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Key Responsibilities:
- Prepare and submit Clinical Trial Application forms and submission dossiers to Competent Authorities and Ethics Committees.
- Manage essential document collection, review, and quality control for site activation.
- Partner with CRAs and other functions to ensure site collaboration and timely activation.
Qualifications:
- Bachelor's degree in life sciences or related field, or equivalent experience.
- At least 1 year of regulatory or site start-up experience in a CRO or pharmaceutical/biotech industry.
- Strong communication and organizational skills, and fluency in English.
About the Company:
- Precision for Medicine is a CRO focused on integrating technology and scientific expertise to accelerate clinical trials.
- The company values innovation, collaboration, and a commitment to improving patient outcomes.
Precision for Medicine
Precision for Medicine is a clinical research organization (CRO) that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed and success rate of bringing therapies to patients, with a focus on Oncology and Rare Disease. It is a growing company with a culture of innovation and collaboration.