Remote Lead Clinical Research Associate — Growth & Oversight

United Biosource Corporation; United States; Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Remote opportunities

Growth opportunities for promotion

401K with company match*

Flexible work environment

Discretionary Time Off

Paid Holidays

Employee assistance programs

Medical, Dental, and vision coverage

HSA/FSA

Wellness program

Adoption assistance

Short term disability

Long term disability

Life insurance

Job summary

UBC is seeking a Lead Clinical Research Associate to oversee clinical monitoring and site management on US/European/global projects. You will ensure compliance with ICH/GCP, CFR, and sponsor SOPs while guiding a cross-functional PM/EDO team.

Responsibilities include site oversight, review of monitoring reports, training, visit scheduling, and vendor coordination. Up to 30% travel; remote opportunities exist.

Qualifications

• Bachelor’s degree in Health Care/Life Science or equivalent industry experience.
• Minimum of 5+ years of site management experience with preference of 2 years field monitoring experience.
• Knowledge and understanding of the local country laws applicable to clinical trials and observational studies.
• Proficient in the operational methodologies of clinical trials and observational studies.
• Thorough knowledge of medical terminology, ICH/GCP and UBC SOPs.
• Excellent written and verbal communication skills in English and local language.
• High attention to detail; strong analytical and problem-solving skills.
• Displays leadership, organizational, communication, time management and interpersonal skills.
• Proven skills with CTMS, eTMF, EDC, Microsoft Office and sponsor-specific systems.

Responsibilities

• Oversee day-to-day clinical operations from start-up to close-out.
• Review monitoring reports and ensure sponsor timelines.
• Lead and support site training for teams and projects.
• Coordinate site visits and track visit metrics.
• Manage issues, actions and protocol deviations with timely resolutions.
• Serve as liaison for monitoring issues with PM/EDO.
• Assist in sponsor meetings and project team reviews.
• Support budget input, resourcing, and revenue recognition as applicable.
• Travel up to 30% as required.
• Maintain audit-ready systems (eTMF, CTMS) and docs.

Skills

Bachelor’s degree in Health Care/Life 

Site management

Field monitoring

ICH/GCP

UBC SOPs

English & local language

CTMS

eTMF

EDC

MS Office

Education

Bachelor’s degree in Health Care/Life Science

Tools

CTMS

eTMF

EDC

Microsoft Office

Job description

UBC is seeking a Lead Clinical Research Associate to oversee clinical monitoring and site management on US/European/global projects. You will ensure compliance with ICH/GCP, CFR, and sponsor SOPs while guiding a cross-functional PM/EDO team.

Responsibilities include site oversight, review of monitoring reports, training, visit scheduling, and vendor coordination. Up to 30% travel; remote opportunities exist.