Clinical Research Assistant – Dermatology Trials (Phase I-III)

Eurofins; Forest (VA); On-site; USD 29,000 - 32,000; Full time

Benefits offered by this job

Excellent full-time benefits including

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Consumer Product Testing seeks a Clinical Research Assistant to support Phase I-III IND trials evaluating hair, skin and nails. Training is provided and regulatory experience is a plus.

You will work with two Principal Investigators in Dermatology and perform study planning, documentation, and record-keeping. Responsibilities include audits, IRB submissions, participant recruitment, visits, vitals, data entry and PI assistance.

Qualifications

• Certified CRA credential ideal.
• Minimum 1+ years experience in clinical research.
• Experience in regulatory aspects of Phase I-III IND trials and FDA audits.
• Experience with Microsoft platforms, EMR and EHR systems; CTMS strongly preferred.
• Authorization to work in the United States without sponsorship.

Responsibilities

• Project support including planning, paperwork, and maintaining study participant records.
• Conduct audits (virtual and in person) and assist with study preparation and closing.
• Work with IRB submissions and participant recruitment including screening and scheduling.
• Execute study visits with vitals, data entry, and PI assistance.
• Support the Clinical Manager and adapt to business needs.

Skills

Microsoft platforms

EMR/EHR systems

CTMS

Phlebotomy

Education

Certified CRA credential ideal

Minimum 1+ years experience in clinical research

Tools

CTMS

EMR/EHR

Job description

Eurofins USA Consumer Product Testing seeks a Clinical Research Assistant to support Phase I-III IND trials evaluating hair, skin and nails. Training is provided and regulatory experience is a plus.

You will work with two Principal Investigators in Dermatology and perform study planning, documentation, and record-keeping. Responsibilities include audits, IRB submissions, participant recruitment, visits, vitals, data entry and PI assistance.