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Senior Clinical Research Associate Medical Device Remote

2+ years
$129,000 to $138,000
10 Nov. 27, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Opportunity: Clinical Research Associate (West Coast USA – Remote)
Employer: Provident Research Inc.
Location: Remote (West Coast USA)
Industry: Medical Device
Employment Type: Full-Time
Travel Requirement: Regional travel up to 65%


About the Role

Provident Research Inc. is seeking a Clinical Research Associate (CRA) to join our team through a dedicated Functional Source (embed) relationship with a leading medical device manufacturer. This role focuses on overseeing and managing clinical activities at multiple study sites, fostering strong relationships with site personnel, and ensuring the success of clinical trials.

Interviews are ongoing for immediate openings due to team expansion.


Key Responsibilities

  • Manage clinical study activities across multiple sites within one or more clinical projects.
  • Conduct on-site visits in accordance with the monitoring plan and maintain compliance with ICH-GCP regulations.
  • Oversee site performance and ensure study protocols are adhered to.
  • Monitor patient safety on-site, addressing missing SAE/AE reports and protocol violations.
  • Build and maintain productive relationships with investigators and site staff.
  • Serve as the primary liaison between Clinical Operations and study site personnel.
  • Perform site-specific tasks such as facilities inspections, study training, and compliance monitoring.

Qualifications

Education:

  • Bachelor’s degree (required).

Experience:

  • Previous Medical Device experience (mandatory).
  • Experience with regional monitoring is required.
  • Proficiency in clinical research regulations and standards.

Certifications (Preferred):

  • CCRA, RAC, or CDE certifications.

Skills:

  • Strong leadership and organizational skills.
  • Excellent written and verbal communication.
  • High attention to detail.

Benefits

Provident Research Inc. offers competitive compensation and benefits, including:

  • Medical, Dental, and Vision insurance.
  • Disability and Life Insurance.
  • 401(k) Plan.
  • Paid vacation and holidays.
  • Opportunities for growth and internal promotions.

Why Join Provident Research Inc.?

This role offers an opportunity to engage in diverse aspects of the clinical development industry, providing a strong career pathway with exposure to cutting-edge medical device research.


If you're ready to make an impact in the medical device clinical research field, we encourage you to apply now and join the movement at Provident Research Inc.