Senior CRA, Oncology - 177305

Piper Companies; United States; À distance; USD 120 000 - 145 000; Plein temps

Avantages offerts par ce poste

Medical benefits

401k

Résumé du poste

Piper Companies is actively seeking Clinical Research Associates to join a top-tier CRO. This role is fully remote but requires travel 60-80% regionally on the West Coast.

The CRA serves as the primary bridge between sponsors and sites, ensuring trials follow protocols, protect patients, and meet regulatory expectations to help deliver lifesaving therapies. Ideal candidates have 3+ years of on-site monitoring in Oncology, familiarity with FDA processes, and a life sciences degree.

Qualifications

• 3+ years of on-site clinical monitoring experience, preferably in Oncology.
• Familiarity with FDA or equivalent regulatory bodies and accrediting administrations.
• Experience in a CRO environment is a plus.

Responsabilités

• Oversee development and execution of clinical trial plans for Phases I–IV.
• Maintain documentation and data evaluations.
• Collaborate with the team to ensure monitoring activities meet study requirements.
• Conduct on-site field evaluations.

Connaissances

On-site monitoring

Oncology

Communication skills

Formation

Bachelor’s degree in life sciences

Description du poste

Piper Companies is actively seeking Clinical Research Associates 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 West Coast. The Clinical Research Associate will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to succesffuly create lifesaving drugs and treatments

Responsibilities of the Clinical Research Associate:

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

Qualifications of the Clinical Research Associate:

• 3+ years of on-site clinical monitoring experience, specifically within Oncology
• Experience with the FDA or similar Regulatory and Accrediting administrations
• Bachelor’s degree in one of the life sciences or related background
• Prior experinece at a larger CRO preferred

Compensation for the Clinical Research Associate:

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

This job opens for applications on 8/21. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research Associate, CRA, BA, life sciences, clinical trials, phases, documentation, data, monitor, study, onsite, FDA, drugs, treatments, medical, dental, vision, oncology, tumor, cancer, 401k, PTO, Holiday,

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