Clinical Research Coordinator Specialist

6 days ago

Melbourne, Victoria, Australia beBeeClinical Full time

$95,223-$103,327* + generous salary packaging options

The laboratory has many independent functions and also links with major universities and research institutes in Australia and overseas.

As a Clinical Research Coordinator Specialist, you will work alongside a team of study coordinators and study physicians to conduct clinical trials according to trial protocols. You will collaborate with clinical teams for recruitment and with other centres undertaking the trials and contribute to the research and professional activities of the lab.

Please note: as part of the role some local, interstate and international travel may be required to conduct clinical trials and to attend meetings related to clinical trials.

Key Responsibilities:

- Organise and co-ordinate ongoing clinical research studies including completion of case report forms, standard operation procedures, participant care and physician involvement.
- Maintain and develop own knowledge and skills in areas of research through appropriate journals and other literature, as well as trial-specific training.
- Identify and recruit potential study participants and screen them for suitability for study trials as per eligibility criteria.
- Carry out all relevant study-related tasks, ensuring adherence to protocol and good clinical research practice.
- Perform venepuncture, and deal with handling, processing and storage of blood and urine specimens. This includes maintaining awareness of appropriate blood handling procedures in relation to safety and laboratory techniques.
- Perform study visits on participants as required by the protocol and maintain accurate source documents.

Skills and Qualifications:

You will have:

- Strong experience and ability in coordinating clinical research studies. Previous experience in the field of diabetes clinical trials will be highly regarded.
- Excellent planning, coordination and organisational skills, including the ability to manage a range of tasks with conflicting priorities.
- A high level of interpersonal skills with a caring attitude towards study participants.
- Research experience including awareness of ICH-GCP Guidelines and relevant regulatory/statutory guidelines.
- Demonstrated ability to meet deadlines without compromising close attention to detail and accuracy.
- Excellent oral and written communication skills.
- Self-motivated with the ability to exercise initiative and to participate positively in a team environment.
- Demonstrated ability to maintain confidentiality of participant records.
- Previous experience in venepuncture, sample handling and processing, ECG measurement experience and intravenous cannulation skills.
- Excellent attention to detail with a high level of accuracy in data measurement and recording.
- Previous study recruitment experience.

Benefits:

Working at the Institute offers flexibility, professional development, and the opportunity to contribute to a centre of world renown. Benefits include an employee assistance program, as well as modern offices and laboratories adjacent to the Alfred Hospital and walking distance to St Kilda Road, Chapel Street, and Fawkner Park.

How to Apply:

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