Clinical Research Associate II

TL;DR

Clinical Research Associate II (Oncology): Monitor and own the progress of clinical studies at investigative sites ensuring they are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and regulations with an accent on study setup, site initiation, and risk mitigation. Focus on coordinating investigator identification, regulatory submissions, pre-study visits, and proposing solutions for potential study risks.

Location: Remote, fully home-based in the United Kingdom. Availability for domestic travel up to 50-60% including overnight stays.

Company

hirify.global is a CRO focused on precision medicine, combining clinical trial designs, biomarker analytics, and expertise in oncology and rare diseases.

What you will do

• Monitor clinical studies at sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
• Coordinate study setup activities including investigator identification, regulatory submissions, pre-study, and initiation visits.
• Identify potential study risks and propose mitigation solutions.
• Own study progress, quality, and outcomes.
• Handle site visits, investigator meetings, and project team updates.

Requirements

• Fluency in English.
• 4-year college degree or equivalent experience.
• More than 1 year CRA experience in CRO or pharmaceutical industry.
• Availability for up to 50-60% domestic travel including overnight stays (international for senior roles).
• Calm, detail-oriented, proactive in risk identification and conflict resolution.

Nice to have

• Oncology experience.
• Early phase experience.

Culture & Benefits

• Lower than average number of protocols for deeper expertise.
• Reasonable travel supporting work/life balance.
• Direct line management support and influence in a smaller CRO.
• High CRA retention due to culture and people.
• Voice heard with impact on company decisions.