Senior Clinical Research Associate

Ladders; United States; Remote; USD 111,000 - 138,000; Full time

Benefits offered by this job

Health and wellbeing

Retirement plans

Life insurance

Disability coverage

Wellbeing resources

Training programs

Job summary

Ladders is seeking a Senior Clinical Research Associate to support oncology trials across multiple sites in a remote US-based setting. You will monitor sites, ensure protocol adherence, and maintain GCP compliance while collaborating with cross-functional teams.

The role includes training site personnel, resolving issues promptly, and traveling as required to ensure trial progress and data quality.

Qualifications

• Advanced degree in life sciences, nursing, or medicine.
• Extensive CRA experience with trial processes and regulations.
• Proven ability to manage multiple sites and projects.
• Expertise in monitoring practices and clinical trial software.
• Oncology monitoring experience is mandatory.
• Willingness to travel at least 60% with a valid driver's license.

Responsibilities

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for accurate data reporting.
• Provide training and support to site staff and CRAs.
• Build and maintain relationships with site personnel and stakeholders.

Skills

Oncology monitoring experience

Site monitoring

GCP compliance

Education

Advanced degree in life sciences, nursing, or medicine

Job description

For our client, we are seeking a Senior Clinical Research Associate to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will support the execution of oncology clinical trials across multiple sites, with a strong focus on site monitoring, protocol adherence, and Good Clinical Practice (GCP) compliance. The Senior Clinical Research Associate will work closely with site teams and cross-functional stakeholders to help ensure data quality, resolve issues quickly, and keep studies moving forward. This position also includes training and supporting site personnel while building trusted relationships that contribute to trial success.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $110,520 - $138,150 annually

Responsibilities

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for accurate data reporting.
• Provide training and support to site staff and CRAs.
• Build and maintain relationships with site personnel and stakeholders.

Qualifications

• Advanced degree in life sciences, nursing, or medicine required.
• Extensive experience as a Clinical Research Associate (CRA) with knowledge of trial processes and regulations.
• Proven ability to manage multiple sites and projects with effective organizational skills.
• Expertise in monitoring practices and clinical trial software tools.
• Excellent communication and stakeholder management abilities.
• Oncology monitoring experience is mandatory.
• Willingness to travel at least 60% of the time, with a valid driver's license.

Benefits

• Competitive base salary and performance-related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training

Our client is an equal opportunity employer.