Current jobs related to Study Start Up Submissions Coordinator - Melbourne City Centre - HAYS

  • Study Start Up Submissions Coordinator

    2 weeks ago

    Melbourne, Australia Medpace, Inc. Full time

    Job Summary: We are currently seeking a full-time, office-based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you...

  • Country Approval Specialist

    7 days ago

    Melbourne, Australia PPD Full time

    PPD is recruiting for our growing Australian study start-up team. As one of the world's largest CRO's, our CRA's have the opportunity to work on challenging projects across a wide range of therapy areas with some of the most innovative pharmaceutical and biotech companies in the world PPD is proud to employ over 20,000 employees worldwide, across 47...

  • Study Start Up Associate Ii

    1 week ago

    Melbourne, Australia ICON Full time

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

  • Global Study Submissions Specialist

    4 days ago

    Melbourne, Victoria, Australia beBeeRegulatory Full time $100,000 - $115,000

    Global Study Submissions ManagerWe are seeking a highly skilled and experienced Global Study Submissions Manager to join our Clinical Operations team in Melbourne, Australia.Key Responsibilities:Manage and execute global study submissions efficiently;Perform quality checks on submission documents and site essential documents;Prepare and approve informed...

  • Study Start Up Associate Ii

    6 days ago

    Melbourne, Australia ICON Full time

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

  • Centralized Start-up Lead

    1 week ago

    Port Melbourne, Australia Labcorp Full time

    **The Opportunity** The Centralized Start-up Lead primarily oversees and manages the amendment phase of domestic and/or international clinical trials. Where required, may also take on start-up tasks under direction of the Start-up Lead. **Responsibilities (but not limited to)** - Develop an amendment submission and approval strategy in conjunction with the...

  • Submissions Coordinator

    7 days ago

    Melbourne, Australia Bloomfield Tremayne & P Full time

    **Major Infrastructure Projects** ***: - **Leading Studio with Stunning Views** ***: - **Work alongside the Director** Be a part of the next phase of Melbourne infrastructure. This fantastic mid-sized Studio has just seen an influx of top-tier infrastructure projects. With their pipeline of work over the next 2 years already secured, they are looking to...

  • Regulatory Submissions

    2 weeks ago

    Melbourne, Victoria, Australia Medpace Full time

    Regulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceRegulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceWe are currently seeking a full-time, office-based* Study Start Up Submissions Manager to join...

  • Regulatory Submissions

    2 weeks ago

    Melbourne, Victoria, Australia Medpace Full time

    Regulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceRegulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceWe are currently seeking a full-time, office-based* Study Start Up Submissions Manager to join...

  • Submissions Coordinator

    3 days ago

    Melbourne, Australia Icon Full time

    Help us continue to deliver outstanding projects! - Collaborative and supporting submissions team - Flexible working arrangements **Why Icon?** With a workforce of nearly 800 employees and with projects across Australia and New Zealand Icon is a large, diversified construction business, and supported by our parent company Kajima Corporation. With over 80...

Study Start Up Submissions Coordinator

2 weeks ago

Melbourne City Centre, Australia HAYS Full time

Study Start Up Submissions Coordinator role open to all levels of experience up to Principle Level.
**Your new company**
***
This global CRO is looking for an experienced Clinical Study Start
- Up Specialist to join their small office
- based team in Melbourne. This organisations is working with international pharmaceutical and biotech organisations to run their clinical trials globally.
They are renown for their great training and development program and offer a clear career path for their employees. As a Site Contracts and Budgets Specialist you will be joining an award winning CRO with an excellent reputation. Hays Life Sciences are currently supporting this company with a number of job opportunities in Australia.

**Your new role**
***
You will be involved in the negotiation of study contracts with investigators and study sites. You will be involved in ensuring the agreements are compliant with study protocols and the legal and regulatory requirements governing trial conduct. You will also be involved in the negotiation of study budgets with sites. You will cover the ANZ remit and countries within APAC may also fall within your portfolio. You will be looking after existing projects whilst also working on new trials setting up. This role is reporting to a manager based in Melbourne and you will be joining a global team. There is scope for career development and regional responsibilities into the future.

**What you'll need to succeed**
- Bachelor's degree or equivalent
- Previous working experience in similar role ideally at a sponsor company or CRO in Australia or New Zealand
- New Zealand and/ or Australian site knowledge advantageous
- Knowledge of regional and national regulatory guidelines and EC regulations
- Very good oral and written communication skills
- Self
- motivated, pro
- active, lateral thinker with excellent organisation skills
- Negotiation skills
- Attention to detail
- Full working rights in Australia

**What you'll get in return***
- Competitive salary
- Growing, international company
- Excellent corporate training
- Great team
- and company culture
- Work on cutting
- edge, orphan drug trials

**What you need to do now**

If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

**LHS 297508** #2694524