Data Management Lead I (Romania, Poland, UK, Hungary, Spain)

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values: Patients First, Quality, Respect, Empowerment & Accountability.

The DML I role can be based in Romania, Spain, Poland, UK, Hungary.

The Data Management Lead l provides leadership in all aspects of Data Management. Manages timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock. Collaboration with the relevant functions (Clinical, Biostatistics, Database Programming, Medical, Medical Writing etc.) across all geographies. Data Management’s single point of contact to ensure that the contracted Data Management deliverables are being met – specifically in terms of timeliness, financial management and quality.

The Data Management Lead l works under the guidance of their Line Manager and may receive additional direction/support from an experienced Data Management Lead or Subject Matter Experts. They may work as a co-DML with an experienced DML or work independently on less complex trials. QualificationsIdeal candidate will possess: Data Management experience in clinical research industry (CRO/Pharma). Proven record of coordinating and supporting project teams. Bachelor’s degree in a science or industry related discipline. Competent in written and oral English . Leadership skills that include: building and leading global (virtual) teams, ability to work effectively with and motivate virtual teams, ability to negotiate and influence in order to achieve mutually beneficial results, ability to conduct root cause analysis in business problem solving and process improvement development. Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards. Sound awareness of relevant regulations, including ICH-GCP, 21CRF11. Excellent technical skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, PMED, IVRS. Excellent interpersonal, oral and written communication skills. Excellent presentation skills. Strong customer focus, ability to interact professionally within a client organization. Basic knowledge of SAS. A little about us:

Parexel is proud to be a leading Clinical Research Organization, with colleagues committed to make a difference. As a member of our global team, you’ll have discussions in an open environment—sharing expertise, promoting learning, and getting to know one another on a personal level. You’ll also experience supportive management that encourages career growth through consistent performance discussions and evaluations.