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Senior Clinical Research Associate, Dermatology & Rheumatology (North Central)

5+ years
Not Disclosed
10 Jan. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc 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

๐ŸŒŸ Now Hiring: Senior Clinical Research Associate - Dermatology & Rheumatology (North Central U.S.) ๐Ÿ‡บ๐Ÿ‡ธ

๐Ÿ’ผ Position: Senior Clinical Research Associate, Dermatology & Rheumatology
๐Ÿข Industry: CRO - Clinical Operations
๐Ÿ“ Location: North Central Regions (Illinois, Indiana, Michigan, Ohio, Wisconsin)
โณ Job Type: Full-time

๐Ÿ”Ž Job Overview

The Senior Clinical Research Associate (CRA) will monitor clinical trials across the North Central regions of the U.S., ensuring compliance with protocols, standard operating procedures (SOPs), ICH-GCP guidelines, and regulatory requirements. This role will focus on dermatology, providing an opportunity to develop expertise in this therapeutic area.

๐Ÿ”‘ Key Responsibilities

1. Clinical Monitoring

  • Conduct site qualification, initiation, monitoring, and close-out visits for research sites
  • Prepare site visit reports and follow-up letters
  • Build productive relationships with investigators and site staff to meet study objectives
  • Ensure on-site study drug storage, dispensing, and accountability

2. Lead CRA Responsibilities

  • Review and approve site visit reports
  • Track site visit metrics and escalate issues to project teams
  • Mentor CRAs and support the development of training materials
  • Conduct quality control visits with CRAs

๐Ÿ“Œ Requirements

๐ŸŽ“ Education:

  • B.Sc. in Clinical Research, Nursing, or equivalent experience

๐Ÿ›  Experience:

  • At least 5 years of on-site clinical monitoring experience in the biotechnology, pharmaceutical, or CRO industry

๐Ÿ’ป Skills:

  • Strong knowledge of ICH/GCP standards and regulatory requirements
  • Excellent verbal and written communication skills in English
  • Ability to prioritize and work under pressure while maintaining attention to detail
  • Experience in dermatology is a plus
  • Ability to travel approximately 65% of the time

๐ŸŽฏ Perks & Benefits

โœจ Home-based position with travel requirements
โœจ Work for a well-regarded CRO specializing in dermatology
โœจ Mentorship opportunities and career development

๐Ÿ“Œ Company: Innovaderm (Specialized in Dermatology CRO Research)

๐Ÿ“ฉ Apply Now!