Senior Clinical Research Associate (CRA) – Dermatology & Rheumatology | USA (Midwest Region)
Company: Indero
Location: Remote, United States (Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, Wisconsin)
Employment Type: Permanent | Full-Time
Industry: Clinical Research | CRO | Dermatology | Rheumatology
Experience Required: Minimum 5+ years of on-site clinical monitoring experience in biotech, pharmaceutical, or CRO settings
Role Overview
A globally recognized dermatology and rheumatology-focused Contract Research Organization (CRO) is hiring a Senior Clinical Research Associate (CRA) to support clinical trials across the U.S. Midwest region. This remote-based role requires extensive regional travel and offers the opportunity to deepen therapeutic expertise in dermatology and rheumatology clinical research.
The Senior CRA will oversee clinical trial monitoring activities to ensure studies are conducted in compliance with study protocols, sponsor SOPs, ICH-GCP guidelines, and all applicable U.S. regulatory requirements.
This opportunity is ideal for experienced CRAs who excel in autonomous work environments, consistently deliver high-quality outcomes, and seek to contribute meaningfully within a specialized CRO.
Key Responsibilities
Conduct site qualification, initiation, routine 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 procedures.
Review essential regulatory documentation and ensure completeness and accuracy.
Prepare comprehensive site visit reports and follow-up correspondence.
Participate in investigator meetings and sponsor discussions.
Develop strong relationships with investigators and site staff to support patient recruitment and retention targets.
Ensure data integrity, patient safety, and adherence to regulatory standards.
Lead CRA Responsibilities (As Applicable)
Review and approve monitoring visit reports.
Track site performance metrics and escalate risks to project teams.
Support development of clinical monitoring plans and annotated visit templates.
Mentor junior CRAs and contribute to CRA training initiatives.
Conduct on-site quality control visits.
Collaborate with project management teams 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 independent on-site monitoring experience within biotechnology, pharmaceutical, or CRO environments.
Prior exposure to rheumatology clinical trials required.
Experience in dermatology clinical research is highly preferred.
Core Competencies & Skills
Strong knowledge of ICH-GCP standards and U.S. regulatory requirements.
Excellent written and verbal communication skills in English.
Demonstrated ability to manage multiple clinical trials and prioritize competing deadlines.
Strong critical thinking and problem-solving abilities.
High attention to detail and commitment to quality assurance.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
Ability to travel approximately 65% within assigned states.
About the Organization
Indero is a global clinical research leader specializing in dermatology and rheumatology. With more than 25 years of experience, the organization delivers full-service CRO solutions including protocol design, site selection, patient recruitment, clinical monitoring, biometrics, pharmacovigilance, and regulatory consulting.
With operational capabilities across North America, Europe, Asia Pacific, and Latin America, the organization partners with biotech and pharmaceutical sponsors to deliver scientifically rigorous and operationally efficient clinical trials worldwide.
Work Culture & Growth
The organization fosters a collaborative, innovation-driven environment where clinical expertise is recognized and career development is supported. Employees benefit from working within a specialized therapeutic focus while contributing to global clinical advancements.
Equal Opportunity Statement
The organization is committed to equitable treatment and equal opportunity for all applicants. Reasonable accommodations are available during the recruitment process upon request.
Applicants must be legally authorized to work in the United States.
Apply via ThePharmaDaily.com
If you are an experienced Senior Clinical Research Associate with rheumatology and dermatology expertise seeking a remote Midwest-based CRO opportunity, apply now through ThePharmaDaily.com to advance your career in specialized clinical trial monitoring and regulatory-compliant research execution.
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