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Clinical Trial Manager - Sponsor Office-based In Melbourne

Syneos Health - Australia - Australia,

Health, Medical & Pharmaceutical
Source: uWorkin


Working with a leading Global pharmaceutical company (Clinical Project Manager)
Why Syneos Health? Join a game-changing global company that is reinventing the way therapies are developed and commercialized. With More than more than 24,000 employees worldwide we bring clinical and commercial minds together to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.

Project Manager or Snr Project Manager
Permanent Full-Time
Melbourne office-based at Pharma
Great company culture - certified Great Place To Work in Australia
Be part of a supportive and collaborative team within the FSP model
Competitive package and working with innovative CRO


Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP's, and regulatory requirements.
Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer's and the Company's contractual agreement
Lead project team to ensure quality, timelines and budget management
Oversight for development and implementation of project plans
Plan, coordinate and present at internal and external meetings
Prepare project management reports for clients and management

Previous experience as a Project Manager working in clinical research or related relevant pharmaceutical industry experience
Bachelor's Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements
Strong organizational skills
Strong ability to manage time and work independently
Direct therapeutic area expertise within Oncology is highly preferable
Ability to embrace new technologies.
Excellent communication, presentation, interpersonal skills, both written and spoken