Precision For Medicine

www.precisionformedicine.com

1 Job

1,710 Employees

About the Company

Precision for Medicine is an industry-leading global clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

Listed Jobs

Company Name: Precision For Medicine
Job Title: Clinical Research Associate II/ Senior Clinical Research Associate
Job Description: **Job Title:** Clinical Research Associate II / Senior Clinical Research Associate **Role Summary:** Responsible for monitoring oncology clinical trials in the Paris area, ensuring compliance with protocol, SOPs, ICH‑GCP, and regulatory standards. Manages study progress, coordinates site set‑up and monitoring visits, and provides oversight for clinical study operations. Senior CRAs additionally support larger trials, mentor junior staff, and contribute to client interactions and proposal development. **Expectations:** - Remain calm, proactive, and detail‑oriented when challenges arise. - Anticipate and mitigate study risks, delivering quality outcomes. - Balance independent site monitoring with effective collaboration with Project Managers and clients. **Key Responsibilities:** - Conduct site initiation, monitoring, and close‑out visits; review data, source documents, and regulatory compliance. - Coordinate study set‑up activities: investigator identification, regulatory submissions, and site onboarding. - Maintain accurate study records, progress reports, and visit logs. - Identify and propose risk mitigation strategies; manage resolutions of clinical trial issues. - Mentor and train junior CRAs; support knowledge transfer. - Engage with clients on study progress, propose payment processes, and contribute to proposal and presentation activities. - Travel domestically (with potential overnight stays); international travel possible for senior roles. **Required Skills:** - Clinical monitoring experience (1+ year) in oncology studies, preferably within a CRO or pharma environment. - Strong knowledge of ICH‑GCP, SOPs, and regulatory frameworks. - Excellent organizational, communication, and stakeholder management skills. - Ability to proactively identify risks, propose solutions, and manage conflicts. - Detail‑oriented with a rigorous approach to data quality and regulatory compliance. **Required Education & Certifications:** - Life sciences degree or equivalent scientific/healthcare experience. - Preferably a graduate or postgraduate degree in a scientific or healthcare discipline. - Two+ years of oncology clinical trial experience. - Experience with study start‑up activities is an advantage. - For Senior CRA roles, knowledge of financial management and mentoring experience is desirable. ---