Ref #: 27569

Employment type: Permanent - Full-Time

Location: Australia

Posted: 11-Mar-2021


If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are hiring a Clinical Research Associate I to work closely with our client, a leading pharmaceutical company.


The key duties of the Clinical Trial Manager is to lead and manage clinical trials from start-up to close out across AUS and NZ in accordance with local regulations. You will be required to actively coordinate with global /regional trial managers whilst leading a team of CRAs and CTAs to ensure the country level study delivery is aligned with the global study project plan

Key Responsibilities:

• Leads and coordinates local trial team activities in compliance with relevant SOPs and regulations.
• Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.
• Acts as a local expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities.
• Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships
DOCS will be responsible for your career development and this is an area we take very seriously. Ask yourself this question. What if you are working in a pharma company / CRO and you don’t have the opportunity to gain that promotion you’ve been working towards because there isn’t the business need?
This won’t happen as we work with multiple global pharmas, biotech’s and medical device companies. That means, when there is inevitably a promotion opportunity, you will be first in line.

Required experience and qualifications
• Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry.
• Scientific background
• Proficiency with medical terminology
• Working knowledge of Local Regulations
• A demonstrated working knowledge of ICH/GCP Guidelines
• Excellent record-keeping skills and attention to detail