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Job details

Location
Melbourne
Salary
Negotiable
Job Type
Full Time
Ref
BBBH35911_1612398357
Contact
Jillian Swoyer
Posted
24 days ago

Job details

Location
Melbourne
Salary
Negotiable
Job Type
Full Time
Ref
BBBH35911_1612398357
Contact
Jillian Swoyer
Posted
24 days ago

About the Company

Our client is a full-service clinical contract research organisation (CRO), who cover phases I-IV across biotechnology, pharmaceutical and medical device industries. This company works within all major therapeutic areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. This company ranks amongst top CROs for site ratings across multiple areas including CRA training, preparation & organisation, accessibility of staff and open communication.

About the opportunity

Our client is currently seeking an experienced Clinical Trial Managers (CTM)/Clinical Project Manager to lead the clinical research studies for the Asia Pacific region. This is an opportunity to step into a role within an established Contract Research Organisation and bring your experience and knowledge from working within a similar role in a CRO or Pharmaceutical organisation. You will be working with a market leader in the oncology and rare diseases.

Responsibilities

As a CTM you will be responsible for conducting the full breadth of clinical trials from start up to close out. You will be the interface between the clients and trials sites and expected to work in accordance with applicable ICH-GCP guidelines and regulatory requirements. You will work across phases I-IV, within the oncology and rare diseases, amongst other therapeutic areas. CTMs are also accountable for guiding a cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, and medical monitoring staff.

Skills and Experience

  • At least two years of Clinical Project Management experience in Asia Pacific region ideally in a CRO environment

  • Understanding of clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines

  • Experience in servicing a broad range of therapeutic product stakeholders

  • Bachelor of Science or equivalent

  • Strong passion for monitoring

  • Solid communication skills, both written and verbal

Why this opportunity is right for you

  • Fantastic opportunity to work with a fast-growing CRO

  • Personalised fast training program based on your experience and therapeutic preference

  • Competitive travel bonus

  • Low staff turn over

  • Internal growth opportunities

  • Extremely supportive line managers and established career progression paths.

  • Bring your passion of monitoring to a global organisation

How to Apply

Click apply or contact Jill Manson, Recruitment Consultant on 0412 783 755 for a confidential discussion.

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