Research Partnership Opportunity

Request for Research Proposal:
We are calling on researchers, sponsors, academic institutions, and clinical partners to submit study concepts.

PURPOSE

UCTSS invites proposals for clinical studies aligned with our strategic focus on clinical research and healthcare product development. Selected applicants will be invited to partner with UCTSS on joint grant applications, feasibility assessment, study execution, and related research support.This call identifies strong research concepts with clear potential for partnership, external grant competitiveness, and meaningful impact.

Who can Apply?

  • Universities (Including undergraduate, MSC & PhD)

  • Hospitals & health systems

  • Research institutes

  • Biotech & pharma companies

  • Nonprofit organisations

  • Multidisciplinary research teams

Partner With Us And Get Access To:

  • Study feasibility review

  • Regulatory & ethics support

  • Clinical operations & logistics

  • Data management support

  • Pharmacovigilance support

  • Joint grant development

  • Possible internal funding (subject to approval)

Study Types Accepted

  • Feasibility Studies

  • Phase I – IV Clinical Studies

  • Pharmacovigilance Studies

Proposal Requirements

  • Project title & research summary

  • Therapeutic area & study phase

  • Background & problem statement

  • Study timeline

  • Objectives & research questions

  • Grant /funding plan

  • Partnership structure & roles

  • Timeline & Budget estimate

  • Team, roles & CVs

  • Target population & participant profile

  • Institutional & investigator experience

  • Study design & methodology

Selected applicants will be contacted within 4 weeks after the submission deadline. For more information and clarification, contact [email protected]

Submit your proposal

Send your completed submission to [email protected]
with the subject line: RFP Submission

About UCTSS

UCTSS is a Contract Research Organization (CRO) developing in-roads to conducting early and late phase clinical trials research in West Africa.We manage all site and patient recruitment activities on behalf of sponsors. Using local resources, we also manage all project activities as well as all aspects of regulatory processes, from submissions to approvals. Pharmacovigilance support, data management and analytics services are well managed by our competent teams.

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