Clinical Research Associate II - 177300

Piper Companies; Raleigh (NC); Remote; USD 120,000 - 145,000; Full time

Job summary

Piper Companies is seeking a Clinical Research Associate II for a fully remote role with 60-80% regional travel on the East Coast. You will serve as the primary bridge between sponsors and sites, ensuring trials follow protocols, protect patients, and meet regulatory expectations to successfully advance lifesaving therapies.

Responsibilities include developing and executing trial plans, maintaining documentation, coordinating with teams to ensure monitoring activities meet requirements, and

Qualifications

• 3+ years of on-site clinical monitoring experience within General Medicine or related therapeutic areas.
• Experience with the FDA or similar regulatory and accrediting agencies.
• Bachelor's degree in Life Sciences or a related field.
• Prior experience at a larger CRO preferred.

Responsibilities

• Oversee the development and execution of clinical trial plans and protocols for Phase I-IV studies.
• Maintain documentation and data evaluations.
• Work collaboratively with the team to ensure monitoring activities meet study requirements.
• Conduct on-site monitoring visits and field evaluations.

Skills

On-site monitoring

Regulatory compliance

Clinical trial monitoring

FDA familiarity

Education

Bachelor's degree in Life Sciences

Job description

Piper Companies is actively seeking Clinical Research Associates II to join a top-tier CRO with a proven track record of excellence, trusted by global pharma and biotech partners. This position is fully remote but does require travel 60-80% of the time regionally on the East Coast. The Clinical Research Associate II will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to successfully create lifesaving drugs and treatments.

Responsibilities of the Clinical Research Associate II:

• Oversee the development and execution of clinical trial plans and protocols for Phase I-IV studies
• Maintain documentation and data evaluations
• Work collaboratively with the team to ensure monitoring activities meet study requirements
• Conduct on-site monitoring visits and field evaluations

Qualifications of the Clinical Research Associate II:

• 3+ years of on-site clinical monitoring experience within General Medicine or related therapeutic areas
• Experience with the FDA or similar regulatory and accrediting agencies
• Bachelor's degree in Life Sciences or a related field
• Prior experience at a larger CRO preferred

Compensation for the Clinical Research Associate II:

• Salary Range: $120,000-$145,000
• Comprehensive Benefits: Medical, Dental, Vision, 401(k), PTO, bonuses, and sick leave if required by law

This job opens for applications on 10/16. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research Associate, CRA II, CRA, Clinical Monitoring, General Medicine, Clinical Trials, Phase I, Phase II, Phase III, Phase IV, Site Monitoring, FDA, CRO, Drug Development, Regulatory Compliance, Life Sciences, Pharmaceuticals, Biotechnology, Medical, Dental, Vision, 401(k), PTO, Holidays

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