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Sr Cra - Oncology - Fsp - North Central & West Coast

3+ years
$115K–$140K
10 Oct. 6, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Sr CRA – Oncology – FSP (North Central & West Coast)

Locations:
9 major hub locations in North Central (IL, MN, MO, IA, KS) and West Coast (CA, AZ)

Category: Clinical
Job ID: 254284
Target Pay Range: $115K–$140K
Work Mode: Remote (#LI - Remote)


Job Overview

The Sr CRA will utilize clinical expertise and judgment to ensure a high standard of care for trial participants and respond to emergency situations according to clinical research standards. This role involves site monitoring, site management, data integrity assurance, and adherence to regulatory requirements for oncology studies.


Primary Responsibilities

Site Monitoring & Management:

  • Conduct routine and close-out monitoring of clinical sites.

  • Maintain study files and perform pre-study and initiation visits.

  • Liaise with vendors as needed.

  • Manage all aspects of site operations as outlined in project plans.

  • Undertake feasibility assessments when requested.

General On-Site Monitoring:

  • Ensure study staff have the necessary materials and instructions to enroll participants safely.

  • Verify adherence to informed consent procedures and protocol requirements.

  • Maintain the integrity of data submitted on CRFs or other collection tools.

  • Monitor data for missing or implausible entries.

  • Manage registry administration as per project plans.

Safety & Data Management:

  • Complete SAE reporting, generate narratives, and follow up on SAEs.

  • Independently perform CRF review, query generation, and resolution using established guidelines on Fortrea or client data management systems.

Team Support & Coordination:

  • Assist in training new employees (e.g., co-monitoring).

  • Coordinate designated clinical projects as a Local Project Coordinator and act as a local client contact if applicable.

  • Perform other duties as assigned by management.


Qualifications / Skills

Minimum Required:

  • University or college degree, or certification in a related allied health profession (e.g., nursing licensure).

  • 3+ years of onsite clinical monitoring experience.

  • Oncology clinical trial experience.

  • Strong teamwork and communication skills.

  • Comfortable in a fast-paced, technology-driven, and dynamic work environment.

Preferred:

  • Experience working in major hub locations in the US.

  • Proficiency with electronic data capture systems.


Work Environment & Culture

  • Fast-paced with strict adherence to study protocols and timelines.

  • Frequently changing priorities requiring adaptability.

  • Emphasis on teamwork and effective collaboration.

  • Technology-based environment for direct electronic data capture.


Benefits

  • Comprehensive benefits for regular full-time or part-time employees (20+ hours/week) including:

    • Medical, Dental, Vision, Life, STD/LTD insurance

    • 401(K) plan

    • Paid Time Off (PTO) – Flex Plan

    • Employee recognition awards

    • Multiple Employee Resource Groups (ERGs)