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Capabilities
Pioneers with Groundbreaking Capabilities
In the complicated word of clinical trials, we strive to make things easy using our decades of experience and size to our advantage — and yours. Experience faster starts, effective recruitment, a streamlined trial process and consistent delivery of high-quality data with exceptional participant care.
Accelerated Start Up
- Quick response to feasibilities 48hrs
- Fast ethics submission within 7 days
- Simplified ethics approval 4–6 weeks
- Established Māori Consultation Process in New Zealand
- Rapid site selection service
Our teams are experienced in delivering streamlined processes, including a 48hr response time to initial feasibilities and fast-tracked ethics approval of four to six weeks.
Reliable Recruitment
Patient recruitment remains the biggest challenge in clinical trials and Momentum is setting a world leading standard by leveraging years of experience in marketing and patient engagement strategies to meet this challenge.
Together, our centralised recruitment, marketing and participation experience teams ensure our database is in a continous cycle of growth and potential participants are kept engaged, enabling Momentum to deliver fast and reliable recruitment with very high retention levels for every study.
Attract: Our dedicated in-house recruitment team takes a proactive approach to database growth, using technology to drive a continual cycle of recruitment and segmentation. This always on strategy enables us to cultivate a large and diverse pool of potential participants who are ready to engage at a moment's notice and are available well before a study is even awarded.
Convert: Utilising a combination of technology as well as strategic partnerships in our local communities, we reduce barriers to participants joining a clinical trial to build a high-volume database that can deliver highly targeted participants for specific studies.
Retain: We combine broader marketing initiatives using specific softward, with localised grassroots efforts to highly targeted areas to nurture our continually growing database. We deploy a strategic and systematic approach to our communications with potential participants to keep our database warm and ready to register as soon as a relevant study is available.
Advocate: Between our centralised communications and our local clinical teams, we deliver an amazing service to our participants so they are highly motivated to fully participate in their study, they refer their networks to our studies and they participate in further studies.
Streamlined and Integrated Process
- A single contract and budget for multiple sites across the region
- Centralised functions for accelerated start up, recruitment and execution
- Seamless coordination and oversight of trials at multiple sites across the region
- Dedicated team for consistent communication and fast response
By partnering with Momentum, sponsors receive a dedicated central contact for consistent communication throughout the trial process, enabling partners to make timely decisions and provide regular stakeholder updates.
Our end-to-end support system allows for efficiency during the intricate clinical trial journey to ensure sponsors and participants experience consistent, first-class care.
A central point of contact for sponsors, plus a single contract and budget that covers all our sites across both countries ensures you’ll experience the most efficient trial management.
Experienced Researchers
- 20 years’ experience of proven delivery of high-quality data
- Led by experts with extensive sponsor and CRO experience
- Over 200 Phase Ib - IV clinical trials delivered
- Expertise and Infrastructure to conduct a diverse range of therapeutic trials.
- Dedicated to providing a highly ethical patient first environment
- World class facilities equipped with latest medical technology
Over the last two decades, Momentum’s key personnel have evolved into a team of the most experienced investigators and researchers across Australia and New Zealand. Our network of 14 sites bring an unparalleled diversity of research experience and therapeutic capabilities. We can facilitate individual trials to be conducted across multiple sites, resulting in a consistent trial outcome.
Highest Quality Data and Compliance
- Dedicated quality offficer ensures each trial complies with ICH GCP
- Internal Clinical Governance Committee
- Proven culture of continuous improvement
- RealTime CTMS software enables remote monitoring and faster response to queries.
Momentum allocates a dedicated quality oficer to all clinical trials, to ensure they comply with the International Council for Harmonisation (ICH) E6 Good Clinical Practice (GCP) and the collection of high quality and credible data. We take pride in upholding the highest clinical trial standards with our GCP trained teams and IATA certified staff.
Connect with us
If you are interested in exploring how Momentum can assist with your next clinical trial, then please reach out to us here.
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