Clinical Trial Manager

Employer
ICON Strategic Solutions - APAC
Location
Taiwan
Salary
Competitive
Start date
24 Jan 2023
Closing date
23 Feb 2023
You need to sign in or create an account to save a job.

Job Details

Regional Clinical Study Manager

Location: Australia, Singapore or Taiwan. (Home-based)

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.

Current Vacancy:

This is an exciting opportunity to join an embedded sponsor team as a Clinical Study Manager, home-based in Australia. The Clinical Study Manager will lead groundbreaking trials across a number of therapeutic areas in the region (including Immunology, Hepatology, Dermatology or Cardiovascular). You will be accountable for the end to end performance and project management for assigned protocls in the Asiapacific region in complaince ICH-GCP and with country specific regulations.

Key Responsibilities:
  • Act as main point of contact between Country Operations and Clinical Trial Lead.
  • Responsible for project management of the assigned studies: pro‐actively planning, driving, delivering and tracking execution and performance of deliverables/timelines/results to meet country commitments
  • Escalatesasneededdifferentchallengesandissues
  • Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies
  • Ensure effective study risk management
  • Collaborates internally with HQ functions and locally with PV, Regulatory and GMA to align on key decisions on studies


Requirements:
  • Tertiary degree in relevant field
  • Minimum 1 years experience in a clinical trial management role
  • Minimum 9-10 years clinical research industry experience
  • Previous site monitoring (at least 6 years) and CRA oversight experience
  • Global trial experience is mandatory
  • Excellent communication skills
  • Previous clinical trial experience across multiple countries in region preferable.


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.

Company

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
Website
Location
Central Square
Suite 1701
323 Castlereagh St
Haymarket
NSW
2000 Australia
Australia
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert