Our services
We’re not a run-of-the-mill recruitment firm. Why? Because we live and
breathe clinical operations and development. It’s who we are.
How can we Help Your Project?
Our consultants can enrich your research programme at multiple points of the study lifecycle. There is no prescribed methodology: we pride ourselves on delivering a wide array of main and niche services, meaning you only pay for what you need.
We strive to deliver a solution for your specific requirements – no task is too small or too big. Thanks to the unique Momentum-Pharma model, our services are always relevant to the skills you’re seeking. No cross-charging or unnecessary overheads for services that aren’t of use.
Main Services
We provide a variety of traditional outsourced services to meet your needs. These are designed to build a solid foundation for your study, ensuring you have a smooth path to success.
Niche Services
Over the years, we have fulfilled even the most unique and complex roles with best-fit consultants. If you require specialist services that aren’t listed on our site, just let us know. We love a challenge.
Main services
Quality control visits >
Our Quality Control Monitors provide essential CRO oversight, assessing the proficiency of the CRO monitor to conduct assigned tasks and adherence to the Clinical Monitoring Plan. They also report on the compliance of the site according to ICH-GCP, inclusion exclusion criteria, safety monitoring and risk assessment.
Project Management >
Our experienced project managers can initiate, plan, execute, control and close a study in line with your goals and specific success criteria. We have a global focus, allowing us to deliver project managers for both US-based and international clinical trials.
Senior level CRAs >
Experts in their local territory and regulations, our senior-level CRAs can give you unrivalled insights into key regions. Each has an average of 15 years’ experience; many are multi-lingual and can monitor across different countries.
Medical monitor >
Our experienced pharmaceutical physicians uphold the highest standards of medical support, interim management and emergency intervention. They are experienced in medical affairs and clinical development, with a wide array of disease indications.
Regulatory services >
We can perform your National Competent Authority and Ethics submissions and support all regulatory services throughout the lifecycle of your study. Our experts can guide you on New Clinical Trials Regulations and the EU Voluntary Harmonisation Procedure.
Inspection Readiness >
We take the stress out of auditing, with resources to conduct GCP Investigator Site audits (Phase I–IV), Vendor Qualification and In-process audits, Internal Process, GMP and GLP audits, and Gap Analysis. We can also support GCP and Site Management training, Mock Inspections, Inspection Preparation, Assists at Inspections and advice on inspection responses.
Rescue teams >
If an issue occurs, we can jump in and support you with a co-monitoring service. We can help you quickly identify experienced consultants who can steer you through a busy or rough period for a short term or even longer duration, if needed.
Medical Writing >
Our medical writers focus on Study Protocols, Patient Information Leaflets, Clinical Study Reports, Manuscripts, Product Monographs, Paediatric Investigational Plans, Risk Management Plans, Press Releases and Clinical Summaries, to name a few.
Supplementary main services >
We fill all types of unique roles for our clients, from report reviews and quality management to site feasibility and study activation roles.
Niche services
In addition to our main services, we have developed a unique suite of niche
provisions for our Sponsors. Our ability to cater to the most specialist
requirements is down to our 100% outsourced model. This ensures our clients
work with the best people for the role, at the most economic cost.
Oncology recist training >
Our consultant has spent over 20 years conducting Oncology clinical research studies and training groups. For solid tumour studies, our expert makes a real difference, outlining RECIST rules and ensuring CRAs are well equipped for reporting target vs non-target lesions. By providing clear explanations, tools and case examples, they work towards explicit, coherent response definitions.
Paediatric specialty focus >
For clinical trials that are uniquely relevant to the ethical and operational challenges of working with children, our consultants offer valuable support. From medical writing for children and their caregivers, to artwork for Assent and Informed Consent Forms, to expert advice for planning, writing and managing a paediatric study protocol, our experts can help.
Database design >
Our Director of Technology can take unwieldy sets of data and design them into user-friendly, validated, normalised groupings. These listings can be used going forward for communication plans, feasibility planning, patient identification and mapping. He can make sense of mountains of important data and turn it into something meaningful.
The Momentum Pharma Difference
At Momentum-Pharma our philosophy is simple: We listen. We strategise. We resource. Our vision is to accelerate
the development of new medicines by providing optimal teams and a solid foundation for a successful study. This
is what we believe in: our world class Affiliates and their ability to make a difference.
Unparalleled Consultants
We understand our client base because we’ve been them.
Teams all over the world
Our therapeutic area expertise is both deep and diverse.
Our cost efficient model
Our clients are allocated with the most adept, efficient resources.
Flexible and fast responses
We’re better able to focus on a tactical “plan of action”.
Ongoing dialogue
Our therapeutic area expertise is both deep and diverse.
Contact us
We love to listen, and we’re always happy to answer any questions. Contact us
via the form below and we’ll get back to you as soon as possible. Alternatively, visit our contact page.
