Senior CRA - Dermatology & Rheumatology, Remote

Indero (formerly Innovaderm); Portland (OR); Remote; USD 85,000 - 110,000; Full time

Benefits offered by this job

Permanent full-time position

Vacation, sick days, 401K, Benefits

Teleworking allowance for travel

Ongoing learning and development

Job summary

Indero is seeking a Senior Clinical Research Associate to monitor dermatology and rheumatology studies across the Northwest and broader Western US. The role combines on-site and remote monitoring to ensure trials adhere to protocol, SOPs, ICH-GCP, and regulatory requirements.

The ideal candidate has 5–8 years of on-site monitoring experience, a B.Sc. in a related field, and strong English communication skills. Travel ~65% and a supportive, growth-oriented work environment are offered.

Qualifications

• Strong knowledge of ICH-GCP standards and regulatory requirements.
• Excellent verbal and written English communication.
• Ability to prioritize competing tasks and meet deadlines.
• Willingness to travel approximately 65% of the time.
• Proficiency with MS Office applications (Word, Excel, PowerPoint).
• Experience in dermatology is an asset.

Responsibilities

• Monitor clinical study progress at sites or remotely to ensure protocol compliance and high data quality.
• Prepare site visit reports and follow-up correspondence with investigators.
• Coordinate site qualification, initiation, monitoring and close-out visits per SOPs and regulations.
• Foster productive relationships with investigators and study staff to support recruitment and study objectives.

Skills

ICH-GCP knowledge

English proficiency

Time management

Attention to detail

Problem solving

Travel 65%

Education

B.Sc. in clinical research or related field

Tools

Microsoft Office

Job description

Indero is seeking a Senior Clinical Research Associate to monitor dermatology and rheumatology studies across the Northwest and broader Western US. The role combines on-site and remote monitoring to ensure trials adhere to protocol, SOPs, ICH-GCP, and regulatory requirements.

The ideal candidate has 5–8 years of on-site monitoring experience, a B.Sc. in a related field, and strong English communication skills. Travel ~65% and a supportive, growth-oriented work environment are offered.