Clinical Trials Operations Director

3 days ago

Sydney, New South Wales, Australia beBeeProject Full time $120,000 - $140,000
Clinical Trials Project Manager Role

We are seeking an experienced and skilled Clinical Trials Project Manager to lead our clinical trials from phase 1-4. The successful candidate will be responsible for managing the planning, implementation, ongoing evaluation, prioritization, reporting, and timely delivery of all operational aspects of allocated projects.

The ideal candidate will have a minimum undergraduate degree in Life Sciences, with a minimum of 3-4 years' experience in clinical research project management in CRO, Pharmaceutical, and/or Biotechnology. Formal project management certification is desirable. The candidate should have a proven track record of successfully leading clinical trials, with experience leading all functional capabilities involved in CRO-directed clinical research.

This role involves working closely with sponsor study teams, ensuring clinical research projects are properly resourced, managed, executed, and reported within established timelines and quality standards. The candidate will also be responsible for managing vendor relationships, coordinating activities, and participating in Investigator Meetings as required.

The Clinical Trials Project Manager will work collaboratively with our team to ensure the smooth execution of clinical trials, while maintaining effective professional relationships with sponsors, external customers, investigators, vendors, and internal project teams.

Key Responsibilities:
- Project manage assigned activities related to the management of multinational and local clinical trials from phase 1-4 and clinical registries.
- Manage the planning, implementation, ongoing evaluation, prioritization, reporting, and timely delivery of all operational aspects of allocated projects.
- Act as the point of contact for assigned projects for sponsor and internal study teams.
- Ensure clinical research projects are properly resourced, managed, executed, and reported within established timelines and quality standards.

Required Skills and Qualifications:
- Minimum Undergraduate degree in Life Sciences.
- Minimum of 3-4 years' experience in clinical research project management in CRO, Pharmaceutical, and/or Biotechnology.
- Formal project management certification desirable.
- Proven track record of having successfully led clinical trials, with experience leading all functional capabilities involved in CRO-directed clinical research.

Benefits:
- Engaging work environment that promotes collaboration within the multi-disciplinary team.
- Internal career development opportunities nationally.
- Working with a vibrant team aligned with providing the best patient experience possible and outcomes.
- Access to confidential support for employees and their family members.

About Us:
We aim to build a culture of care that is patient focused and performance driven. We are always improving, designing new and higher standards for clinical excellence and patient satisfaction.

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