Senior Clinical Research Associate II

Location: United States – New York – New York City. Significant travel of 60–80% within the cluster is required, with possible international and weekend travel.

Annual base salary: $99,200–$165,400, plus a 12.5% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global develops pharmaceutical products and conducts global clinical research programs.

What you will do

• Manage investigator sites from site initiation through routine monitoring, database lock, and close-out.
• Ensure clinical trials follow monitoring plans, applicable laws, ICH/GCP requirements, and hirify.global standards.
• Serve as the primary contact for assigned sites and coordinate information flow among investigators, vendors, and study teams.
• Support site enrollment, recruitment initiatives, protocol training, patient safety, and resolution of adverse-event and serious-adverse-event reporting issues.
• Track trial documentation, recruitment, clinical supplies, study metrics, data queries, protocol deviations, and investigational product accountability.
• Identify site risks, implement corrective and preventive actions, support audits and inspections, and mentor CRAs.

Requirements

• Bachelor’s or professional degree in life sciences, nursing, pharmacy, medicine, or an equivalent field.
• At least five years of relevant clinical research site-monitoring experience; oncology experience is preferred.
• Extensive knowledge of clinical trial methodology, ICH/GCP, FDA requirements, and local regulations.
• Experience with global clinical trials, site management, monitoring, data acquisition and cleaning, reporting, protocol design, and feasibility assessment.
• Ability to work in matrix teams, influence stakeholders, manage complex risks, and mentor monitoring professionals.
• Fluent English and the native language or languages of the country of work are required. Candidates must have permanent authorization to work in the United States; U.S. visa sponsorship is not available.

Nice to have

• Three or more years of oncology monitoring experience.
• Therapeutic experience in vaccines, internal medicine, or infectious diseases.
• Experience as an unblinded monitor or Site Care Partner.

Culture & Benefits

• Full-time employment with a performance bonus and share-based long-term incentive eligibility.
• 401(k) plan with hirify.global matching contributions and an additional retirement savings contribution.
• Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
• Medical, prescription drug, dental, and vision coverage.
• Relocation assistance may be available based on business needs and eligibility.