(Snr) Clinical Research Associate

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Requirements:

• Life science degree and / or equivalent experience
• CRA experience within the CRO or pharmaceutical industry (and working in Oncology). We require a minimum of 1 year experience as a CRA in Oncology, and can offer CRA II and Senior CRA titles depending on experience level.
• Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)

Responsibilities:

• Monitor and own 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.).
• Support Project Managers with trials that are larger in scope.
• Train and mentor junior staff members.
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.