Clinical Research Associate II

Summary

Join Precision for Medicine, a unique CRO prioritizing professional growth and boasting high CRA retention. We offer a supportive environment with reasonable travel and a focus on work-life balance. We are currently hiring CRAs of all levels with oncology monitoring experience. Your contributions will be valued, and you'll have a voice in a mid-sized company. We provide a competitive compensation package and a variety of benefits. Apply today and become part of our team dedicated to revolutionizing cancer treatment through precision medicine.

Requirements

• 4-year college degree or equivalent experience
• 2+ years CRA experience within the CRO or pharmaceutical industry to be considered for a CRA II
• 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

• 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.)
• Work with 2-3 protocols on average and support Project Managers with trials that are larger in scope
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Preferred Qualifications

• Calm, thoughtful, and responsive when things don’t go as planned
• Well-prepared, whether it be for an investigator meeting, site visit, or project team update, always staying two steps ahead of the game
• Able to find quick and creative ways of overcoming difficulties
• Impeccable eye for detail
• Able to identify potential study risks and propose solutions on how to mitigate them
• Takes responsibility in the quality and outcomes of your work
• Adept at handling conflict by using tried and true resolution strategies
• Experience in study start up activities

Benefits

• Paid time off
• Volunteer time off
• Robust medical offerings
• Non-vested 401k plus company match
• Paid parental leave
• Discretionary annual bonus
• Health insurance
• Retirement savings benefits
• Life insurance
• Disability benefits
• Parental leave
• Paid time off for sick leave and vacation