
1001 - 5000 employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
đ° $75M Private Equity Round on 2015-12
Healthcare âą Consulting âą 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.
đ„ 17 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
đ° $75M Private Equity Round on 2015-12
Healthcare âą Consulting âą 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.
âą Monitor and own the progress of clinical studies at investigative sites. âą Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. âą 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.).
âą Life science degree and / or equivalent experience âą 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. âą Site management or equivalent experience in clinical research. âą Experience managing oncology studies âą Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions) âą Excellent communication and organizational skills are essential. A team player. âą Evidence of a client focused approach âą Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment. âą Fluency in English and for non-English speaking countries the local language of country where position based.
âą Your voice will be heard. âą Strong focus on Oncology and Rare Disease. âą Remote based position with travel to sites for monitoring visits.
Apply Nowđ„ 17 minutes ago
Clinical Research Associate managing the progress of clinical studies remotely for Precision Medicine Group. Ensuring compliance with protocol, SOPs, and applicable regulations while coordinating site activities.
đ«đ· France â Remote
đ° $35.2M Venture Round on 2021-03
â° Full Time
đą Junior
đĄ Mid-level
đŹ Research Analyst
đ July 15
Clinical Research Associate executing clinical monitoring activities for oncology trials at BeOne. Ensuring compliance with ICH guidelines and collaborating with clinical operations teams.
đ«đ· France â Remote
đ” âŹ43k - âŹ53.7k / year
â° Full Time
đą Junior
đĄ Mid-level
đŹ Research Analyst
đŁïžđ«đ· French Required
đ July 1
Clinical Research Associate managing monitoring tasks and clinical studies at PSI. Ensuring high quality standards and supporting regulatory submissions in various therapeutic areas at PSI.
đ June 11
Clinical Research Associate at PSI responsible for onsite monitoring and study progress communication. Collaborating with internal teams and supporting regulatory preparations across clinical studies in various therapeutic indications.