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
Clinical Research Associate in chicago at Unknown Company
This position is listed as contract and onsite.