Associate Manager, Clinical Operations (m/w/d), Single Sponsor

Associate Manager, Clinical Operations (m/w/d), Single Sponsor page is loaded## Associate Manager, Clinical Operations (m/w/d), Single Sponsorlocations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob requisition id: R1503674We are currently looking for an **Associate Manager, Clinical Operations (m/w/d)** to work in a sponsor dedicated setting with one key client and **home-based throughout Germany**.In our *Clinical Functional Service Partnership* team, we work in a close partnership with our key customers to deliver comprehensive clinical trial management.Within this entry level role into Line Management, you will manage a team of CRAs/SrCRAs and maybe other roles like CTAs/CTCs in Germany. Furthermore, you will support interesting clinical trial projects of one pharma client and establish a collaboration with this sponsor.**While projects vary, your typical responsibilities might include:*** Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employee, and addressing employee relations issues and resolving problems.* Participate in the selection process for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained.* Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable.* Participate in the allocation of resources to clinical research projects by assigning staff based on their experience and training.* Manage the quality of assigned staff\’s clinical work through regular review and evaluation of work product.* Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.* Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.* May support experienced Managers with conducting review and analysis of assigned projects, including review of revenue recognition, project performance variances, contract opportunities and ad-hoc financial analysis as required.* May support with reviewing forecasting requirements from customer and completion of month end activities and providing global variance explanations to forecast.* May support with initiatives and workstreams to investigate and implement improvements to processes.* Support the collaboration with customer counterpart(s).**You should have:*** Bachelor’s or higher-level degree in life science.* At least **6 years clinical research experience, including CRA experience**.* **Mandatory experience in a line management secondment for at least 6 months.*** Fluent languages skills in **German on at least C1 level** and good command of English.* Full knowledge of drug development process.* Full knowledge of applicable **regulatory requirements, like ICH-GCP**.* Strong knowledge of financial management and resourcing.* Strong knowledge of Microsoft Office applications.* Effective communication, organizational, interpersonal, teamwork and leadership skills.* Ability to independently coordinate and manage new processes and to effectively prioritize tasks.* Positive attitude and ability to interact with all levels of staff and ability to lead and motivate teams.* Ability to establish and maintain effective working relationships with coworkers, managers and clients.* Flexibility to business travel and driving license.**What you can expect:*** Complex and interesting trials.* Highly motivated and cooperative team.* Leaders who support career growth.* Dynamic work environment that exposes you to new experiences.* Home-office, pension, accident insurance and more.Whatever your career goals, we are here to ensure you get there!**We invite you to join IQVIA.****Please apply with your English CV and motivation letter as well as your certificates and recommendation letters.**IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr