Clinical Researcher

Title: Full-Time Clinical Researcher - Medical Research

About us: A leading healthcare group delivering high-impact clinical research and publications.

You will

• Conduct rapid/systematic reviews (PRISMA)
• Draft protocols and IRB submissions
• Clean/analyze data (R/Python/SPSS/Stata)
• Create publication-grade figures/tables
• Format/submit to journals; manage revisions
• Maintain EndNote/Zotero libraries

You have: MSc/PhD (epi/biostats/public health/biomedical sciences) or strong publication record; solid statistics; excellent academic writing; EndNote/Zotero.

Offer: Competitive base + performance bonus; conference/training budget; growth path to Research Lead.

Location: Riyadh (hybrid/remote within UTC+3 possible).

Apply with: CV, two writing samples, analysis/code sample, and Google Scholar/ORCID.

Extended Version

Role purpose: Own the end-to-end research pipeline: evidence synthesis, protocol/IRB, data analysis, figures/tables, submission through acceptance.

Key responsibilities

• Rapid + systematic reviews (PRISMA), evidence tables, executive briefs
• Protocols, consent forms, IRB packages; renewals/amendments
• Data cleaning/analysis; appropriate models; publication-grade figures/tables
• Manuscript preparation/submission; reviewer responses and revisions
• EndNote/Zotero per Vancouver/ICMJE; version control for drafts/data
• Reusable slide/figure library for updates and talks.

Required qualifications

• MSc/PhD or equivalent track record; statistics (R/Python; SPSS/Stata acceptable)
• Strong academic writing; reliable on deadlines
• Familiar with PRISMA/CONSORT/ICMJE; reference management

Success metrics (first 90 days) Tracker + SOPs; one IRB/renewal; one manuscript draft or revision; monthly evidence brief.

Compensation & benefits: Competitive base; performance bonus; professional development budget; modern tooling.