Overview In this role you lead Phase I clinical projects for a single sponsor, ensuring on-time study delivery within budget and regulatory guidelines. You act as the primary liaison between the sponsor and our company, coordinating cross-functional
Overview Join UL’s Energy & Industrial Automation unit to lead certification projects that ensure safe, high-performing products for global markets. You will manage scope, timelines, and test programs, and contribute to UL requirement development. The role blends project leadership
Overview As IT Project Manager you own medium-to-high complexity IT initiatives, from platform rollouts to AI deployments, across multiple locations. You’ll manage plans, milestones, budgets and risk, coordinating internal teams and external partners to deliver on time
Overview In this role you will assess power generation equipment and assemblies for UL 2200/6200 certification and manage certification projects. You will work with cross-functional teams to determine scope, plan investigations, and coordinate testing, reviews, and communication
Overview In this role you will lead end-to-end meeting programs for Life Science clients, turning concepts into memorable events across destinations. You’ll coordinate cross-functional teams and partner with clients to ensure flawless execution, from venue sourcing
Overview As a Project Manager in Medical Writing, you lead and develop a capable team to deliver compliant, high-quality medical writing outputs within sponsor partnerships. You align with clinical development objectives and collaborate across functions to shape
Why join theHRdepartment? In our HR department, we play a critical role by ensuring that our teams are engaged, skilled, and aligned with the organization’s strategic goals. We anticipate changes in the business environment, foster a
Overview In this role you will lead the design and delivery of multi-country benefits financing programs for multinational clients, with a focus on UK, Europe and Asia and up to 30% international travel. You’ll work within
Overview As Engineering Lead you oversee a remote team of 5 engineers delivering complex AI and platform projects for enterprise clients. You own delivery from architecture to production, balancing technical leadership with people development. You work with
Overview In this role you drive regulatory strategy and submissions for multi-region studies, coordinating CTAs, regulatory applications, and trial milestones. You will lead cross-functional teams to ensure compliant, timely submissions and smooth study startup across EU
Overview In this role you coordinate investigator grants and contracting activities to support proposal development and trial initiation. You will maintain contracting systems, produce specialist contract language, and align with sponsor requirements and RSU plans. You’ll
Overview In this role you will oversee global payroll implementations and data migrations for Deel’s clients, guiding the end-to-end setup from onboarding to go-live. You’ll work cross-functionally with internal teams and clients to align payroll processes,
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview As a Senior Contract Associate, you drive the drafting, negotiation, and finalization of complex Clinical Site Contracts for clinical trials. You will serve as the liaison between CBO, GCO, Legal, sites, and external providers to
Overview In this role you lead the end-to-end management of indirect contracting for PDx International, guiding a team of contract specialists to ensure compliant distributor, wholesaler, and sales representative contracts. You drive governance, lean processes, and
Overview As a Clinical Research Associate, you oversee site qualification, initiation, monitoring, and close-out to ensure protocol and regulatory compliance across Germany. You work with cross-functional teams to safeguard data integrity, patient safety, and trial quality,
Overview As a CRA II for our multisponsor team in Germany, you oversee site performance and trial data integrity through monitoring and site management. You align with ICH-GCP, GPP and protocol requirements, liaising with site staff
Overview In this role you will contribute to the development and validation of coherent DSPs and transmission modules for optical networks within Nokia’s Optical Networks division. You will join a cross-disciplinary ASIC/SoC team focused on advancing
Overview In this Manager role you drive and supervise real-world evidence (RWE) projects for pharmaceutical and healthcare clients. You act as a trusted partner and primary client contact, ensuring timely delivery, scientific quality, and high satisfaction. You
Overview As a CRA for a single sponsor partnership in Germany, you will oversee site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. You will work with cross-functional teams to assess site