
201 - 500 Mitarbeiter
đ Pharmazie
đĽ Gesundheitswesen
đź Beratung
Pharmaceuticals ⢠Healthcare ⢠Consulting
Als auf Dermatologie spezialisierte CRO (Contract Research Organization) bieten wir wissenschaftliche Expertise, präzise Ergebnisse und hĂśchste Kundenzufriedenheit. Unser einzigartiges Leistungsangebot vereint spezialisierte Contract-Research-Services, fundierte Kenntnisse dermatologischer PrĂźfzentren in Nordamerika, Reichweite in Europa sowie die erweiterten Kapazitäten eines groĂen klinischen Forschungszentrums.
đ vor 11 Tagen
đŁď¸đşđ¸đŹđ§ Englisch erforderlich
Woher diese Stelle stammt
VerĂśffentlicht auf der Karriereseite von Innovaderm Research Inc., nicht Ăźber eine JobbĂśrse
Von Remote Rocketship zum ersten Mal gesehen vor 11 Tagen
Noch offen auf der Website von Innovaderm Research Inc.. GeprĂźft vor 1 Stunde.

201 - 500 Mitarbeiter
đ Pharmazie
đĽ Gesundheitswesen
đź Beratung
Pharmaceuticals ⢠Healthcare ⢠Consulting
Als auf Dermatologie spezialisierte CRO (Contract Research Organization) bieten wir wissenschaftliche Expertise, präzise Ergebnisse und hĂśchste Kundenzufriedenheit. Unser einzigartiges Leistungsangebot vereint spezialisierte Contract-Research-Services, fundierte Kenntnisse dermatologischer PrĂźfzentren in Nordamerika, Reichweite in Europa sowie die erweiterten Kapazitäten eines groĂen klinischen Forschungszentrums.
⢠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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