
201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
đĽ 14 hours ago
Where this job comes from
Posted on Innovaderm Research Inc.'s careers page, not through a job board
First seen by Remote Rocketship 14 hours ago
Still open on Innovaderm Research Inc.'s site. Checked 1 hour ago.

201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
⢠Provide operational leadership for site contracting and budget negotiation activities across awarded clinical trials ⢠Lead and manage Site Budget & Contracting staff, including direction, coaching, development, workload oversight, and support ⢠Oversee site contracting and budget negotiation activities across the portfolio ⢠Provide oversight of Clinical Trial Agreements, financial exhibits, amendments, negotiation parameters, and country-specific requirements ⢠Establish and maintain contracting strategies, standards, and negotiation approaches ⢠Serve as the escalation point for complex or high-risk contract and budget negotiations ⢠Oversee implementation of study-specific site budgets, approval pathways, exceptions, and escalations ⢠Translate proposal-stage budget assumptions into study- and site-level budget and contracting strategies ⢠Collaborate with Legal Affairs, Project Management, Study Start-Up, Regulatory Affairs, Clinical Operations, Finance, and other stakeholders ⢠Provide site contracting expertise during proposal development ⢠Participate in bid defense meetings, client presentations, and sponsor strategy discussions ⢠Monitor portfolio-level contracting and budget performance and identify risks, delays, capacity constraints, and quality concerns ⢠Own and oversee Site Budget & Contracting business assets, templates, tools, intelligence, trackers, and reference materials ⢠Ensure data integrity and usability across applicable tools, trackers, and systems ⢠Lead process improvement, digital transformation, and automation initiatives ⢠Establish and monitor performance indicators and use operational data for continuous improvement ⢠Ensure staff training and consistent application of SOPs, processes, tools, and quality standards ⢠Partner with senior leadership on resource planning, functional priorities, process maturity, systems, quality, and improvement ⢠Foster accountability, collaboration, proactive risk management, knowledge sharing, and continuous improvement
⢠B.Sc. or in a relevant field of study ⢠5+ years of experience in clinical research, clinical trial budgeting, or related financial management roles within the pharmaceutical, biotech, or CRO industry ⢠Strong negotiation and communication skills ⢠Experience creating and maintaining budget templates tailored to global regions and therapeutic areas ⢠Experience representing the organization in bid defense meetings and client calls ⢠Technical proficiency maintaining pricing tools, cost databases, and budget models ⢠Leadership abilities to train and mentor junior specialists ⢠Demonstrated success partnering with senior team members to refine internal processes and improve deliverables ⢠Strategic thinking and experience contributing to process improvement initiatives ⢠Good knowledge of good clinical practices ⢠Knowledge of applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines ⢠Applicants must be legally able to work in Poland
⢠Permanent full-time position ⢠Vacation ⢠PPK ⢠Health allowance ⢠Home-based position with teleworking allowance ⢠Ongoing learning and development ⢠Attractive advancement opportunities ⢠Recruitment accommodations for applicants with disabilities, upon request
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