
1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
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.
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1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
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.
• Serve as primary point-of-contact and primary escalation point to the client • Coordinate and oversee all functional services including external vendors to the established timeline and budget • Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled appropriately. • Ensure functional areas are fully aware of the study scope and are managing the scope for their functional areas accordingly. • Manage the financial health of assigned studies, including oversight of project profitability, billable project hours, and compliance with on-time, accurate billing and forecasting to support business objectives. • Develop robust and comprehensive project plans, including timelines and proactive risk management to guide all parameters of trial execution with consistency and quality • Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and/or corrective and preventative action plans to address any quality findings. • Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation • Establish tracking metrics to monitor trial and team progress towards project goals • Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise • Lead both internal and client meetings and set expectations for the project team • Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues • Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project • Support business development and marketing activities as appropriate, including travel to Bid Defence meetings as required • Perform other duties as assigned by management • Remain compliant with organizational training, time-reporting and any other administrative duties as required • Provide ongoing feedback for functional team members including annual performance reviews • Ability to travel domestically and internationally including overnight stays
• Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 3-7 years of clinical research experience or proven competencies for this position and a minimum of 2-4 years of leading a project • Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trials • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS • Good communication and interpersonal skills to effectively interface with others in a team setting • Good organizational skills, attention to detail, and a customer service demeanor.
• Positive team culture • Flexible work arrangements • Professional development opportunities
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