Clinical Research Associate

Upsilon Global are seeking freelance SCRAs to support a major oncology programme for multiple myeloma, covering 60 sites across North America. This is large project roll-out with multiple CRAs needed across the country.

This will be an initial 12-month assignment, renewable annually with the potential to run until 2029.

A background in oncology/haematology is essential and, whilst full protocol training will be provided, prior multiple myeloma experience will be beneficial.

Quick info:

Company: Small CRO

Indication: Haematology/Oncology

FTE: Flexible contracts/FTE, but up to 1.0 fte available per contract

Duration: 12 months

Start: Asap

Responsibilities:

• Monitor and manage the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
• Work closely with project team, sites and study CRAs to coordinate IMV plan and site management activities

Requirements:

• CRA experience within the CRO or pharmaceutical industry; 2+ years
• Haematology-oncology experience is essential
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment

For more details please apply via the link or contact