Job Description

Job Header

Senior Clinical Research Associates / CRA and SCRA (multiple positions)

Advertiser: Avance Clinical Pty LtdMore jobs from this company

Job Information

Job Listing Date
13 Feb 2020
Location
Adelaide
Work Type
Full Time
Classification
Healthcare & Medical, Clinical/Medical Research

Senior Clinical Research Associates / CRA and SCRA (multiple positions)

Avance Clinical - our most important asset is our people. We offer a work environment and a culture that values honesty and respects its people.

Avance Clinical is a Contract Research Organisation which offers specialised services supporting clinical drug development for the pharmaceutical and biotechnology industry. 

Opportunity

If you are an experienced Senior Clinical Research Associate (SCRA) or Clinical Research Associates (CRA), are passionate about clinical research and want to work in a challenging and stimulating environment where what you do matters, then we want to hear from you now. 

This is a permanent position, we are open to it being either part time (0.8) or full-time and either home based from anywhere in Australia or home / office based if you are located in Adelaide.

As we continue to grow, we want our people to grow with our organisation. We offer training and career development opportunities to build the skills and progress the careers of our employees.

    Responsibilities

    Acting as the primary link between sites and sponsor, you'll be responsible for:

    • Performing start-up, initiation, monitoring and close-out visits along with maintaining appropriate documentation
    • Developing your skills and knowledge on clinical trials within a wide scope of therapeutic areas
    • Monitoring all aspects of studies to ensure compliance with GCP, study protocol and regulatory requirements and prepare monitoring reports
    • Development and review study protocols and other study related documents
    • Preparing ethics submissions and assist in preparation of Clinical Study Reports.

    Requirements

    Prior experience monitoring clinical trials, ideally within Australia and/or New Zealand. It is essential that you have a degree in science or other healthcare related discipline, between 4 to 5 years experience working as a SCRA / CRA in the pharmaceutical or CRO industry. You will need solid knowledge of Australian and New Zealand drug development process, clinical trial monitoring procedures, GCP guidelines and medical terminology is essential. On top of this you will need to able to show initiative and work well autonomously, within minimal supervision. 

    Benefits

    • Reputable growing CRO with stability
    • challenging and stimulating environment where what you do matters
    • a diverse and inclusive culture with a strong emphasis on team collaboration
    • training and career development opportunities
    • attractive remuneration

    To apply

    • To apply for this role please click on the 'APPLY' link and submit your CV along with a cover letter outlining your skills and experience - please submit as one PDF document.
    • As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process.
    • You must also have full Australian working rights to be considered.  

    www.avancecro.com.

    Avance Clinical - our most important asset is our people. We offer a work environment and a culture that values honesty and respects its people.

    Avance Clinical is a Contract Research Organisation which offers specialised services supporting clinical drug development for the pharmaceutical and biotechnology industry. 

    Opportunity

    If you are an experienced Senior Clinical Research Associate (SCRA) or Clinical Research Associates (CRA), are passionate about clinical research and want to work in a challenging and stimulating environment where what you do matters, then we want to hear from you now. 

    This is a permanent position, we are open to it being either part time (0.8) or full-time and either home based from anywhere in Australia or home / office based if you are located in Adelaide.

    As we continue to grow, we want our people to grow with our organisation. We offer training and career development opportunities to build the skills and progress the careers of our employees.

      Responsibilities

      Acting as the primary link between sites and sponsor, you'll be responsible for:

      • Performing start-up, initiation, monitoring and close-out visits along with maintaining appropriate documentation
      • Developing your skills and knowledge on clinical trials within a wide scope of therapeutic areas
      • Monitoring all aspects of studies to ensure compliance with GCP, study protocol and regulatory requirements and prepare monitoring reports
      • Development and review study protocols and other study related documents
      • Preparing ethics submissions and assist in preparation of Clinical Study Reports.

      Requirements

      Prior experience monitoring clinical trials, ideally within Australia and/or New Zealand. It is essential that you have a degree in science or other healthcare related discipline, between 4 to 5 years experience working as a SCRA / CRA in the pharmaceutical or CRO industry. You will need solid knowledge of Australian and New Zealand drug development process, clinical trial monitoring procedures, GCP guidelines and medical terminology is essential. On top of this you will need to able to show initiative and work well autonomously, within minimal supervision. 

      Benefits

      • Reputable growing CRO with stability
      • challenging and stimulating environment where what you do matters
      • a diverse and inclusive culture with a strong emphasis on team collaboration
      • training and career development opportunities
      • attractive remuneration

      To apply

      • To apply for this role please click on the 'APPLY' link and submit your CV along with a cover letter outlining your skills and experience - please submit as one PDF document.
      • As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process.
      • You must also have full Australian working rights to be considered.  

      www.avancecro.com.

      The application form will include these questions:
      • Which of the following statements best describes your right to work in Australia?
      • How many years' experience do you have as a clinical research associate (CRA)?
      • What's your expected annual base salary?
      • How much notice are you required to give your current employer?

      Report this job advert

      Be careful- Don’t provide your bank or credit card details when applying for jobs. If you see something suspicious .

      Share this role