Senior CRA – Remote with Travel Contract

Actalent; San Diego (CA); Remote; USD 96,000 - 131,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) retirement plan

Life Insurance

Time Off / PTO

Job summary

Actalent is seeking a Clinical Research Associate (CRA) to manage and coordinate clinical monitoring and site management activities. This 100% home-based position involves remote or on-site visits to ensure protocol compliance, regulatory adherence, and high-quality data across trials.

The role requires ICH-GCP knowledge, strong communication, and the ability to work independently or in a team. A life sciences degree or RN license is required with 2+ years monitoring experience; travel will be

Qualifications

• Bachelor's degree in life sciences or RN required.
• Minimum 2+ years of experience as a clinical research monitor.
• Valid driver's license where applicable.
• Strong knowledge of ICH-GCP and regulatory guidelines.
• Excellent written and verbal communication skills.
• Ability to work independently or in a team.
• Proficient in Microsoft Office and learning CTMS/eClinical software.

Responsibilities

• Monitor investigator sites using a risk-based monitoring approach.
• Verify data accuracy via source data review and CRF review (on-site/remote).
• Assess investigational products through inventory and records review.
• Escalate deficiencies to clinical management for resolution.
• Maintain regular contact with sites to ensure protocol adherence.
• Participate in investigator meetings and site initiation.
• Ensure essential documents are complete per ICH-GCP guidelines.
• Support project team with publications/tools and process improvements.

Skills

Clinical monitoring

Site management

Risk-based monitoring

Root cause analysis

ICH-GCP

Regulatory compliance

Data accuracy

Documentation

Communication

Time management

MS Office

Education

Bachelor's in life sciences

Registered Nursing (RN)

Tools

CTMS

eClinical

Job description

Actalent is seeking a Clinical Research Associate (CRA) to manage and coordinate clinical monitoring and site management activities. This 100% home-based position involves remote or on-site visits to ensure protocol compliance, regulatory adherence, and high-quality data across trials.

The role requires ICH-GCP knowledge, strong communication, and the ability to work independently or in a team. A life sciences degree or RN license is required with 2+ years monitoring experience; travel will be