Company: Indero (formerly Innovaderm)
Location: Arizona, Nevada, Oregon – USA (Remote-Based with Regional Travel)
Employment Type: Permanent | Full-Time
Industry: Clinical Research | CRO | Dermatology | Rheumatology
Experience Required: Minimum 5+ years of on-site clinical monitoring experience in biotechnology, pharmaceutical, or CRO environments
Role Overview
A global dermatology-focused Contract Research Organization (CRO) is seeking an experienced Senior Clinical Research Associate (CRA) to support clinical trials across Arizona, Nevada, and Oregon. This remote-based role requires regional travel and offers the opportunity to specialize in dermatology and rheumatology clinical research.
The Senior CRA will ensure that clinical trials are conducted, monitored, and reported in compliance with study protocols, ICH-GCP guidelines, sponsor SOPs, and applicable U.S. regulatory requirements. This role is ideal for independent CRAs who thrive in autonomous environments while maintaining high standards of quality and regulatory compliance.
Key Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits in accordance with monitoring plans and regulatory standards.
Perform source data verification (SDV) and ensure protocol compliance.
Verify investigational product storage, dispensing, and accountability.
Review regulatory documentation and ensure completeness and accuracy.
Prepare detailed site visit reports and follow-up communications.
Participate in investigator meetings and sponsor discussions.
Build strong working relationships with investigators and site staff to support enrollment and retention goals.
Ensure data accuracy, patient safety, and overall study integrity.
Lead CRA Responsibilities (As Applicable)
Review and approve monitoring visit reports.
Track monitoring metrics and escalate risks to project teams.
Contribute to the development of clinical monitoring plans and tools.
Support training initiatives for CRAs.
Mentor junior CRAs and conduct on-site quality control visits.
Collaborate with project managers to resolve operational challenges.
Required Qualifications
Education:
Bachelor’s degree in Life Sciences, Nursing, or a related clinical research discipline.
Equivalent clinical research experience may be considered.
Experience:
Minimum 5+ years of on-site monitoring experience within biotechnology, pharmaceutical, or CRO industries.
Strong experience conducting independent monitoring visits.
Experience in dermatology clinical trials is highly preferred.
Core Competencies & Skills
Strong knowledge of ICH-GCP guidelines and U.S. regulatory requirements.
Excellent written and verbal communication skills in English.
Proven ability to manage multiple studies and prioritize tasks under tight timelines.
Strong analytical thinking, problem-solving, and decision-making skills.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
Ability to travel approximately 65% regionally within assigned states.
High attention to detail and commitment to clinical trial quality standards.
About the Organization
Indero is a globally recognized CRO specializing in dermatology and rheumatology clinical research. With more than 25 years of experience, the organization delivers full-service clinical trial solutions, including protocol development, patient recruitment, monitoring, biometrics, pharmacovigilance, and regulatory consulting.
With operational capabilities across North America, Europe, Asia Pacific, and Latin America, the company partners with biotechnology and pharmaceutical sponsors to advance innovative therapies efficiently and compliantly.
Work Environment & Culture
Employees benefit from a collaborative and innovation-driven environment where expertise in dermatology and rheumatology is highly valued. The organization emphasizes scientific rigor, operational excellence, and professional development opportunities.
Equal Opportunity Statement
The organization is committed to equitable treatment and equal opportunity for all applicants. Reasonable accommodations are available throughout the recruitment process for individuals with disabilities.
Applicants must be legally authorized to work in the United States.
Apply via ThePharmaDaily.com
If you are a seasoned Clinical Research Associate seeking to specialize in dermatology and rheumatology trials within a globally recognized CRO, apply now through ThePharmaDaily.com to advance your career in clinical monitoring and regulatory-compliant trial execution.
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