Aktuelle Jobs im Zusammenhang mit Clinical Research Trials Coordinator - Melbourne - Buscojobs
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Clinical Trial Coordinator
vor 1 Woche
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Clinical Trial Coordinator
vor 1 Woche
Melbourne, Österreich Monash VollzeitAlfred Health Alfred Health is a leader in health care delivery, improvement, research and education.We are the main provider of health services to people living in the inner southeast suburbs of Melbourne, from ambulatory to inpatient and home and community-based services.Fixed Term – 12 month contract – possibility to extendFull time : 76 hours per...
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Clinical Trial Coordinator
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Melbourne, Österreich Buscojobs VollzeitJob DescriptionClinical Trials Coordinator Permanent full-time role with competitive remuneration and benefitsThe ideal candidate will be based in Sydney, AustraliaWork with a high-performing, agile, and passionate teamAs a Clinical Trial Coordinator (CTC), you will play a key role in providing administrative support to our company's Global Clinical Trial...
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Clinical Trial Coordinator
vor 2 Wochen
Melbourne, Österreich Monash VollzeitAlfred Health Alfred Health is a leader in health care delivery, improvement, research and education.We are the main provider of health services to people living in the inner southeast suburbs of Melbourne, from ambulatory to inpatient and home and community-based services.Fixed Term – 12 month contract – possibility to extend Full time : 76 hours per...
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Vor 4 Tagen
Melbourne, Österreich Monash VollzeitAlfred Health Alfred Health is a leader in health care delivery, improvement, research and education.We are the main provider of health services to people living in the inner southeast suburbs of Melbourne, from ambulatory to inpatient and home and community-based services.Fixed Term – 12 month contract – possibility to extend Full time : 76 hours per...
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Research Trial Coordinator
Vor 5 Tagen
Melbourne, Österreich The University Of Melbourne VollzeitJob no: 0063358Location: ParkvilleRole type: Full-time; Fixed-term for 24 monthsFaculty: Medicine, Dentistry and Health SciencesDepartment/School: Department of General Practice and Primary CareSalary: UOM 6 – $96,459 – $104,413 p.a.plus 17% superAbout the RoleThe Department of General Practice and Primary Care seeks a research trial coordinator in our...
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Research Trial Coordinator
Vor 7 Tagen
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Research Trial Coordinator
Vor 4 Tagen
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Clinical Trial Coordinator Registered Nurse
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Clinical Trial Coordinator Registered Nurse
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Haematology Clinical Trial Coordinator
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Melbourne, Österreich St Vincent's Health Australia VollzeitHaematology Clinical Trial Coordinator page is loadedHaematology Clinical Trial CoordinatorApply locations VIC - Melbourne, CBD & Inner SuburbsTime type: Full timePosted on: Posted TodayTime left to apply: End Date: January 3, 2025 (30 days left to apply)Job requisition id: JR139858Job Description:• Permanent, Full-time position (2 x positions) •...
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Clinical Research Associates
Vor 4 Tagen
Melbourne, Österreich George Clinical VollzeitClinical Research Associates - all levels - Australia-wide A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence 20+ years of experience, ~500 people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe Full range of clinical trial services to...
Clinical Research Trials Coordinator
vor 2 Monaten
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Northern Beaches Clinical Research Wollongong NSW This is a full-time & permanent opportunity for a Clinical Research Coordinator to join our team at our clinical research site in Wollongong.
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 the 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 within 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.
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