Clinical Programmer jobs in Florida

Who are we?

• A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence
• 20 years of experience, ~500 people managing 39 geographical locations throughout the Asia-Pacific region, USA, and Europe
• Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trial
• We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, cardiovascular and chronic diseases across various phases to improve the health of millions worldwide.

Why work with us?

• We are a global team making a difference in the world – our clinical trials improve the health of millions worldwide
• Competitive salary and benefits
• Flexible and agile working arrangements - onsite, hybrid or WFH (dependent on location)
• Strong and diverse Learning & Development opportunities including exposure to all aspects of clinical trials with an unparalleled network of Scientific Leaders to learn from
• A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities and other fun events!

What does the role involve?

The award of new projects has resulted in opportunities arising for well-experienced Clinical Research Associates to join us. We are open to all experienced CRA applicants across Australia.

You will be working on exciting new projects with regional and/or global teams in a CRO that truly has an impact on improving the health of millions worldwide. You would be able to:

• Prepare, organise, conduct and follow-up routine monitoring and close out visits as per relevant study plan
• Motivate and train investigators and site staff to ensure obligations in regards to study timelines
• Ensure ethics submissions are made by investigator sites in a timely manner
• Adherence to ICH-GCP and any other regulatory guidelines and requirements including adverse events and serious adverse event reporting
• Compliance with mandatory SOPs as agreed for the study
• Complete all reports accurately and within the predetermined timelines.

What are our expectations of candidates?

• Experience in a similar role within a CRO or Pharmaceutical company
• Excellent co-ordination and time management capabilities including the ability to prioritise demands
• Tertiary qualifications in Science or a relevant area preferred
• Strong interpersonal skills including the ability to communicate well with various types of people
• Excellent verbal and written communication skills
• Proficiency in the use of the Microsoft Office suite of products.

You must be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence alongside your colleagues globally - we keep each other in check and work better together!

How do I apply and what if I'm interested in a role in future or want to refer someone?

Apply via LinkedIn or send your CV, referral or confidential query to careers@georgeclinical.com and our friendly HR team across the world will reach out as appropriate soon. Please provide your full contact details, the location you are applying for, whether you are interested in a current or future opportunity and we'll be in touch. We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.

How do I learn more about the roles and George Clinical?

Follow us on Linkedin to see our regular updates and how we celebrate our people and success across our business and projects! You can also visit us at www.georgeclinical.com.

We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.

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