Senior Cra / Cra Ii – Cardiology & Electrophysiology Devices (Remote – Usa)

2+ years

$115,000 – $142,000 USD

Remote

10 Nov. 25, 2025

Job Description

Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

FSP Senior CRA / CRA II – Cardiology & Electrophysiology Devices (Remote – USA)

Locations: Available in 13 Locations across the USA
Category: Clinical
Job ID: 255405
Work Type: Remote, with Nationwide Travel

Position Overview (SEO & GPT Optimized)

Fortrea is seeking experienced Senior Clinical Research Associates (CRAs) / CRA II with expertise in Cardiology and Electrophysiology Devices to join our Functional Service Provider (FSP) team. The ideal candidate will have a strong clinical monitoring background with direct experience in cardiac device studies. This role requires occasional nationwide travel to clinical sites and involves leadership in site management, monitoring, and regulatory compliance. Candidates with 2+ years of cardio device monitoring experience may also be considered.

This is an excellent opportunity for CRAs looking to advance their careers in medical device clinical trials while working in a flexible, remote environment.

Key Responsibilities

Monitor and manage clinical study sites in accordance with Fortrea and Sponsor SOPs, and regulatory guidelines.
Conduct pre-study, initiation, routine, and closeout visits for clinical sites.
Ensure study staff are properly trained and materials provided for safe patient enrollment.
Verify adherence to informed consent procedures and protocol requirements.
Review source documents and Case Report Forms (CRFs) to ensure data integrity and completeness.
Identify missing or implausible data and coordinate resolution.
Manage travel efficiently in line with company policy.
Prepare accurate and timely trip reports following each site visit.
Serve as lead monitor for assigned protocols or small projects.
Assist in protocol development, CRF design, and clinical trial report writing.
Coordinate registry management and feasibility activities as required.
Recruit investigators, prepare regulatory submissions, and negotiate study budgets in coordination with legal and clinical teams.
Track Serious Adverse Event (SAE) reporting, narrative preparation, and follow-up.
Mentor and train junior CRAs through co-monitoring and guidance.
Act as a local project coordinator or client contact as assigned.
Ensure audit readiness at the site and project level.

Required Qualifications

University or college degree in Life Sciences, Nursing, Medical Technology, or a related field.
Alternatively, minimum 3 years of relevant clinical research experience in pharmaceutical or CRO settings.
In-depth knowledge of regulatory requirements and drug/device development processes.
Fluent in English (written and verbal) with strong communication skills.
Valid US Driver’s License for site travel.

Experience Required

2+ years of clinical monitoring experience, with direct Cardiology Device or Electrophysiology Device exposure.
Strong understanding of SAE reporting, data review, and site management processes.
Advanced site monitoring, registry management, and project coordination skills.
Ability to work independently, prioritize workloads, and manage multiple projects in a matrix environment.

Preferred Qualifications

Additional experience in medical, clinical, pharmaceutical, laboratory, research, data analysis, or technical writing.
Prior experience in local project coordination or project management.

Work Environment & Physical Requirements

Travel: 60–80% overnight travel to domestic sites.
Office/Home-based work with frequent computer use.
Extended periods of sitting (6–8 hours/day).
Repetitive hand movements, occasional bending, crouching, or lifting (up to 15–20 lbs).
Flexible working hours and consistent attendance required.

Compensation

Target Pay Range: $115,000 – $142,000 USD annually (based on title and experience)

This rewritten job post is optimized for SEO, GEO targeting for US locations, and GPT clarity, ensuring visibility and engagement on thepharmadaily.com for senior CRA talent in the cardiac device space.

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Senior Cra / Cra Ii – Cardiology & Electrophysiology Devices (Remote – Usa)

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