern Beaches Sydney

Chef- Aged Care

Program Supervisor/Family Support Worker

Clinical Psychologist, Supervisor

Clinical Supervisor

Registered Psychologist/Clinical Psychologist

Security Officer

Food Service Supervisor

Senior Medical Officer

Senior Clinical Trial Manager - FSP (Tagalog proficient)

After Hours Supervisor

Sterilisation Technician Supervisor

Clinical Research Fellow or Senior Clinical Research Fellow

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