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Clinical Research Associate I or II
hace 1 semana
Precision for Medicine is not your typical CRO. We are passionate about nurturing our work environment and are proud to have exceptionally high CRA retention rates compared to industry standards.
At Precision for Medicine, CRAs are valued, enjoy their roles, and choose to stay because of our fantastic team and great quality of life. You will be assigned to one to two studies on average, allowing you to become an expert in study protocols. Travel is reasonable, ensuring a healthy work-life balance. Most importantly, your opinions will be listened to. Working in a smaller CRO gives you the opportunity to make a difference when it counts and receive support from your direct supervisors.
This role offers the flexibility of working fully from home in Madrid or Barcelona. We are specifically looking for a CRA I or CRA II.
About You:
- You remain composed, considerate, and proactive in handling unexpected situations.
- You are always well-prepared, whether it's for an investigator meeting, site visit, or project team update, staying ahead of the curve.
- You excel at finding quick and inventive solutions to challenges.
- Your attention to detail is impeccable.
- You can identify potential study risks and suggest effective solutions to mitigate them.
- You take ownership of the quality and results of your work.
- You are skilled at resolving conflicts using established strategies.
How We Support Your Development and Keep You Engaged:
You will oversee and manage the progress of clinical studies at research sites, ensuring that they are carried out, documented, and reported in accordance with protocols, SOPs, ICH-GCP, and all relevant regulations. You will coordinate all essential activities for study setup and monitoring (e.g., identifying investigators, assisting with regulatory submissions, conducting pre-study and initiation visits, etc.).
Qualifications:
Minimum Requirements:
- 4-year college degree or equivalent experience
Other Requirements:
- Experience as a CRA in the CRO or pharmaceutical industry; Minimum of 1 year of independent monitoring experience for a CRA I and at least 1.5 years for a CRA II.
- Background in Oncology
- Willingness to travel domestically with overnight stays, potentially up to 50-60% of the time (some senior roles may require international travel)
- Proficiency in English and, for non-English speaking locations, fluency in the local language
Preferred:
- Graduate or postgraduate degree with a focus on a scientific or healthcare field
The unique integrated approach at Precision enables the advancement of precision medicine through innovative clinical trial designs, top-tier operational and medical professionals, advanced biomarker and data analysis solutions, and a sincere dedication to rare diseases and oncology.
Precision medicine is transforming the fight against cancer—and we are committed to helping you leverage its capabilities. We target tumors on a molecular level using biomarkers to connect specific mutations with specific treatments. By merging profound scientific knowledge with sophisticated data from cutting-edge platforms, we apply specialized skills in crafting and executing targeted, adaptive clinical trials. Ultimately, we provide valuable insights that drive real-time decisions and optimize the path of oncology development.
Join us in exploring our expanding organization that serves clients dedicated to groundbreaking cancer treatments. We aim to ensure that our employees are recognized for their daily contributions. Your input will be welcomed, and your ideas will be embraced and fostered, leading to positive changes within the company.
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