Senior Clinical Research Associate - open to all EA locations

An opportunity has arisen for an experienced, adaptable and committed Senior Clinical Research Associate (SCRA) to join our dynamic team in any of the following locations - Hong Kong, Taiwan, Malaysia and South Korea.

We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.

We are searching for individuals who are organized, results oriented and able to handle changing priorities. Your willingness to extend yourself and take on new challenges with a 'can do' attitude.

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 or hybrid (depending 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!

About the Role

• Coordinate the identification, feasibility assessment and selection of investigators and sites to undertake the study
• Prepare, plan, organize and conduct pre-study (site selection) visits and report on these visits to assist in site selection
• Prepare and submit of regulatory and Ethics Committee packages and updates as appropriate in the local setting
• Negotiate site budgets, co-ordinate for site contract execution & site payments, and track site payments
• Develop and maintain appropriate monitoring tools and project specific documents
• Motivate and train investigators and ensure that the study site personnel have a good understanding of the protocol, the investigational product and the requirements of the study and that they can fulfil their obligations to conduct the study accurately and to deadlines
• Mentor, coach, and train junior staff members as directed by line management

What are our expectations of candidates?

• Tertiary qualifications in a related science or health care discipline
• At least 5 years experience in clinical trial monitoring within an academic, CRO or pharmaceutical environment
• Understanding of medical terminology and physiology
• Excellent interpersonal skills, presentation skills and the ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders
• Excellent organizational skills – ability to organize, take initiative and follow up independently
• Technological proficiency including Microsoft Office packages, electronic data capture and project management systems
• Ability and willingness to travel (up to 50%)

You will be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence.

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 [email protected] 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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