
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
🔥 13 minutes ago
Where this job comes from
Posted on Precision For Medicine's careers page, not through a job board
First seen by Remote Rocketship 13 minutes ago

1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
• Monitor and own the progress of clinical studies at investigative sites • Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and applicable regulations and standards • Coordinate activities required to set up and monitor studies • Identify investigators • Help prepare regulatory submissions • Conduct pre-study and initiation visits • Identify potential study risks and propose mitigation solutions • Prepare for investigator meetings, site visits, and project team updates • Handle conflicts using resolution strategies • Take responsibility for the quality and outcomes of work
• 4-year college degree or equivalent experience • More than 1 year of CRA experience within the CRO or pharmaceutical industry ideally • Oncology experience essential • Phase I experience desirable although not essential • First-In-Human (FIH) experience desirable although not essential • Availability for domestic travel, including overnight stays, up to approximately 50–60% travel commitment • International travel may be required for some senior-level positions • Fluency in English • Must be legally authorized to work in the country of employment without employer sponsorship
• Lower than average number of protocols • Reasonable travel and improved work/life balance • Direct line management support • Opportunities to provide input and have ideas valued and nurtured • Fully home-based working arrangement
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