Oversee site activation readiness, including preparation and submission of Clinical Trial Application Forms to Competent Authorities and Ethics Committees in compliance with regulations.
Manage collection of essential documents, customize informed consent forms, and coordinate translations to support study initiation.
Maintain communication with cross-functional teams and update project trackers and regulatory intelligence tools.

Qualifications:

Minimum: Bachelor's degree in life sciences or related field, or RN with 1+ years of regulatory or start-up experience in CRO/pharma.
Preferred: Advanced degree (MD, PhD, PharmD) or RAC certification, with experience in milestone tracking tools.
Skills: Strong communication, organizational skills, and proficiency in English; experience with spreadsheets and electronic mail required.

Precision for Medicine

Precision for Medicine is a Clinical Research Organization focused on precision medicine, combining novel clinical trial designs and advanced biomarker solutions, particularly in rare diseases and oncology. The company is growing and seeks dedicated professionals to support its mission, fostering a culture where employees feel appreciated and their ideas valued.

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