Remote Quality Associate, Clinical Trials & Compliance

Real Staffing Group; Princeton (NJ); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Retirement savings plans

Life and disability insurance

Paid leave

Job summary

Real Staffing Group is seeking a Quality Associate for a remote, 12-month contract to oversee quality across multiple clinical trials from start-up to closeout. The role partners with clinical and cross-functional teams to support planning, execution, monitoring, and reporting of studies, while reviewing metrics and driving CAPA and continuous improvement initiatives.

The ideal candidate holds a Life Sciences-related degree with at least 4 years in clinical research or quality assurance, and is

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, Biostatistics, Clinical Research, or a related field.
• Minimum 4 years of experience in clinical research, quality assurance, GCP compliance, or related areas.
• Strong knowledge of ICH-GCP, FDA and EMA regulations, and global clinical trial requirements.
• Experience with data analysis, quality management systems, and Microsoft Office applications.
• Ability to work independently and manage multiple priorities.

Responsibilities

• Partner with clinical and cross-functional teams to support the planning, execution, monitoring, and reporting of clinical trials.
• Review quality metrics, operational data, and performance trends to identify risks, compliance issues, and process improvement opportunities.
• Assess protocol deviations, data integrity concerns, quality events, and noncompliance issues, escalating findings as needed.
• Support CAPA effectiveness reviews, audit and inspection follow-up activities, and risk-based quality management initiatives.
• Participate in audit planning, inspection readiness, quality documentation reviews, and continuous improvement efforts.
• Mentor junior team members and support onboarding and training activities.

Skills

ICH-GCP

FDA/EMA regulations

Clinical trial processes

Data integrity

Microsoft Office

Education

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, Biostatistics, Clinical Research, or a related field

Tools

TrackWise

eQMS

Job description

Real Staffing Group is seeking a Quality Associate for a remote, 12-month contract to oversee quality across multiple clinical trials from start-up to closeout. The role partners with clinical and cross-functional teams to support planning, execution, monitoring, and reporting of studies, while reviewing metrics and driving CAPA and continuous improvement initiatives.

The ideal candidate holds a Life Sciences-related degree with at least 4 years in clinical research or quality assurance, and is