Precision for Medicine is experiencing client growth and needs to hire experienced Clinical Research Associates (CRAs) to monitor oncology clinical studies.
Requirements
- 2+ years CRA experience within the CRO or pharmaceutical industry to be considered for a CRA II. 4+ year of CRA experience within the CRO or pharmaceutical industry to be considered for a Sr. CRA.
- Experience in monitoring oncology
- Availability for domestic travel including overnight stays, up to approximately 50-60% travel commitment (potential international travel may be required for some senior level positions)
- Fluency in English and for non-English speaking countries the local language of country where position based
Responsibilities
- You will 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.
- You will 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.).
- You will work with 2-3 protocols on average and support Project Managers with trials that are larger in scope.
- You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Other
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit, or project team update, you are always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
