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Local Trial Manager

ICON Strategic Solutions - APAC
Start date
6 Jan 2023
Closing date
5 Feb 2023

View more

Clinical Research, Clinical Operations
Full Time
Contract Type
Experience Level
Experienced (non-manager)
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Job Details

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

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 Trial Manager" to work closely with our client, a leading pharmaceutical company.

To act as the Functional Lead from Clinical Operations with responsibility for delivery of all Clinical Operations aspects of clinical studies ensuring consistency with related SOPs, study contracts, timeline and budgets.

Key responsibilities

The responsibilities of the Project Manager Clinical include, but are not limited to:
• Assumes responsibility for an individual project, or many projects
• Communicates in an optimal way, making sure that specific client objectives are met
• Responsible for the set-up and maintenance of the project(s)
• Partially responsible for the development of research protocols and documents, such as CRF, publications and clinical reports
• Responsible for the management of the study budget
• Establish and manage the study time-lines and protocol specific SOPs
• Ensuring that the many different tasks during clinical development and marketing are achieved
• Selection of research sites
• Involves little to no people management and focuses completely on the product development programme and trials

• Interpersonal skills: open communication, coping and dealing with pressure
• Management skill: complicated decision making, dividing delegating, planning and organizing, coordinating, problem solving, mediator, result orientation

Required experience and qualifications

• Experience within the clinical trial management field, with some experience of taking a lead CRA role in the management of studies/trials. Five years experience within the clinical monitoring arena is preferred.
• Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
• Knowledge of project management processes and tools.
• Fluent in written and spoken English. Additional language skills desirable.
• Computer literate.
• Due to the nature of this position it may be required for the employee to travel.
• University/Bachelors Degree in medicine, science or equivalent degree/experience.

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know


ICON is the leading provider of Functional Service Provision (FSP) globally. Our team of operational, functional and therapeutic specialists offer a range of FSP models that can be customised to deliver the most efficient operating model for your organisation. We bring a suite of capabilities, expertise and technology to augment your operations, increase R&D efficiencies and improve site engagement to access patient populations and deliver timelines and milestones. We have deployed FSP solutions across all major functions from clinical monitoring and project management through data management, statistical programming and beyond. ICON FSP experience 90+​ FSP partnerships 13,000+​ Employees 90+​ Countries Functional areas Our offering includes a range of globally scalable FSP solutions that are customised to provide support where and when you need it. We have significant experience in providing bespoke FSP solutions, particularly in: Study start-up Project Management Clinical monitoring Pharmacovigilance / Safety Clinical Supplies Management Data management Biostatistics and programming Contracts management Investigator payments Clinical vendor management & category management Medical writing Medical affairs Regulatory affairs Regulatory publishing

Find Us
Central Square
Suite 1701
323 Castlereagh St
2000 Australia
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