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Senior Clinical Research Associate

Job Title: Senior Clinical Research Associate
Contract Type: Permanent
Location: Sydney, Australia
Industry:
Salary: $90000 - $120000 per annum
Start Date: 2018-05-14
Reference: 61949
Contact Name: Dean Coleman
Contact Email: dean.coleman@nesgt.com
Job Published: April 27, 2018 00:45

Job Description

Clinical Research Associate / Senior Clinical Research Associate -  Sydney or Melbourne


Short Description:
Global CRO with a smaller more boutique start up feel, currently looking for either a Clinical Research Associate or a Senior Clinical Research Associate to join the team in Sydney or Melbounre. Working across a number of therapy areas and phases, this company looks for forward thinking and mature minded candidates who enjoy the flexibility that comes with it.

Key Benefits:
  • Home based Sydney or Home / office based Melbourne
  • Valued staff  with excellent training on offer and a clear path to promotions from within
  • Collaborative culture which allows for flexible working
  • Reduced Travel (up to 50% Negotiable)
  • Excellent package Benefits including generous salary, leave loading, flexible working and excellent progression opportunities
Company Profile:

Our client is a Global CRO who offers a much more Boutique feel than the usual “Big 5”. This role would be perfect for somebody looking to get out of a huge CRO/Pharma and be more valued as an individual within the business. They are looking for CRA ‘s to Senior CRA’s across a number of therapeutic areas to be office based in Sydney or Melbourne .  This is a well-established company however with a more unique and individual feel.

Responsibilities:

As a Clinical Research Associate / SCRA you will be the link between investigational site and sponsor to ensure the clinical trials are delivered to the appropriate timelines and resources.
  • Liaise between sites and different sponsors
  • Follow a relevant study plan and organise, prepare, conduct and follow up routine monitoring and closing out of visits.
  • Motivating and training investigators and site staff to ensure that obligations are met and in line with study timelines.
  • Adhere to ICH - GCP and any other regulatory guidelines and requirements including adverse events and serious adverse event reporting.
Requirements/You: 
  • You will be degree qualified with a Bachelors or higher degree in a health/science related field
  • You will have 2+ Years for CRA, 5 + Years SCRA independent monitoring experience within ANZ
  • Working knowledge of ICH-GCP Guidelines
  • Mature Minded /Self Sufficient / Forward Thinking
  • Strong Verbal and written communication and Interpersonal skills
  • Excellent organisational skills – ability to organise, take initiative and follow-up independently
What is the best way to secure this role? Apply for this job online via the link or send your resume directly to Dean Coleman by emailing dean.coleman @ nesglobaltalent.com . Confidential enquiries can be made by calling Dean on 02 9696 8016. Only shortlisted candidates will be contacted and we thank you in advance for your interest.