Services
Vendor management and oversight
- Argos Clinical helps clients identify and manage qualified vendors to help with their clinical study needs, and within the clients and their partners specific tender needs.
- We can assist and advise clients with proposals and selection of vendors such as across-the-board CROs, central and specialized labs, specialized equipment etc. Once the study is under way, we can help the sponsor manage the vendors to ensure key project milestones are met.
- Set -up and/or review of specific study plans for example project plan, monitoring plan, communication plan, safety monitoring plan
- SOP review and system UAT
Clinical project management services
- Planning and tracking of timelines
- Budgeting
- Meeting organisation and facilitation
- Set-up and/or review of vendor specific study plans
Clinical trial management services
- study document review and eTMF filing, eTMF review
- site approval, site activation, IP release
- administrative assistance with regulatory submissions
- site visit report review
- recruitment rate analysis and booster
Medical & scientific writing
We can help prepare abstracts, manuscripts, white papers or provide assistance with protocol development and informed consent forms
Independent committee management
We can help ensure adequate safety oversight and increase the reliability of your trial data by managing independent scientific committees
- charter development
- member selection
- contract development and negotiation
- clinical document retrieval
- identification of events
- planning and coordination of meetings
- post-meeting review and minutes
- communication of meeting results
- assuring blinding where needed
Liaison management
management of relationships with third-party stakeholders such as consortia, patient groups, funding agencies on behalf of a sponsor
