Cra Ii

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pfm medical, inc.

πŸ“Remote - Belgium

Summary

Join Precision for Medicine, a unique CRO offering a supportive culture and excellent work-life balance. We integrate clinical trial execution with scientific knowledge and advanced data sciences. Our CRAs enjoy high retention rates due to manageable workloads and opportunities for professional growth. You will have a significant voice in a smaller CRO setting, allowing for greater influence and impact. We value our employees and foster a collaborative environment where your ideas are valued and nurtured. We are seeking a detail-oriented and problem-solving CRA with oncology experience.

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 for investigator meetings, site visits, or project team updates, 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

Benefits

  • Lower than average number of protocols, setting you up to be a protocol expert
  • Reasonable travel and improved work/life balance
  • Your voice will be heard and you will have influence and impact
  • Support from direct line management
  • Opportunities for professional growth
This job is filled or no longer available