Project Manager Early Phase Clinical Trials

Novotech; Melbourne; Remote; AUD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible working options

Paid parental leave

Wellness programs

Ongoing development programs

Job summary

A leading clinical research organization is seeking a Project Manager - Early Phase responsible for managing early phase projects and acting as the main contact for clients. Ideal candidates will have over 5 years' experience in clinical research, strong project management skills, and a relevant degree in life sciences. The company offers flexible working conditions, parental leave, wellness programs, and an inclusive work environment. Join the team to support innovative clinical research.

Qualifications

• Minimum 5 years of experience in early phase clinical research.
• Experience as an Associate Project Manager or equivalent is required.
• CRO experience is advantageous.

Responsibilities

• Determine project feasibility and assist Business Development.
• Provide guidance on scope of work and quality of deliverables.
• Manage operational project plans and timelines.
• Coordinate cross-functional project teams.

Skills

Project management

Clinical research

Stakeholder communication

Education

Graduate in clinical or life sciences

Job description

About the Role

The Project Manager - Early Phase is primarily responsible for the planning and management of all contracted responsibilities for assigned early phase projects and to act as the primary contact between Novotech and its clients.

Based anywhere in AU

Responsibilities

• Determine project feasibility, considering the needs of the sponsor as required to assist Business Development.
• Actively provide guidance and review scope of work, responsibilities, timelines and quality of deliverables.
• Understand the requirements of the Project Agreement and ensure Novotech performs these services to the required standards. Understand the inherent risks of the project and collaborate with management to ensure appropriate contingencies are initiated.
• Ensure set up and maintenance of operational project plans, timelines & study tracking tools (such as CTMS), and eTMF, as required.
• Work with the Vendor Manager to assess, appoint and manage study vendors to ensure the study is adequately supported, e.g. central laboratory, drug distributors, IRT providers.
• Coordinates workstream and cross functional project teams, such as Clinical, Regulatory, Medical, Biometrics and Pharmacovigilance.

Experience and Qualifications

• At least 5 years' experience within early phase clinical research studies and previous project management experience, including Associate Project Manager or equivalent
• Graduate in a clinical or life sciences related field.
• Relevant experience/qualifications in allied professions may also be considered.
• CRO experience is advantageous.

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to talking to you about working at Novotech.