# R&D Study Operation Oncology CRA

Hiring organization: [Merck](https://career.thegoodapps.co/organizations/merck)

Canonical page: https://career.thegoodapps.co/jobs/80b9a423-0cac-485b-b5bc-758c5a01a851

Listed on Merck's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Mid

## Summary

This role oversees clinical trial operations for oncology drug development, managing investigator sites, recruitment, safety monitoring, and regulatory documentation. It suits experienced clinical research associates with oncology background who can coordinate between medical teams and company stakeholders.

_Our summary, not Merck's wording._

## Skills named

Clinical Data Management, Drug Development, Microsoft Excel, Microsoft Word, PowerPoint, Regulatory Compliance

## Required

- 4–5 years of oncology CRA experience
- Communication skills with physicians and clinical research coordinators
- Medical knowledge fundamentals
- Presentation ability to explain trial protocols and drug overviews
- Computer proficiency in Microsoft Office
- English proficiency (TOEIC 730+ for business email)
- Ability to work as part of internal project teams
- Ability to coordinate across global R&D departments

## Nice to have

- Knowledge of GCP and internal SOPs
- Knowledge of the assigned trial drug and disease area
- English conversation ability for presentations and teleconferences
- Specialist knowledge in oncology

Apply on Merck's site: https://msd.wd5.myworkdayjobs.com/en-US/SearchJobs/job/JPN---Tokyo---Chiyoda/R-D-Study-Operation-Oncology-CRA_R400034