
1001 - 5000 employees
Founded 2012
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 $35.2M Venture Round on 2021-03
Consulting • Healthcare • Logistics
Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.
🕒 September 21
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
Founded 2012
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 $35.2M Venture Round on 2021-03
Consulting • Healthcare • Logistics
Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.
• 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 • Handle appropriately sized clinical trials • Support larger clinical study teams • Train and mentor junior staff members • Interact directly with clients • Initiate payments • Participate in proposal activities, including development and client presentations
• 4-year college degree or equivalent experience • Holder of CRA certificate • Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment • Experience monitoring clinical trials across a variety of therapeutic areas • 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 and the local language is required • Additional languages considered an asset • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline preferred • Study start-up activities experience preferred • Understanding of financial management preferred for Senior CRAs
• Employees are empowered to make an impact • Meaningful client relationships • Career growth opportunities • Professional development • Collaborative environment • Quality-focused environment • Accountability-focused environment
Apply Now🕒 September 7
Clinical Data Manager leading data management across global clinical trials for ICON, a healthcare intelligence and clinical research organisation. Driving EDC builds, data review, vendor oversight, and database lock.
🕒 September 2
Project Manager leading feasibility and site activation for ICON’s global clinical research studies. Driving regulatory submissions, contracts, budgets, and cross-functional start-up delivery.
🕒 August 31
Senior Biostatistician leading clinical-trial biostatistics, statistical analysis plans, and study analyses. ICON advances medicines through global healthcare intelligence and clinical research.
🕒 August 26
Senior Clinical Data Manager leading sponsor-dedicated clinical data programs at Fortrea, a clinical trial services company. Overseeing CDM delivery, vendors, risks, standards, and client relationships.
🕒 August 25
Change Manager supporting global Clinical Data Management transformation initiatives at Fortrea. Coordinating stakeholder engagement, communications, readiness, training, and adoption activities.