Clinical Research Associate II/Sr. Clinical Research Associate

Precision for Medicine is not your typical CRO. We are passionate about supporting professional growth and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a midsized CRO allows you to have influence and impact when it matters most with support from direct line management.

To support continued growth from our clients, we are hiring all levels of CRAs experienced with oncology and rare disease across North America.

About you:

• 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.
• You take responsibility in the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.
• You have experience in study start up activities.

How you will spend your days as a CRA

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.).

As a CRA, 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.

Qualifications: CRA

• 4-year college degree or equivalent experience
• 2+ years CRA experience within the CRO or pharmaceutical industry to be considered for a CRA II. 4+ years of experience needed to be considered for a Sr. CRA position.  
• 1 year of Oncology monitoring experience, CAR-T preferred
• Availability for domestic travel including overnight stays, up to approximately …