About Us:

UNIQ Trials is a full-service Contract Research Organization (CRO) dedicated to navigating the complexities of bringing new medical products to market. With a legacy of excellence that began 15 years ago we have grown from a small, passionate team into a global network of experts committed to delivering high-quality services in medical writing, clinical monitoring, project management, biostatistics, data management, safety and medical monitoring, and quality assurance. Our international team continues to deliver innovative clinical trial solutions across diverse therapeutic areas, ensuring the success of every study we manage.

The role:

We are looking for an experienced Project Manager who will b e responsible for managing clinical projects from commencement to completion and will be the interface between our clients and sites, managing multiple trials across many therapeutic areas at any one time ensuring the studies are delivered on time and within budget.  This role is perfect for someone who is driven and likes working in a fast-paced CRO.

Core 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.

To be successful in the role, we’re looking for candidates with:

• 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.

UNIQ Trials 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 UNIQ!