About Project Management

Our approach to managing studies is grounded in transparency and clear communications that unlock efficiency and position for success, during each and every stage of the project lifecycle. Fully compliant with International Guidelines and modern regulations, we work in an agile, collaborative, transparent, and efficient way, prioritising flexibility and inclusivity so that you can achieve your goals in the most time- and cost-effective way possible. From global registration studies to single-country post-marketing studies (and everything in between), each project receives a dedicated and experienced Project Manager who will track and report on progress, timelines and milestones to give you maximum transparency and peace of mind.

In more detail

Streamlined approval processes

Setting up for success from the start by charting Ethics Committee approvals and necessary regulatory notifications

Development and implementation

Putting together a winning patient recruitment strategy and world-class project monitoring through Phase I-IV studies

Education and certification

Taking an accessible approach to site personnel education programs and certification protocols

Contract Research Organisation (CRO)

Third-party vendor management

Helping you to deliver projects on time and on budget by managing all third-parties

Storing your data securely

We complete comprehensive and regular reviews of investigational product accountability and storage

Resolving queries quickly

Our clinical team and medical coders work to resolve data queries quickly and efficiently

Documentation and promotion

We can execute study mail outs and newsletters to keep key stakeholders informed

Inventory Management

Site closure and completion

Locking your database and securing the integrity of your data, followed by close out of sites

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