Senior Clinical Research Associate - Haematology

About the Role

Upsilon Global is looking for experienced freelance Senior Clinical Research Associates (SCRAs) based in the United States to provide support for a specialist Contract Research Organization (CRO) focused on haematology clinical trials. The client is initiating a Phase II haematology study and intends to onboard three freelance SCRAs promptly.

Key Details

• Position: Freelance Senior Clinical Research Associate (SCRA)
• Location: United States
• Contract Type: 1099 Contractor
• Full-time Equivalent: Up to 1.0 FTE depending on monthly workload
• Start Date: Immediate availability preferred
• Travel: Site assignments will be regionally allocated based on your location within the USA

Primary Responsibilities

• Perform on-site monitoring visits in alignment with the study protocol, ICH-GCP guidelines, SOPs, and all relevant regulatory standards.
• Conduct source data verification and review study documentation thoroughly to ensure clinical trial data accuracy and integrity.
• Establish and foster strong working relationships with investigators and site teams to facilitate effective study execution.
• Provide support throughout site initiation, routine monitoring, and study close-out procedures.
• Safeguard subject safety by overseeing adverse event reporting and confirming appropriate follow-up measures.
• Identify, document, and resolve site-related issues, keeping the project team informed with timely updates.
• Assist with regulatory inspections and audits from sponsors when necessary.
• Maintain comprehensive and precise trial documentation, including essential documents and monitoring reports.
• Remain up to date with current regulations, industry guidance, and best clinical research practices.

Candidate Requirements

• Minimum of five years' experience monitoring clinical trials independently as a CRA.
• Essential experience in haematology clinical trials.
• Solid knowledge of United States clinical trial regulations, including ICH-GCP and FDA requirements.
• Proven capability to manage clinical sites independently from start-up through study close-out.
• Strong organizational, communication, and analytical problem-solving skills.
• Ability to work autonomously in a dynamic setting while managing multiple priorities effectively.
• Willingness to travel extensively within your designated regional area across the USA.