Cra Ii

Summary

Join Precision for Medicine, a unique CRO offering a supportive and collaborative environment. We integrate clinical trial execution with scientific knowledge and advanced data sciences, resulting in high CRA retention rates. You'll enjoy a manageable workload, reasonable travel, and a strong work-life balance. Your contributions will be valued, and your voice will be heard. We offer opportunities for professional growth and impact within a smaller CRO setting. We are seeking a CRA with oncology experience and a commitment to quality.

Requirements

• College degree or equivalent experience
• At least 2 years independent on site monitoring experience within the CRO or Pharmaceutical industry
• Oncology experience is essential
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (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
• 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.)

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
• Find quick and creative ways of overcoming difficulties
• Impeccable eye for detail
• Identify potential study risks and propose solutions on how to mitigate them
• Take responsibility in the quality and outcomes of your work
• Adept at handling conflict by using tried and true resolution strategies

Benefits

• Lower than average number of protocols setting you up to be a protocol expert
• Reasonable travel and your work/life balance will benefit as a result
• Your voice will be heard
• Support from direct line management