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Sr Cra I Or Cra 2 - Oncology - Fsp West Region (Northern Ca, Nv, Az, Id, Nm, Or, Wa, Co)

3+ years
$120K–$133K
10 Oct. 6, 2025
Job Description
Job Type: Full Time 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 I / CRA 2 – Oncology (FSP West Region)

Locations: Northern CA, NV, AZ, ID, NM, OR, WA, CO
Category: Clinical
Job ID: 254563
Travel Requirements: 60–80% overnight
Target Pay Range: $120K–$133K


Job Overview

Responsible for site monitoring and site management for oncology clinical studies in accordance with Fortrea and/or Sponsor SOPs and regulatory guidelines. Functions as a lead or local project coordinator as assigned and ensures implementation of project plans with quality and compliance.


Primary Responsibilities

Site Monitoring & Management

  • Conduct routine and closeout monitoring of clinical sites.

  • Ensure study staff receive proper training and protocol instructions.

  • Verify patient protection through adherence to informed consent procedures and protocol requirements.

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

  • Monitor data for missing or implausible entries.

  • Manage monitoring tasks efficiently and cost-effectively according to SOPs and travel policies.

  • Ensure site audit readiness.

  • Prepare accurate and timely monitoring trip reports.

Project Coordination & Leadership

  • Serve as lead monitor or Local Project Coordinator as assigned.

  • Manage small projects under Project Manager/Director supervision.

  • Review project progress and take action to achieve objectives.

  • Organize and present at Investigator Meetings.

  • Participate in protocol and CRF development.

  • Contribute to clinical trial report writing.

  • Coordinate with internal work groups and vendors as needed.

  • Conduct feasibility assessments and QC visits as requested.

  • Negotiate study budgets and assist legal team with agreements.

  • Track, report, and follow-up on Serious Adverse Events (SAEs).

  • Perform CRF review, query generation, and resolution.

  • Assist with training, mentoring, and development of junior staff.

  • Perform other duties as assigned by management.


Qualifications / Skills

  • University/college degree (life sciences preferred) or certification in allied health, nursing, medical, or lab technology.

  • Minimum 3 years of relevant clinical research experience in pharmaceutical or CRO industries considered if degree is not held.

  • Thorough knowledge of regulatory requirements and drug development process.

  • Fluency in local office language and English (written and verbal).

  • Advanced site monitoring, site management, and registry administration skills.

  • SAE reporting knowledge.

  • Strong planning, organizational, and computer skills.

  • Ability to train and supervise junior staff.

  • Ability to work independently and within a matrix project team.

  • Valid Driver's License.


Preferred Qualifications

  • 1+ year additional experience in medical, clinical, pharmaceutical, laboratory, research, data analysis, or technical writing.

  • Local project coordination and/or project management experience.


Physical Demands / Work Environment

  • Frequent overnight travel (60–80%).